Dynamin-like proteins (DLPs) are large GTPases that restructure membrane. DLPs such as the mitofusins form heterotypic oligomers between isoform pairs that bridge and fuse opposing membranes. In bacteria, heterotypic oligomerisation may also be important for membrane remodelling as most DLP genes are paired within operons. How DLPs tether opposing membranes is unknown. Here we show the crystal structure of a DLP heterotypic pair from the pathogen Campylobacter jejuni. A 2:2 stoichiometric tetramer is observed where heterodimers, conjoined by a random coil linker, assemble back-to-back to form a tripartite DLP chain with extreme flexibility. In vitro, tetramerisation triggers GTPase activity and induces lipid binding. Liposomes are readily tethered and form tubes at high tetramer concentration. Our results provide a direct mechanism for the long-range binding and bridging of opposing membranes by a bacterial DLP pair. They also provide broad mechanistic and structural insights that are relevant to other heterotypic DLP complexes.
Classical dynamins and dynamin-like proteins (DLPs) are an expansive family of mechano-chemical GTPases that induce membrane fission and fusion. In eukaryotes, their functional repertoire includes the scission of vesicles in clathrin-mediated endocytosis, mitochondrial membrane maintenance, and viral surveillance and sequestration1. In bacteria, the role of DLPs is poorly understood although a high level of functional diversification is emerging. During DNA replication, the Escherichia coli DLP CrfC ensures equipartitioning of the chromosome by coupling nascent DNA strands2. DynA and DynB in Streptomyces form part of the divisome super-assembly that implements cell division during sporulation3. LeoA in enterotoxigenic E. coli (ETEC) has a tentative role in heat-labile toxin release via outer membrane vesiculation4. While the DLP DynA in Bacillus subtilis forms foci at the inner membrane in response to environmental stress conditions5,6. DynA has in vitro membrane fusogenic activity, and therefore may act as a molecular suture to repair lipid bilayer. Such a phenotype is compatible with the Mycobacterium tuberculosis DLP IniA, which confers drug tolerance to the antibiotics isoniazid and ethambutol7. Common to all these bacterial DLPs, with CrfC the exception, is a known or speculated requirement for heterotypic complex formation for functional integrity. Indeed, most bacterial DLPs exist as side by side pairs within operons5,8. Streptomyces DynA and DynB interact together in vivo, while B. subtilis DynA is comprised of two DLPs genetically fused into a single unit. The presence of up to 8 putative DLPs in some cyanobacteria further suggests the potential for multicomponent heterotypic supercomplex formation, although only BDLP1 from Nostoc punctiforme9 has so far been characterised with a speculative role in the fusion of photosynthetic membranes.
The emerging significance of heterotypic DLP association in bacteria is reminiscent of mammalian mitofusin and OPA1 DLPs, which form homotypic and heterotypic oligomers between isoform pairs that drive mitochondrial membrane fusion. These families are increasingly linked to neurological dysfunction and neurodegeneration10,11,12. Mitofusin 1 and 2 are located on the mitochondrial surface where both are essential for membrane maintenance. The precise role for each mitofusin remains unclear with evidence for both distinct13 and cooperative membrane tethering and merging activity11,14. At the mitochondrial inner membrane, the OPA1 family form heterotypic complexes essential for cristae remodelling and fusion15. Long and short isoforms generate membrane anchored and soluble forms in the intermembrane space that complex together yet maintain distinct non-redundant roles16,17.
DLPs typically comprise 3 conserved structural motifs as described for BDLP1 from the cyanobacteria Nostoc punctiforme9. These include the GTPase domain (G-domain) and 4-helix neck and trunk domains. The neck and trunk correspond to the bundle signalling element (BSE) and stalk in eukaryotic systems, with HD1 and HD2 domain terminology used for the mitofusins (Fig. 1a). At the trunk tip is a lipid-binding domain that is modified for topological and functional tuning within the cell. In BDLP1, the lipid binding domain constitutes a paddle, which provides transient membrane attachment based on nucleotide state18. The mitofusins or OPA1 family have tip helices that provide permanent membrane attachment. For the mitofusin homologue Fzo1p, the equivalent transmembrane region protrudes into the intermembrane space19. Functional tuning also occurs by domain addition or omission20. Fzo1p has a poorly understood but functionally important N-terminal 190 amino acid (aa) domain21. Similarly, additional domains are common amongst bacterial DLPs8.
Emerging as fundamental to DLP-mediated membrane fission and fusion is a high level of inter-domain flexibility within the DLP subunit. BDLP1 nucleotide and lipid binding induces a 135° rotation from the closed to open conformation around hinge 1, and a 75° rotation from open to closed conformation around hinge 218 (Fig. 1a). Conformational changes around hinge 2 have been described in both classical dynamins and mitochondrial DLPs between the G-domain and bundle signalling element (BSE)22,23,24,25. There is also nascent evidence for conformational change around hinge 1 in eukaryotic DLPs16,21,26,27,28. The hinge regions and conformational changes described for BDLP1 are therefore emerging as conserved, albeit with modification, amongst many dynamin family members. However, the precise conformation relative to nucleotide state (or lipid binding) is not conserved amongst DLPs and instead appears tuned to specific membrane remodelling function and mechanism.
The recent partial structure of Mitofusin 1 showed the GTPase and HD1 domain to be in the BDLP1 hinge 2 open conformation26,29. Based on Asp189 forming an inter-domain tether, Mitofusin 1 is also predicted to fold at hinge 1 like BDLP126. Together the Mitofusin 1 and BDLP1 structures hint at a molecular mechanism for membrane fusion, where opposing membranes must be recruited, tethered, and brought into close apposition before physical merging30. How membrane tethering is initiated has been a long-standing question. An early model was based on the anti-parallel association of the mitofusin HR2 helix31. More recently it has been proposed that the HR2 helix might unfold from the HD1 and HD2 domains32. Alternatively, the partial Mitofusin 1 structure bound to GDP·AlF4¯ suggested tethering may occur via G-dimerisation26. This model is supported by atlastin membrane fusion models where G-dimerisation couples opposing membranes together33. In the case of Mitofusin 1 a tetramer may constitute the oligomeric state competent to tether membranes13. Similarly, no structural data is available for how heterotypic Mitofusin 1 and 2 complexes self-associate and orchestrate membrane fusion.
Given the mitofusins form functionally important homotypic and heterotypic oligomers between isoform pairs, and that bacterial DLPs may also require heterotypic oligomerisation for function, we searched for a bacterial DLP pair with which to probe the mechanism of heterotypic DLP-mediated membrane remodelling. Here we structurally and biochemically characterise the DLP pair from Campylobacter jejuni. We show how the DLPs oligomerise into a stoichiometric tetramer that comprises a highly dynamic tripartite chain. Combined with GTPase activity and lipid binding, we present a mechanism for how the tetramer tethers and bridges distantly opposing membranes. Ultimately, the tractability of bacterial systems makes them well suited for dissecting out the fundamental principles that underlie DLP-mediated membrane remodelling.
Campylobacter jejuni DLPs form a tetrameric complex
The dynamin-like genes cj0411 and cj0412 from Campylobacter jejuni share 24% sequence identity when aligned from the GTPase Switch 1 (Fig. 1b, c). cj0411 is a putative pathogenicity factor required for host colonisation34. The respective proteins, here called Cj-DLP1 (84.5 kDa) and Cj-DLP2 (71.2 kDa), were cloned, expressed and purified (Fig. 1d). Both DLPs are monomeric in solution and form a stable heterotypic tetramer, termed Cj-DLP1/2tetramer, with 2:2 stoichiometry when mixed (Fig. 1e).
The Cj-DLP1/2tetramer structure reveals a 2:2 ratio tetramer
Crystals of Cj-DLP1/2tetramer were obtained in the apo state and the structure solved (Table 1, Supplementary Fig. 1 and 2). As observed in solution, the asymmetric unit of Cj-DLP1/2tetramer comprises a heterotypic tetramer in 2:2 ratio (Fig. 2). Both Cj-DLP1 and Cj-DLP2 have a core DLP-like fold with GTPase, neck and trunk domains. The tetramer is dominated by a 2-fold symmetry where Cj-DLP2 with its symmetry mate (termed Cj-DLP2α and Cj-DLP2β) form a central back-to-back cis dimer flanked on each side by Cj-DLP1 (termed Cj-DLP1α and Cj-DLP1β). Crystals of Cj-DLP1/2tetramer bound to GDP and GDP·AlF4¯ (Table 1, Supplementary Fig. 3) were also obtained in the same P212121 space group as for the apo state. For both, the overall model is essentially identical to apo except for the coordination of GDP within the nucleotide binding pockets. Due to slightly lower resolution achieved, the GDP structure was not refined and reported. Within the GDP·AlF4¯ crystal, no density for the AlF4¯ moiety was observed. Based on the similarity between the GDP and GDP·AlF4¯ electron densities, it is understood that the GDP·AlF4¯ structure reported here is likely representative of the GDP conformation. Crystal packing rather than nucleotide state appears to dominate the conformation, as observed with the DLP atlastin in the presence of GDP33, and DNM1-L in the apo and GMPPNP bound state35.
Structural analysis of Cj-DLP2 within Cj-DLP1/2tetramer
With respect to Cj-DLP2, the trunk and neck are in an open conformation (Fig. 1a) and together form a linear series of 4-helix bundles. Similar architecture has been observed in the poorly understood DLP LeoA4 despite a low shared sequence identity of <20% (Fig. 3a). However, Cj-DLP2 and LeoA differ significantly in the conformation of their GTPase domains. For Cj-DLP2, hinge 2 exists in the closed position (Fig. 1a) so that the GTPase domain (G-domain) nucleotide-binding pocket is oriented orthogonal to the neck-trunk long axis. This arrangement is reminiscent of, and confirms, the cryo-EM modelled conformation of BDLP1 when self-assembled18. For LeoA, hinge 2 is in an open position so that a substantial screw-like rotation reorients the GTPase domain with the nucleotide-binding pocket facing outwards along the neck long axis (Fig. 3a). Taken together, Cj-DLP2 and LeoA appear to represent a bacterial DLP subtype now captured in two different conformational states. For the back-to-back cis Cj-DLP2 dimer, the dimerisation interface extends along each symmetry mate so that the GTPase, neck and trunk domains contribute to a substantial buried surface area of 5969 Å2. Removal of amino acids 348–401 and 509–542 within the trunk tip, to create Cj-DLP2∆trunk-tip, is sufficient to inhibit self-assembly via the dimerisation interface so that only Cj-DLP1/2 heterodimers assemble (Fig. 3b). This result, combined with the observation that the BDLP1 polymer utilises a similar back-to-back dimer (Fig. 3c)18, indicates that the crystallographic configuration of Cj-DLP2 homodimer is conserved and important for function.
Structural analysis of Cj-DLP1 within Cj-DLP1/2tetramer
Cj-DLP1 has a canonical BDLP1-like fold augmented with an N-terminal 119 amino acid globular domain that nestles between the neck and G-domains (Fig. 4a). As described later, this domain is essential for oligomerisation and is termed the assembly domain, or Cj-DLP1AD. Cj-DLP1 differs from the Cj-DLP2/LeoA subtype as its neck and trunk 4-helix bundles do not overlap and instead are linked by a distinct hinge 1 region within helices 21 and 26. Hinge 1 acts as a fulcrum with the trunks of Cj-DLP1α and Cj-DLP1β assuming significantly different conformations relative to each other. Cj-DLP1α forms an open linear conformation (Fig. 1a), whereas the Cj-DLP1β trunk is rotated in plane ~125° towards the neck C-terminus (Fig. 4b). While the trunk orientation is likely determined by crystal geometry here, the conformational variability reflects the flexibility of the hinge 1 neck-trunk interface. Importantly, such flexibility suggests that membrane will be sensed and bound by the lipid-binding domain at the trunk tip in almost any orientation relative to the neck and GTPase domain. Compared with Cj-DLP2, the G-domain of both Cj-DLP1α and Cj-DLP1β is rotated in-plane almost 90° around hinge 2. This open conformation (Fig. 1a) means that the nucleotide-binding pocket is oriented facing outwards along the neck long axis, and is similar to that observed for BDLP1 in the apo- or GDP-bound state9, and Mitofusin1 partial structures26,29. Importantly, full-length Cj-DLP1α represents the conformation predicted for Mitofusin 1 to tether opposing membranes upon G-dimer formation (Fig. 4c). These results, combined with the observation that the yeast mitofusin homologue Fzo1p36 has an N-terminal heptad repeat domain (HRN) of similar mass to Cj-DLP1AD, suggests Cj-DLP1α is a close respresentation of the mitofusin/Fzo1p class of DLPs.
Cj-DLP1/2tetramer oligomerisation mechanism
The structure of Cj-DLP1/2tetramer provides a mechanism for oligomerisation. The N-terminal 16 amino acids of Cj-DLP2 form helix 1 (Cj-DLP2H1), which inserts into a groove within Cj-DLP1AD (Fig. 5a). Here, Cj-DLP2H1 is partially clamped by Cj-DLP1 G-domain helix 18 and terminates in close proximity to Cj-DLP1 hinge 2, meaning it is ideally positioned to modulate Cj-DLP1 conformation upon binding. Truncation of either Cj-DLP2H1 or Cj-DLP1AD inhibits tetramer formation and results in monomer (Fig. 5b). This shows Cj-DLP2H1 and Cj-DLP1AD interaction to be essential for Cj-DLP1 and Cj-DLP2 heterodimerisation and subsequent tetramer formation. Within the Cj-DLP1/2tetramer asymmetric unit, the other potential oligomerization interface between Cj-DLP1 and Cj-DLP2 is the contact between Cj-DLP1AD and Cj-DLP2 at its neck and trunk interface (Supplementary Fig. 4a). However, given the limited contact area (494 Å2), the geometry of the P212121 space group with diametric arrangement of Cj-DLP1 symmetry mates, and the absence of heterodimer in the Cj-DLP2H1 truncation, this interface is considered a crystal packing contact only. Connection between the Cj-DLP2H1/Cj-DLP1AD complex and the bulk of Cj-DLP2 is therefore via a 9 amino acid random coil linker only (termed Cj-DLP2linker) (Fig. 5c). Such architecture suggests that Cj-DLP2linker represents a flexible tether in which Cj-DLP1α and Cj-DLP1β will be free to explore, in a mode akin to restricted Brownian motion37, a spectrum of positions and orientations relative to the central Cj-DLP2 dimer. Of significance is whether Cj-DLP2linker extends sufficiently to allow Cj-DLP1 and Cj-DLP2 G-domains to heterodimerise across the nucleotide-binding pocket interface. G-dimerisation is widely conserved in other DLPs and protein classes such as septins and represents a fundamental mechanism for increasing catalysis rate38. Molecular dynamics (MD) simulations modelling the movement of Cj-DLP1/2tetramer in solution show that Cj-DLP2linker is indeed sufficient to allow G-dimer formation between Cj-DLP1 and Cj-DLP2 (Fig. 5d, Supplementary Fig. 4b and Supplementary Movie 1). This in silico model is supported by in vitro GTPase activity assays. While individual Cj-DLP1 and Cj-DLP2 proteins show negligible GTP hydrolysis, Cj-DLP1/2tetramer at 1 µM concentration shows significant assembly-stimulated activity with a maximal observed hydrolysis rate of 3.6 µM/min (Fig. 5e). Mutations generated in both P-loops (Cj-DLP1/K175A and Cj-DLP2/K74A) or in individual P-loops within Cj-DLP1/2tetramer, show negligible GTP turnover (Fig. 5e and Supplementary Fig. 4c). This means that for Cj-DLP1/2tetramer, the GTP hydrolysis mechanism depends on heterotypic G-dimerisation between Cj-DLP1 and Cj-DLP2. Moreover, the presence of assembly stimulated GTP turnover specifically supports a model where catalysis is triggered by G-dimer formation across the nucleotide-binding pocket interface22 (Fig. 5f). G-dimerisation between, rather than within, discrete Cj-DLP1/2tetramer complexes should occur increasingly at higher protein concentrations when the effect of Cj-DLP2linker to maintain high local GTPase domain concentration becomes less relevant.
Cj-DLP1/2tetramer binds lipid in the absence of nucleotide
A direct role for membrane binding and remodelling was tested for in vitro. At 0.25–1 µM protein concentrations, spin assays show that Cj-DLP1 binds weakly to E. coli liposomes, while Cj-DLP2 exhibits negligible binding (Fig. 6a and Supplementary Fig. 5a). Increasing concentration to 10–20 µM shows equivalent lipid binding for both Cj-DLP1 and Cj-DLP2 although the binding efficiency remains relatively low (Supplementary Fig. 5b). For Cj-DLP2, the FVLF530-534EEEE mutation in the trunk tip inhibits lipid binding (Supplementary Fig. 5b) and suggests this region is the equivalent to the BDLP1 paddle. In contrast to individual Cj-DLP1 and Cj-DLP2 samples, Cj-DLP1/2tetramer shows efficient liposome binding at low concentration (0.5 µM). The addition of nucleotide including GTP, GMPPCP, and GDP has no obvious effect (Fig. 6a). Deletion of Cj-DLP1 amino acids 470–695 from Cj-DLP1/2tetramer to generate Cj-DLP1∆trunk/2tetramer (Fig. 6b) removes the predicted lipid binding region in the trunk tip and abrogates liposome binding (Fig. 6a and Supplementary Fig. 5b). At low concentration (0.5 µM), Cj-DLP1/2tetramer recruitment to the membrane is therefore mediated by Cj-DLP1.
Cj-DLP1/2tetramer remodels and tethers membrane
At high sample concentration (10–20 µM) and in the presence of liposomes, Cj-DLP1, Cj-DLP2 and Cj-DLP1/2tetramer form poorly ordered protein–lipid tubes ~40–50 nm in diameter that appear broadly similar in architecture (Fig. 6c). Liposome tubulation may be indicative of helical filament formation or the effect of protein crowding at high concentration. The addition of nucleotide had no obvious effect on the tube morphology. Working now at low concentration (0.5 µM), dynamic light scattering (DLS) was used to detect membrane tethering or fusion in vitro. The mixing of ~70 nm radius liposomes with Cj-DLP1, Cj-DLP2, or Cj-DLP1∆trunk/DLP2tetramer had no effect on average liposome size. In contrast, the mixing of Cj-DLP1/2tetramer, in the presence or absence of GTP, increased average liposome diameter at least 10-fold (Fig. 6d), which is indicative of liposome tethering and possibly fusion. This result was confirmed using fluorescent light microscopy where the same samples were mixed with liposomes incorporating 4% rhodamine-PE. While Cj-DLP1, Cj-DLP2, or Cj-DLP1∆trunk/DLP2tetramer samples yielded monodisperse proteoliposomes similar to native liposomes, those containing Cj-DLP1/2tetramer formed easily visible membrane clusters and aggregates (Fig. 6e). The equivalent samples were visualised by negative stain EM to similar effect (Supplementary Fig. 5c). Membrane aggregation was sufficiently efficient that sample thickness hindered visualisation by cryo-EM. Given such extensive membrane aggregation, it was unclear why membrane fusion was not subsequently readily detected by FRET based liposome mixing assays39. Overall, these data are indicative of liposome tethering at low concentration (0.5 µM) (Fig. 6f) and suggests Cj-DLP1/2tetramer drives membrane fusion rather than fission reactions.
The structure of Cj-DLP1/2tetramer provides a mechanism for heterotypic oligomerisation by a DLP pair triggered by the insertion of Cj-DLP2H1 into a groove within Cj-DLP1AD. Oligomerisation activates both Cj-DLP1 and Cj-DLP2 triggering significant assembly stimulated GTPase activity likely via G-dimerisation. While Cj-DLP1AD is specific to Campylobacter, the equivalent heterotypic coupling of two DLPs has been achieved in other bacterial species such as B. subtilis DynA by the head-to-tail fusion of a DLP gene pair5. This would have the effect of coupling a DLP pair by a short linker similar to the Cj-DLP1/2 heterodimer. DynA also oligomerises into a dimer capable of nucleotide independent tethering of liposomes5, which suggests that Cj-DLP1/2tetramer is structurally representative of this class of fused DLPs, which also includes Staphylococcus strains. Further studies in other bacterial systems are required to understand how extensively conserved heterodimeric coupling is. Many bacterial DLPs have gene modifications that include additional non-canonical DLP structural domains8 that might function similarly to Cj-DLP1AD. For example, the DLP gene neighbouring BDLP1 (uniprot B2IZD2) incorporates a DnaJ-like domain at its C-terminus that may act not only as a DnaK binding domain as its sequence predicts40, but also as an assembly domain to dimerise with BDLP1. The observation that Cj-DLP2 and Cj-DLP1 are inactive unless both are present may now explain why the structurally similar LeoA is inactive when monomeric and suggests that LeoA will indeed bind with LeoB and LeoC for activation and function4. Similarly, B. subtilis DynA requires both DynAD1 and DynAD2 GTPases to be functional for activation5.
In the absence of membrane stress, B. subtilis DynA localises uniformly at the inner membrane surface. In the presence of membrane pore forming agents such as nisin-like antibiotics or bacteriophage, DynA reorganises into punctate foci at the inner membrane where it is proposed to function as a fusogen in membrane maintenance and repair6. Recent striking images of phage endolysin-induced holes in the B. subtilis inner membrane41 confirm a critical cellular requirement for a fusogenic membrane repair machine capable of tethering and sealing distantly opposing membranes. Cj-DLP1/2tetramer has a cytosolic location within the Campylobacter cell (Supplementary Fig. 6) and a general membrane repair function is speculated as for B. subtilis DynA. The presence of an HcpA-like β-lactamase42 within the cj-dlp1/2 operon (Fig. 1b) suggests that β-lactam antibiotics as a source of cell envelope stress could be a trigger for membrane localisation. Alternative phenotypes are possible although a key role in cell division cytokinesis equivalent to Streptomyces DynA and DynB3 may tentatively be excluded. No obvious cell division defects were observed in a chromosomal knockout of cj-dlp1 and cj-dlp2 (Supplementary Fig. 6).
Our results provide a molecular model for how a bacterial heterotypic dynamin-like pair tethers membrane bilayers (Supplementary Fig. 7). In bacteria, which generally lack cytoplasmic organelles, opposing membranes are depicted as a pore within a single membrane as for DynA at the inner membrane6. The recruitment and binding of Cj-DLP1/2tetramer to membrane is nucleotide independent and is promoted by Cj-DLP1, which binds with higher avidity than Cj-DLP2. At low concentration, our data supports a model where Cj-DLP2 acts as an adaptor to couple two Cj-DLP1 subunits together and to markedly extend their membrane binding reach. This architecture combined with the inherent flexibility of Cj-DLP1/2tetramer provides a mechanism for distantly opposing membranes to be tethered in trans with a theoretical range of 40–45 nm when fully extended. The role of nucleotide for Cj-DLP1/2tetramer is unclear given membrane tethering and tubulation occurs in the absence of nucleotide, and its addition in vitro has no detectable effect under the conditions screened. However, the presence of assembly-stimulated nucleotide turnover, which requires both Cj-DLP1 and Cj-DLP2 GTPase domains to be active, strongly suggests nucleotide binding triggers hetero G-dimer formation. Localised concentration of Cj-DLP1/2tetramer on the membrane induces polymerisation and consequently membrane constriction akin to liposome tubulation. As local concentration increases, the degree to which G-dimerisation between neighbouring Cj-DLP1/2tetramer complexes occurs remains to be determined. Given the close structural homology of Cj-DLP1 with human Mitofusin 1 and the propensity of Cj-DLP1/2tetramer to tether membranes, it is likely that ultimately Cj-DLP1/2tetramer will mediate membrane fusion rather than fission reactions. A membrane fusion phenotype is also consistent with that proposed for B. subtilis DynA43. Nucleotide hydrolysis may be directly coupled to active fusogenic conformational changes within Cj-DLP1/2tetramer such as the arcing together of Cj-DLP1 and Cj-DLP2 neck and trunks as observed in the BDLP1 polymer18 and for Mitofusin 144, or their folding like a molecular staple9. These conformational changes may physically merge and fuse opposing membranes as suggested for Mitofusin 126. Alternatively, the spontaneous formation of Cj-DLP1/2tetramer protein-lipid tubes in vitro at high concentration suggests that membrane fusion may be driven passively as a consequence of induced membrane curvature18. In this case nucleotide hydrolysis may represent a mechanism to release Cj-DLP1/2tetramer from the membrane, as for BDLP1. The structure of Cj-DLP1/2tetramer also provides a natural mechanism for the bridging of opposing double membranes. In bacteria, double membrane systems might include inner membrane bulging induced by phage endolysin41, cell envelope vesiculation8 or the abscission of the cytokinetic septum during cell division. In structurally related eukaryotic DLP systems such as Fzo1p and the mitofusins, full length oligomerised structures are required to determine whether the Cj-DLP2 homodimer arrangement is conserved across evolutionary domains.
Cj-DLP1 is a BDLP1-like subtype with a distinct and highly flexible hinge 1 region between neck and trunk 4-helix bundles. The conformation of Cj-DLP1, with hinge 1 and hinge 2 open, is different to those previously observed for BDLP1. The structure is important as it represents the predicted conformation required for DLPs to bridge opposing membranes through G-dimerisation. Given the similarity of Cj-DLP1 to Mitofusin 1 partial structures, it therefore supports a mitochondrial membrane tethering model based on G-dimerisation26 rather than the anti-parallel association31 and the unfolding32 of the HR2 helix. The structure is also reminiscent of the conformation of Dynamin 1 when polymerised and bound to GMPPCP, which has so far has only been described from structures fitted as rigid bodies into cryo-EM filament reconstructions45.
Cj-DLP2 has closer structural similarity to the ETEC DLP LeoA than Cj-DLP1 and BDLP1. Distinguishing features include overlapping neck and trunk domains with a reduced hinge 1 region. While this architecture does not preclude hinge 1 closing, the overlapping neck and trunk suggests the potential for less flexibility compared with Cj-DLP1, BDLP1 and Dynamin 1. The incorporation of Cj-DLP2 into a back-to-back dimer means any hinge 1 closure would likely require dimer dissociation or significant conformational rearrangement. MD simulations also suggest that heterotypic G-dimerisation may only occur when hinge 2 is in, or near, the closed position due to the geometric constraints of Cj-DLP2linker (Fig. 5f). However, this does not limit the Cj-DLP2 GTPase domain from forming a LeoA-like open conformation during periods of the nucleotide hydrolysis cycle when not G-dimerised. Whether Cj-DLP2 structure is representative of Mitofusin 2, with neck and trunk arrangements closer to LeoA, remains to be determined. Minimally, the Cj-DLP2 structure with hinge 1 open and hinge 2 closed reflects the conformation of full-length Mitofusin 1 when bound to GDP.BeF344. A similar conformation has previously been shown for polymerised BDLP1 when bound to GMPPNP18. For both Cj-DLP2 and BDLP1 a back-to-back dimer is observed when oligomerised (Fig. 3c), which raises the question as to whether either Mitofusin 1 or Mitofusin 2 will utilise a similar dimerisation interface. Cj-DLP2 exists as a monomer in solution rather than as the back-to-back dimer. Such Cj-DLP2 self-assembly autoinhibition may be mediated by Cj-DLP2H1, which in the absence of Cj-DLP1AD may bind in cis across part of the dimerisation interface and sterically hinder self-assembly. However, as truncation of Cj-DLP2H1 yields a monomeric species and does not form dimer (Fig. 5b), it may be that a Cj-DLP2 conformational change, such as hinge 1 closure, ultimately mediates self-assembly autoinhibition.
Bacterial DLPs usually exist as at least a genetic pair within operons, and our data suggests that heterotypic pairing in bacteria is fundamental for function. Our results show a novel mechanism for oligomerisation within the dynamin family, one that facilitates the long-range recruitment and tethering of membranes. They provide a molecular context for how other bacterial DLP pairs such as B. subtilis DynA may operate. In addition, the structure of Cj-DLP1 is important as it shows high structural homology to Mitofusin 1, for which there is currently no full-length structure. The Cj-DLP2 structure is similar to ETEC LeoA but in an alternative conformation. The Cj-DLP2 homodimer arrangement is equivalent to polymerised BDLP1 dimers18. BDLP1 also has close structural homology to Mitofusin 1. Cj-DLP1 and Cj-DLP2 therefore unify multiple bacterial and eukaryotic DLP systems, and represent an important snapshot into the type of conformations and oligomerisation mechanisms that will likely be fundamental for DLP-mediated membrane fusion.
Cloning, protein expression and purification
The cj-dlp1 gene (cj0411) from Campylobacter jejuni was cloned into pHis17 vector (pET derivative), encoding the full-length protein with a C-terminal hexahistidine tag. The cj-dlp2 gene (cj0412) from C. jejuni was cloned into pOPTM vector (pET derivative), which encodes an N-terminal MBP fusion with a TEV cleavage site in the linker and a C-terminal hexahistidine tag. Overexpression of cj-dlp1 and cj-dlp2 was achieved in E. coli BL21 (DE3) cells induced with 1 mM IPTG at 18 °C overnight. Cells were harvested by centrifugation, flash frozen in liquid nitrogen and stored at −80 °C. A list of all primers used in this study is shown in Supplementary Table 1.
For purification of Cj-DLP1, cells were lysed by sonication in 50 mM Tris pH 8.0 and 1 M NaCl. The cell lysate was centrifuged in a Ti45 rotor (Beckman Coulter) at 98,000 × g at 4 °C for 45 min. The supernatant was loaded onto 2 × 5 ml HisTrap columns (GE healthcare) at 4 °C. The column was washed and eluted with the addition of 300 mM imidazole pH 8.0 to the wash buffer. 5 mM DTT was added immediately into the elution peak. The protein was gel filtrated using a HiPrep 26/60 Sephacryl S300 column (GE healthcare) in buffer TEN 7.5 (20 mM Tris pH 7.5, 1 mM EDTA, 1 mM sodium azide) containing 1 mM DTT. Fractions were concentrated to ~10 mg/ml, flash frozen in liquid nitrogen and stored at −80 °C.
For purification of Cj-DLP2, cells were lysed in 50 mM Tris pH 9.0, 1 M NaCl, 2 mM DTT and 2 mM EDTA. The lysate was centrifuged as described above and the supernatant loaded onto a self-packed column with ~10 ml of amylose resin (New England Biolabs). The column was washed with 50 mM Tris pH 9.0, 0.5 M NaCl, 1 mM DTT, 1 mM EDTA and 20% glycerol. The sample was eluted by the addition of 10 mM maltose to the wash buffer. The MBP was cleaved by TEV protease and the products separated by gel filtration using a HiPrep 26/60 Sephacryl S300 column in buffer TEN 7.5 containing 1 mM DTT. Fractions were concentrated to ~10 mg/ml, flash frozen in liquid nitrogen and stored at −80 °C.
For purification of Cj-DLP1/2tetramer, purified Cj-DLP1 and Cj-DLP2 were mixed at equal molar ratio and incubated at 4 °C for 30 min. The resulting product was gel filtrated with a HiPrep 16/60 Sephacryl S300 column in buffer TEN 7.5 containing 1 mM DTT. Fractions were concentrated to ~10 mg/ml, flash frozen in liquid nitrogen and stored at −80 °C.
Selenomethionine labelled proteins were overexpressed in B834 (DE3) cells (methionine auxotrophic) in SelenoMethionine Medium (Molecular Dimensions) and were purified as for native.
Using the wild type Cj-DLP1 or Cj-DLP2 expression plasmid as the template, point mutations and truncations of cj-dlp1 or cj-dlp2 were carried out using one-step isothermal DNA assembly (Gibson assembly)46. All mutants and truncations were expressed and purified as for native.
Protein crystallisation and cryoprotection
In total 10 mg/ml Cj-DLP1/2tetramer was incubated with 3 mM MgCl2, 2 mM GDP, 2 mM AlCl3 and 20 mM NaF (abbreviated as GDP·AlF4−) for 30 min at room temperature. Equal volumes of the protein and the crystallisation solution (0.8 M succinate pH 7.0) were mixed to set up sitting-drop vapour diffusion at 20 °C. Initial crystals were harvested into 0.5 ml of reservoir solution containing GDP·AlF4¯, followed by vortexing with MicroSeed Beads (Molecular Dimensions). This seed crystal stock was aliquoted, flash frozen in liquid nitrogen and stored at −80 °C. For obtaining Cj-DLP1/2tetramer GDP·AlF4¯ crystals, the seed stock was diluted 1:100 into a pre-mixed protein-reservoir drop containing 0.7–1.0 M succinate pH 7.0 and GDP·AlF4¯. Crystals appeared overnight and were harvested after one week at 20 °C. For obtaining Cj-DLP1/2tetramer apo crystals, the Cj-DLP1/2tetramer GDP·AlF4¯ seeds were diluted 1:50 into a pre-mixed protein-reservoir drop containing 0.7–1.0 M succinate pH 7.0 only. Crystals obtained were then used to make a new apo seed stock with the same reservoir solution. The new apo seeds were used to grow Cj-DLP1/2 apo crystals. Iterative rounds of seed preparation from newly grown crystals did not improve the diffracting power of either the apo or GDP·AlF4¯ crystals. Selenomethionine crystals were similarly prepared except using selenomethionine labelled sample. Successful cryogenic protection required a slow iterative addition of glucose to the crystallisation drop, up to 60% final concentration. The succinate concentration ± GDP·AlF4¯ was maintained throughout. Crystals were harvested and flash frozen in liquid nitrogen.
Data collection and structure determination
Diffraction data were collected at 100 K at Diamond Light Source, UK. A SAD dataset was collected from a single crystal. One line scan dataset was collected from a single Cj-DLP1/2 apo crystal. XDS47 and Aimless48 were used for data integration and scaling. For GDP·AlF4¯ incorporated crystals, line scan was used to collect multiple datasets of small wedges at various positions within each crystal. XDS was used to process and integrate each dataset. Blend49 was used to analyse the degree of isomorphism among different datasets. Utilising Aimless, nine wedge datasets from two different crystals were merged and scaled together.
Using the SAD dataset, an initial 6 Å resolution electron density map was generated by Phenix AutoSol50. Initially, 26 selenomethionine sites from 28 were identified. Using Phenix, non-crystallographic symmetry averaging with phase extension against higher resolution native datasets followed by density modification generated a map of sufficient quality for initial poly-alanine model building. Combined MR-SAD with the poly-alanine model allowed the identification of 27 selenomethionine sites from the SAD dataset. A new round of phase extension and density modification resulted in an improved map with good side chain detail. Iterative rounds of model building and refinement were then carried out with Coot51, Phenix, and Refmac552. Phenix_rosetta refinement53 was used to improve model geometry. The density for Cj-DLP1α hinge 1 region and trunk does not show side chain detail but is of sufficient quality to allow almost continual poly-alanine main chain to be built with confidence (residues 466–703 with chain breaks at 506–514 and 626–629). Selenomethionine residue 654 allowed unambiguous location and orientation of the trunk 4-helix bundle. To aid model building in this region a homology model based on the crystal structure of the BDLP1 (PDB ID 2J69) trunk domain was used as a template. The density for Cj-DLP1β hinge 1 region and trunk is of lower quality but sufficient for unambiguous location of the trunk 4-helix bundle motif. Here, the Cj-DLP1α trunk model was rigid body fitted and regions with no supporting electron density removed. 90.4% of all residues are positioned within the favoured region of the Ramachandran plot with 0.74% outliers. For the GDP·AlF4¯ dataset, the GDP coordinates were manually fitted into the Fo–Fc density in Coot and refined. No clear density was observed for the AlF4¯ moiety. For the GDP·AlF4¯ model, 90.6% of all residues are positioned within the favoured region of the Ramachandran plot with 0.94% outliers.
To determine the mass of protein samples, an Agilent 1260 equipped with miniDAWN TREOS light scattering detector and an Optilab T‐rEX refractive index detector (Wyatt Technologies) was used. 100 μl protein samples at 1–2 mg/ml were injected onto a Superdex 200 10/300 GL column (GE Healthcare) equilibrated in TEN 7.5, 1 mM DTT. Data were analysed using the ASTRA software (Wyatt Technologies).
E. coli whole cell lipid (Avanti Polar Lipids) was used to make liposomes. For making fluorescent liposomes, rhodamine-PE (Thermo Scientific) was mixed with E. coli whole cell lipid in a molar ratio of 4:96 in chloroform. A nitrogen stream was used to evaporate the chloroform and the lipid film then dried under vacuum for 3 h. The lipid film was subsequently re-suspended in 20 mM HEPES pH 7.2, 100 mM NaCl and 1 mM DTT (termed reaction buffer). The resulting two-phase mixture was sonicated and then extruded using a polycarbonate membrane with pore size 0.2 μm (Mini-Extruder, Avanti Polar Lipids).
Cj-DLP1, Cj-DLP2 or Cj-DLP1/2tetramer samples at the desired concentration were incubated ± 0.3 mg/ml E. coli whole cell liposomes in reaction buffer at room temperature for 30 min. 3 mM MgCl2 and 2 mM nucleotide (GDP, GTP, GMPPCP, GMPPNP) were added accordingly. Reactions were spun in a TLA 100 rotor (Beckman Coulter) at 20 °C for 20 min at 100,000 × g using an Optima TLX100 ultracentrifuge (Beckman coulter). Supernatants and pellets were analysed by SDS–PAGE, followed by silver staining (SilverQuestTM Silver Staining Kit, Invitrogen). All experimental conditions were repeated at least twice.
EM analysis of Cj-DLP1/2 mixed with liposomes
0.5–20 μM Cj-DLP1, Cj-DLP2 or Cj-DLP1/2tetramer samples were mixed with 0.3–1 mg/ml E. coli whole cell liposomes at room temperature for up to 4 h. The samples were applied to glow-discharged, 400-mesh carbon coated copper grids and stained with 2% uranyl acetate. Images were recorded on a CM200 (Philips) and T12 Spirit equipped with 4 K CCD camera.
Liposome tethering assay
The DLS tethering assay was carried out as described for atlastin54. Zetasizer (Malvern) was used with default settings to determine liposome size in solution. 1 μM Cj-DLP1, Cj-DLP2 or Cj-DLP1/2tetramer samples were mixed with 40 μl 0.3 mg/ml E. coli whole cell liposomes at room temperature. 3 mM MgCl2 and 2 mM GTP were added as required. The same samples were also visualised by fluorescent microscopy using a Leica DMi8 with ×40 objective and a DFC365 FX camera. Liposomes had 4% rhodamine-PE incorporated. After 30 min incubation at room temperature, the samples were spotted onto a glass coverslip and imaged. All experimental conditions were repeated at least twice.
For analysing GTPase activity, 2 μM Cj-DLP1 and Cj-DLP2 samples, or 1 μM Cj-DLP1/2 tetramer complexes were used. Reactions at 37 °C were carried out in the reaction buffer and initiated via the addition of 1 mM GTP and 2.5 mM MgCl2, and quenched with the addition of 0.1 M EDTA pH 8.0. Free phosphate concentration was determined using a malachite green based kit (PiColorLockTM Gold Phosphate Detection System, Innova Biosciences).
Campylobacter growth and gene knockout
Wild type C. jejuni 81–176 were grown on MH agar under micro-aerobic conditions using CampyGen sachets (Oxoid) at 37 °C, as described previously55. For knockout of cj-dlp1 (cj0411) and cj-dlp2 (cj0412) genes from the C. jejuni chromosome, the whole operon including cj0411, cj0412 and cj0413 (4710 base pairs) were amplified by PCR and inserted into the MCS site of pUC19 to create pUC19_cj0411-13. Using PCR and Gibson assembly, base pairs 300–3980 from the 5′ end of cj0411, cj0412 and cj0413 operon were excised from pUC19_cj0411–13 and replaced by a kanamycin resistance cassette. Within the operon, cj0413 initiates at base pair 4006 meaning this gene is unaffected by the kanamycin resistance cassette insertion. The resulting plasmid pUC19_∆cj-dlp1/2 was electroporated into wild type C.jejuni 81–17655 and plated onto MH agar containing 50 μg/ml kanamycin. The desired knockout, called ∆cj-dlp1/2, was verified by colony PCR and sequencing, and stored in MH media supplemented with 15% glycerol at −80 °C.
Subcellular fraction assay
Subcellular fraction of C. jejuni was performed as described previously with small modifications56. In brief, freshly grown cells in MH media were harvested and washed by PBS. For generating periplasmic and cytoplasmic fractions, cells were incubated with PBS buffer containing 1 mg/ml polymyxin B sulphate and 5 mM EDTA at 4 °C for 1 h. After centrifugation at 4 °C at 16,000 × g for 30 min, the spheroblasts were pelleted. The supernatant was removed and centrifuged again for 30 min at 16,000 × g. The resulting supernatant represents the periplasmic fraction. The spheroplasts were resuspended in PBS and disrupted by Lysing Matrix B (MPbio) on FastPrep-24 5 G Homogenizer (MPbio). After spinning at 12,000 × g for 5 min to remove unbroken cells, the sample was centrifuged at 150,000 × g at 4 °C for 1 h to pellet the membranes. The supernatant was further centrifuged at 150,000 × g at 4 °C for 30 min, resulting in soluble cytoplasmic fraction. For inner membrane and outer membrane fractions, the pellets were incubated with PBS containing 1% N-lauroylsarcosine sodium at room temperature for 1 h. The sample was centrifuged for 1 h at 4 °C at 150,000 × g, resulting in soluble inner membrane and insoluble outer membrane fractions.
Each fraction with equivalent cell numbers were analysed by SDS-PAGE. iBlot dry blotting system (Invitrogen) was used to transfer proteins from SDS-PAGE to membrane. To generate antisera of HcpA, the cj0413 gene was cloned into pHis17 vector with a C-terminus 6 x His tag, expressed and purified through refolding as described42. Antisera against Cj-DLP1, Cj-DLP2 and HcpA (cj0413) were raised in rabbit respectively (Cambridge Research Biochemicals). Antisera against RpoA, MotA and FlgP Campylobacter jejuni were generous gifts from David Hendrixson, UT Southwestern Medical Center. The α-Cj-DLP1, α-Cj-DLP2, α-HcpA, α-RpoA, α-MotA, α-FlgP polyclonal antisera were diluted 1:2000, 1:500, 1:3000, 1:2000, 1:5000, 1:20,000, respectively. After washing, rabbit, mouse, or guinea pig HRP conjugated secondary antibody was used according to manufacture protocol. Blots were developed using Luminata Crescendo Western HRP Substrate (Millipore) and visualised using a ChemiDoc MD station (BioRad).
Hetero G-domain dimer model: a candidate Cj-DLP1/2 G-domain heterodimer was created by aligning Cj-DLP1 and Cj-DLP2 onto different chains of the Mitofusin 1 G-domain homodimer (5GOM) using FATCAT. The resulting fit had no overlapping atoms and was relaxed in explicit solvent with CHARMM26 for 10 nanoseconds. The resulting heterodimeric structure was used to define the attractive interface contacts between G-domain heterodimers via the Shadow definition57 to be used in the structure-based potential.
Structure-based potential: The structure-based model (SBM) is a protein simulation potential energy function based on the energy landscape theory of protein folding58. Here, the SBM was generated using the SMOG v2.0.3 software package (http://smog-server.org)59 with the ‘SBM_Calpha+gaussian’ forcefield60. The native structure was Cj-DLP1/2tetramer with GDP·AlF4¯. Cj-DLP1 trunk domains were removed and a linking loop added between M463 and N705 using SWISS-MODEL. The crystal contact between Cj-DLP1AD and Cj-DLP2 at its neck and trunk interface (Supplementary Fig. 4a) was removed. The protein was represented as a single bead per residue at the position of the Calpha carbon. Stable heterodimerisation between G-domains was made possible by additionally including the interface contacts determined from the hetero G-domain dimer model as short-range attractive interactions. Making them half as strong as the native interactions populated the heterodimerised configuration 50% of the time during the simulation.
Molecular dynamics (MD) simulations: The accessibility of heterodimerisation was determined through MD simulations of the SBM. The simulations were performed with Gromacs v4.5.3 modified to include the Gaussian contact potential (available at http://smog-server.org). Simulation was performed using reduced units, a time step of 0.0005, and a Langevin thermostat with a coupling constant of 1. The reduced temperature was 0.92, a temperature low enough to prevent unfolding of the individual proteins, but high enough to sample reversible heterodimerisation. The trajectory used to create the free energy surface in Fig. 5d corresponds to 5 × 109 time steps. In addition 5 × 107 time steps are detailed in Supplementary Fig. 4b. The reaction coordinate is the distance between the centres of mass of the respective GDP molecules, which is <2 nm in the docked heterodimer. Also monitored is the fraction of heterodimeric contacts included as stabilising interactions that are within 120% of their distance in the modelled Cj-DLP1/2 heterodimer.
The atomic coordinates have been deposited in the Protein Data Bank (PDB) under accession codes 5OWV (Cj-DLP1/2tetramer apo) and 5OXF (Cj-DLP1/2tetramer GDP·AlF4¯).
Praefcke, G. J. & McMahon, H. T. The dynamin superfamily: universal membrane tubulation and fission molecules? Nat. Rev. Mol. Cell Biol. 5, 133–147 (2004).
Ozaki, S. et al. A replicase clamp-binding dynamin-like protein promotes colocalization of nascent DNA strands and equipartitioning of chromosomes in E. coli. Cell Rep. 4, 985–995 (2013).
Schlimpert, S. et al. Two dynamin-like proteins stabilize FtsZ rings during Streptomyces sporulation. Proc. Natl Acad. Sci. USA 114, E6176–E6183 (2017).
Michie, K. A., Boysen, A., Low, H. H., Moller-Jensen, J. & Löwe, J. LeoA, B and C from enterotoxigenic Escherichia coli (ETEC) are bacterial dynamins. PLoS ONE 9, e107211 (2014).
Burmann, F., Ebert, N., van Baarle, S. & Bramkamp, M. A bacterial dynamin-like protein mediating nucleotide-independent membrane fusion. Mol. Microbiol. 79, 1294–1304 (2011).
Sawant, P., Eissenberger, K., Karier, L., Mascher, T. & Bramkamp, M. A dynamin-like protein involved in bacterial cell membrane surveillance under environmental stress. Environ. Microbiol. 18, 2705–2720 (2015).
Colangeli, R. et al. The Mycobacterium tuberculosis iniA gene is essential for activity of an efflux pump that confers drug tolerance to both isoniazid and ethambutol. Mol. Microbiol. 55, 1829–1840 (2005).
Bohuszewicz, O., Liu, J. & Low, H. H. Membrane remodelling in bacteria. J. Struct. Biol. 196, 3–14 (2016).
Low, H. H. & Löwe, J. A bacterial dynamin-like protein. Nature 444, 766–769 (2006).
Ranieri, M. et al. Mitochondrial fusion proteins and human diseases. Neurol. Res. Int. 2013, 293893 (2013).
Detmer, S. A. & Chan, D. C. Complementation between mouse Mfn1 and Mfn2 protects mitochondrial fusion defects caused by CMT2A disease mutations. J. Cell. Biol. 176, 405–414 (2007).
Zuchner, S. et al. Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A. Nat. Genet. 36, 449–451 (2004).
Ishihara, N., Eura, Y. & Mihara, K. Mitofusin 1 and 2 play distinct roles in mitochondrial fusion reactions via GTPase activity. J. Cell Sci. 117, 6535–6546 (2004).
Chen, H. C. et al. Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development. J. Cell. Biol. 160, 189–200 (2003).
Frezza, C. et al. OPA1 controls apoptotic cristae remodeling independently from mitochondrial fusion. Cell 126, 177–189 (2006).
DeVay, R. M. et al. Coassembly of Mgm1 isoforms requires cardiolipin and mediates mitochondrial inner membrane fusion. J. Cell. Biol. 186, 793–803 (2009).
Zick, M. et al. Distinct roles of the two isoforms of the dynamin-like GTPase Mgm1 in mitochondrial fusion. FEBS Lett. 583, 2237–2243 (2009).
Low, H. H., Sachse, C., Amos, L. A. & Löwe, J. Structure of a bacterial dynamin-like protein lipid tube provides a mechanism for assembly and membrane curving. Cell 139, 1342–1352 (2009).
Fritz, S., Rapaport, D., Klanner, E., Neupert, W. & Westermann, B. Connection of the mitochondrial outer and inner membranes by Fzo1 is critical for organellar fusion. J. Cell. Biol. 152, 683–692 (2001).
Low, H. H. & Löwe, J. Dynamin architecture - from monomer to polymer. Curr. Opin. Struc. Biol. 20, 791–798 (2010).
De Vecchis, D. et al. A membrane-inserted structural model of the yeast mitofusin Fzo1. Sci. Rep. 7, 10217 (2017).
Chappie, J. S., Acharya, S., Leonard, M., Schmid, S. L. & Dyda, F. G domain dimerization controls dynamin’s assembly-stimulated GTPase activity. Nature 465, 435–440 (2010).
Faelber, K. et al. Crystal structure of nucleotide-free dynamin. Nature 477, 556–561 (2011).
Ford, M. G. J., Jenni, S. & Nunnari, J. The crystal structure of dynamin. Nature 477, 561–566 (2011).
Mattila, J. P. et al. A hemi-fission intermediate links two mechanistically distinct stages of membrane fission. Nature 524, 109–114 (2015).
Cao, Y. L. et al. MFN1 structures reveal nucleotide-triggered dimerization critical for mitochondrial fusion. Nature 542, 372–377 (2017).
Chen, Y. et al. Conformational dynamics of dynamin-like MxA revealed by single-molecule FRET. Nat. Comms. 8, 15744 (2017).
Frohlich, C. et al. Structural insights into oligomerization and mitochondrial remodelling of dynamin 1-like protein. EMBO J. 32, 1280–1292 (2013).
Qi, Y. B. et al. Structures of human mitofusin 1 provide insight into mitochondrial tethering. J. Cell. Biol. 215, 621–629 (2016).
Daumke, O. & Roux, A. Mitochondrial homeostasis: how do dimers of mitofusins mediate mitochondrial fusion? Curr. Biol. 27, R353–R356 (2017).
Koshiba, T. et al. Structural basis of mitochondrial tethering by mitofusin complexes. Science 305, 858–862 (2004).
Franco, A. et al. Correcting mitochondrial fusion by manipulating mitofusin conformations. Nature 540, 74–79 (2016).
Byrnes, L. J. & Sondermann, H. Structural basis for the nucleotide-dependent dimerization of the large G protein atlastin-1/SPG3A. Proc. . Natl Acad. Sci. U. S. A. 108, 2216–2221 (2011).
Novik, V., Hofreuter, D. & Galan, J. E. Identification of Campylobacter jejuni genes involved in its interaction with epithelial cells. Infect. Immun. 78, 3540–3553 (2010).
Wenger, J. et al. Functional mapping of human dynamin-1-like GTPase domain based on X-ray structure analyses. PLoS ONE 8, e71835 (2013).
Hermann, G. J. et al. Mitochondrial fusion in yeast requires the transmembrane GTPase Fzo1p. J. Cell. Biol. 143, 359–373 (1998).
Segall, D. E., Nelson, P. C. & Phillips, R. Volume-exclusion effects in tethered-particle experiments: bead size matters. Phys. Rev. Lett. 96, 088306 (2006).
Gasper, R., Meyer, S., Gotthardt, K., Sirajuddin, M. & Wittinghofer, A. It takes two to tango: regulation of G proteins by dimerization. Nat. Rev. Mol. Cell. Biol. 10, 423–429 (2009).
Orso, G. et al. Homotypic fusion of ER membranes requires the dynamin-like GTPase atlastin. Nature 460, 978–983 (2009).
Genevaux, P., Georgopoulos, C. & Kelley, W. L. The Hsp70 chaperone machines of Escherichia coli: a paradigm for the repartition of chaperone functions. Mol. Microbiol. 66, 840–857 (2007).
Toyofuku, M. et al. Prophage-triggered membrane vesicle formation through peptidoglycan damage in Bacillus subtilis. Nat. Commun. 8, 481–491 (2017).
Luthy, L., Grutter, M. G. & Mittl, P. R. E. The crystal structure of helicobacter cysteine-rich protein C at 2.0 angstrom resolution: Similar peptide-binding sites in TPR and SEL1-like repeat proteins. J. Mol. Biol. 340, 829–841 (2004).
Bramkamp, M. Structure and function of bacterial dynamin-like proteins. Biol. Chem. 393, 1203–1214 (2012).
Yan, L. et al. Structural basis for GTP hydrolysis and conformational change of MFN1 in mediating membrane fusion. Nat. Struct. Mol. Biol. 25, 233–243 (2018).
Chappie, J. S. et al. A pseudoatomic model of the dynamin polymer identifies a hydrolysis-dependent powerstroke. Cell 147, 209–222 (2011).
Gibson, D. G. et al. Enzymatic assembly of DNA molecules up to several hundred kilobases. Nat. Methods 6, 343–345 (2009).
Kabsch, W. Xds. Acta Crystallogr. D Biol. Crystallogr. 66, 125–132 (2010).
Evans, P. R. & Murshudov, G. N. How good are my data and what is the resolution? Acta Crystallogr. D Biol. Crystallogr. 69, 1204–1214 (2013).
Foadi, J. et al. Clustering procedures for the optimal selection of data sets from multiple crystals in macromolecular crystallography. Acta Crystallogr. D Biol. Crystallogr. 69, 1617–1632 (2013).
Adams, P. D. et al. PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr. D Biol. Crystallogr. 66, (213–221 (2010).
Emsley, P., Lohkamp, B., Scott, W. G. & Cowtan, K. Features and development of Coot. Acta Crystallogr. D Biol. Crystallogr. 66, 486–501 (2010).
Nicholls, R. A., Long, F. & Murshudov, G. N. Low-resolution refinement tools in REFMAC5. Acta Crystallogr. D Biol. Crystallogr. 68, 404–417 (2012).
DiMaio, F. et al. Improved low-resolution crystallographic refinement with Phenix and Rosetta. Nat. Methods 10, 1102–1104 (2013).
Liu, T. Y. et al. Cis and trans interactions between atlastin molecules during membrane fusion. Proc. Natl Acad. Sci. USA 112, E1851–E1860 (2015).
Beeby, M. et al. Diverse high-torque bacterial flagellar motors assemble wider stator rings using a conserved protein scaffold. Proc. Natl Acad. Sci. USA 113, E1917–E1926 (2016).
Bingham-Ramos, L. K. & Hendrixson, D. R. Characterization of two putative cytochrome c peroxidases of Campylobacter jejuni involved in promoting commensal colonization of poultry. Infect. Immun. 76, 1105–1114 (2008).
Noel, J. K., Whitford, P. C. & Onuchic, J. N. The shadow map: a general contact definition for capturing the dynamics of biomolecular folding and function. J. Phys. Chem. B 116, 8692–8702 (2012).
Onuchic, J. N. & Wolynes, P. G. Theory of protein folding. Curr. Opin. Struc. Biol. 14, 70–75 (2004).
Noel, J. K. et al. SMOG 2: a versatile software package for generating structure-based models. PLoS Comp. Biol. 12, e1004794 (2016).
Lammert, H., Schug, A. & Onuchic, J. N. Robustness and generalization of structure-based models for protein folding and function. Proteins-Struct. Funct. Bioinform. 77, 881–891 (2009).
We thank the beamline staff at Diamond synchrotron. Tillmann Pape and Marc Morgan for facility support. We acknowledge the gift of Campylobacter antibodies from David Hendrixson. Morgan Beeby, Bonnie Chaban, Brendan Wren and Ozan Gundogdu gave Campylobacter materials and expertise. Jan Löwe and Frank Bürmann gave manuscript feedback. This work was supported by a Wellcome Trust Fellowship (097328/Z/11/Z) to H.L.
The authors declare no competing interests.
Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Liu, J., Noel, J.K. & Low, H.H. Structural basis for membrane tethering by a bacterial dynamin-like pair. Nat Commun 9, 3345 (2018). https://doi.org/10.1038/s41467-018-05523-8
Phosphoinositide-binding proteins mark, shape and functionally modulate highly-diverged endocytic compartments in the parasitic protist Giardia lamblia
PLOS Pathogens (2020)
A Molecular Perspective on Mitochondrial Membrane Fusion: From the Key Players to Oligomerization and Tethering of Mitofusin
The Journal of Membrane Biology (2019)
Nature Communications (2019)
Nature Communications (2019)
The FASEB Journal (2019)