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The ABC exporter IrtAB imports and reduces mycobacterial siderophores


Intracellular replication of the deadly pathogen Mycobacterium tuberculosis relies on the production of small organic molecules called siderophores that scavenge iron from host proteins1. M. tuberculosis produces two classes of siderophore, lipid-bound mycobactin and water-soluble carboxymycobactin2,3. Functional studies have revealed that iron-loaded carboxymycobactin is imported into the cytoplasm by the ATP binding cassette (ABC) transporter IrtAB4, which features an additional cytoplasmic siderophore interaction domain5. However, the predicted ABC exporter fold of IrtAB is seemingly contradictory to its import function. Here we show that membrane-reconstituted IrtAB is sufficient to import mycobactins, which are then reduced by the siderophore interaction domain to facilitate iron release. Structure determination by X-ray crystallography and cryo-electron microscopy not only confirms that IrtAB has an ABC exporter fold, but also reveals structural peculiarities at the transmembrane region of IrtAB that result in a partially collapsed inward-facing substrate-binding cavity. The siderophore interaction domain is positioned in close proximity to the inner membrane leaflet, enabling the reduction of membrane-inserted mycobactin. Enzymatic ATPase activity and in vivo growth assays show that IrtAB has a preference for mycobactin over carboxymycobactin as its substrate. Our study provides insights into an unusual ABC exporter that evolved as highly specialized siderophore-import machinery in mycobacteria.

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Fig. 1: Structure of IrtAB.
Fig. 2: Biochemical characterization of IrtAB.
Fig. 3: In vivo characterization of IrtAB in M. smegmatis.
Fig. 4: Proposed mechanism of IrtAB-mediated mycobactin uptake.

Data availability

The crystal structures of the SID and IrtAB-Syb_NL5 have been deposited in the Protein Data Bank (PDB) under entries 6TEK and 6TEJ, respectively The cryo-EM map has been deposited in the Electron Microscopy Data Bank under accession number EMD-10319. Plasmids, strains, the sybody Syb_NL5 and raw data are available from the authors upon reasonable request.


  1. 1.

    De Voss, J. J. et al. The salicylate-derived mycobactin siderophores of Mycobacterium tuberculosis are essential for growth in macrophages. Proc. Natl Acad. Sci. USA 97, 1252–1257 (2000).

    ADS  PubMed  Google Scholar 

  2. 2.

    Snow, G. A. & White, A. J. Chemical and biological properties of mycobactins isolated from various mycobacteria. Biochem. J. 115, 1031–1045 (1969).

    CAS  PubMed  PubMed Central  Google Scholar 

  3. 3.

    Gobin, J. et al. Iron acquisition by Mycobacterium tuberculosis: isolation and characterization of a family of iron-binding exochelins. Proc. Natl Acad. Sci. USA 92, 5189–5193 (1995).

    ADS  CAS  PubMed  Google Scholar 

  4. 4.

    Rodriguez, G. M. & Smith, I. Identification of an ABC transporter required for iron acquisition and virulence in Mycobacterium tuberculosis. J. Bacteriol. 188, 424–430 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Ryndak, M. B., Wang, S., Smith, I. & Rodriguez, G. M. The Mycobacterium tuberculosis high-affinity iron importer, IrtA, contains an FAD-binding domain. J. Bacteriol. 192, 861–869 (2010).

    CAS  PubMed  Google Scholar 

  6. 6.

    Wells, R. M. et al. Discovery of a siderophore export system essential for virulence of Mycobacterium tuberculosis. PLoS Pathog. 9, e1003120 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  7. 7.

    Siegrist, M. S. et al. Mycobacterial Esx-3 is required for mycobactin-mediated iron acquisition. Proc. Natl Acad. Sci. USA 106, 18792–18797 (2009).

    ADS  PubMed  Google Scholar 

  8. 8.

    Tufariello, J. M. et al. Separable roles for Mycobacterium tuberculosis ESX-3 effectors in iron acquisition and virulence. Proc. Natl Acad. Sci. USA 113, E348–E357 (2016).

    CAS  PubMed  Google Scholar 

  9. 9.

    Locher, K. P. Mechanistic diversity in ATP-binding cassette (ABC) transporters. Nat. Struct. Mol. Biol. 23, 487–493 (2016).

    CAS  PubMed  Google Scholar 

  10. 10.

    ter Beek, J., Guskov, A. & Slotboom, D. J. Structural diversity of ABC transporters. J. Gen. Physiol. 143, 419–435 (2014).

    PubMed  PubMed Central  Google Scholar 

  11. 11.

    Zimmermann, I. et al. Synthetic single domain antibodies for the conformational trapping of membrane proteins. eLife 7, e34317 (2018).

    PubMed  PubMed Central  Google Scholar 

  12. 12.

    Egloff, P. et al. Engineered peptide barcodes for in-depth analyses of binding protein libraries. Nat. Methods 16, 421–428 (2019).

    CAS  PubMed  Google Scholar 

  13. 13.

    Holm, L. & Laakso, L. M. Dali server update. Nucleic Acids Res. 44, W351–W355 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  14. 14.

    Hutter, C. A. J. et al. The extracellular gate shapes the energy profile of an ABC exporter. Nat. Commun. 10, 2260 (2019).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  15. 15.

    Hohl, M., Briand, C., Grütter, M. G. & Seeger, M. A. Crystal structure of a heterodimeric ABC transporter in its inward-facing conformation. Nat. Struct. Mol. Biol. 19, 395–402 (2012).

    CAS  PubMed  Google Scholar 

  16. 16.

    Miethke, M., Hou, J. & Marahiel, M. A. The siderophore-interacting protein YqjH acts as a ferric reductase in different iron assimilation pathways of Escherichia coli. Biochemistry 50, 10951–10964 (2011).

    CAS  PubMed  Google Scholar 

  17. 17.

    Hürlimann, L. M. et al. The heterodimeric ABC transporter EfrCD mediates multidrug efflux in Enterococcus faecalis. Antimicrob. Agents Chemother. 60, 5400–5411 (2016).

    PubMed  PubMed Central  Google Scholar 

  18. 18.

    Ambudkar, S. V. et al. Partial purification and reconstitution of the human multidrug-resistance pump: characterization of the drug-stimulatable ATP hydrolysis. Proc. Natl Acad. Sci. USA 89, 8472–8476 (1992).

    ADS  CAS  PubMed  Google Scholar 

  19. 19.

    Lee, J. Y., Yang, J. G., Zhitnitsky, D., Lewinson, O. & Rees, D. C. Structural basis for heavy metal detoxification by an Atm1-type ABC exporter. Science 343, 1133–1136 (2014).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Tombline, G., Bartholomew, L. A., Urbatsch, I. L. & Senior, A. E. Combined mutation of catalytic glutamate residues in the two nucleotide binding domains of P-glycoprotein generates a conformation that binds ATP and ADP tightly. J. Biol. Chem. 279, 31212–31220 (2004).

    CAS  PubMed  Google Scholar 

  21. 21.

    Al-Shawi, M. K., Polar, M. K., Omote, H. & Figler, R. A. Transition state analysis of the coupling of drug transport to ATP hydrolysis by P-glycoprotein. J. Biol. Chem. 278, 52629–52640 (2003).

    CAS  PubMed  Google Scholar 

  22. 22.

    Geertsma, E. R., Nik Mahmood, N. A., Schuurman-Wolters, G. K. & Poolman, B. Membrane reconstitution of ABC transporters and assays of translocator function. Nat. Protoc. 3, 256–266 (2008).

    CAS  PubMed  Google Scholar 

  23. 23.

    Dragset, M. S. et al. Genome-wide phenotypic profiling identifies and categorizes genes required for mycobacterial low iron fitness. Sci. Rep. 9, 11394 (2019).

    ADS  PubMed  PubMed Central  Google Scholar 

  24. 24.

    Arnold, F. M. et al. A uniform cloning platform for mycobacterial genetics and protein production. Sci. Rep. 8, 9539 (2018).

    ADS  PubMed  PubMed Central  Google Scholar 

  25. 25.

    Prados-Rosales, R. et al. Role for Mycobacterium tuberculosis membrane vesicles in iron acquisition. J. Bacteriol. 196, 1250–1256 (2014).

    PubMed  PubMed Central  Google Scholar 

  26. 26.

    Quazi, F., Lenevich, S. & Molday, R. S. ABCA4 is an N-retinylidene-phosphatidylethanolamine and phosphatidylethanolamine importer. Nat. Commun. 3, 925 (2012).

    ADS  PubMed  PubMed Central  Google Scholar 

  27. 27.

    Xu, D. et al. Cryo-EM structure of human lysosomal cobalamin exporter ABCD4. Cell Res. 29, 1039–1041 (2019).

    PubMed  Google Scholar 

  28. 28.

    Santelia, D. et al. MDR-like ABC transporter AtPGP4 is involved in auxin-mediated lateral root and root hair development. FEBS Lett. 579, 5399–5406 (2005).

    CAS  PubMed  Google Scholar 

  29. 29.

    Perez, C. et al. Structure and mechanism of an active lipid-linked oligosaccharide flippase. Nature 524, 433–438 (2015).

    ADS  CAS  PubMed  Google Scholar 

  30. 30.

    Ratledge, C. & Ewing, M. The occurrence of carboxymycobactin, the siderophore of pathogenic mycobacteria, as a second extracellular siderophore in Mycobacterium smegmatis. Microbiology 142, 2207–2212 (1996).

    CAS  PubMed  Google Scholar 

  31. 31.

    Geertsma, E. R. & Dutzler, R. A versatile and efficient high-throughput cloning tool for structural biology. Biochemistry 50, 3272–3278 (2011).

    CAS  PubMed  Google Scholar 

  32. 32.

    Mastronarde, D. N. Automated electron microscope tomography using robust prediction of specimen movements. J. Struct. Biol. 152, 36–51 (2005).

    PubMed  PubMed Central  Google Scholar 

  33. 33.

    Scheres, S. H. RELION: implementation of a Bayesian approach to cryo-EM structure determination. J. Struct. Biol. 180, 519–530 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  34. 34.

    Zivanov, J. et al. New tools for automated high-resolution cryo-EM structure determination in RELION-3. eLife 7, e42166 (2018).

    PubMed  PubMed Central  Google Scholar 

  35. 35.

    Zheng, S. Q. et al. MotionCor2: anisotropic correction of beam-induced motion for improved cryo-electron microscopy. Nat. Methods 14, 331–332 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  36. 36.

    Rohou, A. & Grigorieff, N. CTFFIND4: fast and accurate defocus estimation from electron micrographs. J. Struct. Biol. 192, 216–221 (2015).

    PubMed  PubMed Central  Google Scholar 

  37. 37.

    Moeller, A. et al. Distinct conformational spectrum of homologous multidrug ABC transporters. Structure 23, 450–460 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  38. 38.

    Chen, S. et al. High-resolution noise substitution to measure overfitting and validate resolution in 3D structure determination by single particle electron cryomicroscopy. Ultramicroscopy 135, 24–35 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  39. 39.

    Rosenthal, P. B. & Henderson, R. Optimal determination of particle orientation, absolute hand, and contrast loss in single-particle electron cryomicroscopy. J. Mol. Biol. 333, 721–745 (2003).

    CAS  PubMed  Google Scholar 

  40. 40.

    Scheres, S. H. W. & Chen, S. Prevention of overfitting in cryo-EM structure determination. Nat. Methods 9, 853–854 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  41. 41.

    Heymann, J. B. & Belnap, D. M. Bsoft: image processing and molecular modeling for electron microscopy. J. Struct. Biol. 157, 3–18 (2007).

    CAS  Google Scholar 

  42. 42.

    Cardone, G., Heymann, J. B. & Steven, A. C. One number does not fit all: mapping local variations in resolution in cryo-EM reconstructions. J. Struct. Biol. 184, 226–236 (2013).

    PubMed  Google Scholar 

  43. 43.

    Tan, Y. Z. et al. Addressing preferred specimen orientation in single-particle cryo-EM through tilting. Nat Methods 14, 793–796 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  44. 44.

    Kabsch, W. XDS. Acta Crystallogr. D 66, 125–132 (2010).

    CAS  PubMed  Google Scholar 

  45. 45.

    McCoy, A. J. et al. Phaser crystallographic software. J. Appl. Crystallogr. 40, 658–674 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  46. 46.

    Emsley, P. & Cowtan, K. Coot: model-building tools for molecular graphics. Acta Crystallogr. D 60, 2126–2132 (2004).

    PubMed  Google Scholar 

  47. 47.

    Adams, P. D. et al. PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr. D 66, 213–221 (2010).

    CAS  PubMed  Google Scholar 

  48. 48.

    Pettersen, E. F. et al. UCSF Chimera—a visualization system for exploratory research and analysis. J. Comput. Chem. 25, 1605–1612 (2004).

    CAS  PubMed  Google Scholar 

  49. 49.

    Voss, N. R. & Gerstein, M. 3V: cavity, channel and cleft volume calculator and extractor. Nucleic Acids Res. 38, W555–W562 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  50. 50.

    Bukowska, M. A. et al. A transporter motor taken apart: flexibility in the nucleotide binding domains of a heterodimeric ABC exporter. Biochemistry 54, 3086–3099 (2015).

    CAS  PubMed  Google Scholar 

  51. 51.

    Hohl, M. et al. Increased drug permeability of a stiffened mycobacterial outer membrane in cells lacking MFS transporter Rv1410 and lipoprotein LprG. Mol. Microbiol. 111, 1263–1282 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  52. 52.

    Hohl, M. et al. Structural basis for allosteric cross-talk between the asymmetric nucleotide binding sites of a heterodimeric ABC exporter. Proc. Natl Acad. Sci. USA 111, 11025–11030 (2014).

    ADS  CAS  PubMed  Google Scholar 

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We thank all members of the Seeger laboratory for discussions; B. Blattmann, C. Stutz-Ducommun and S. Eberle of the Protein Crystallization Center UZH for performing the crystallization screening; the staff of the SLS beamlines X06SA and X06DA for their support during data collection; and J. Sobeck of the Functional Genomics Center Zurich for support during SPR measurements. We also thank all members of the Medalia laboratory, especially M. Eibauer, for discussions and the Center for microscopy and image analysis (ZMB) of the UZH for providing help and equipment. Work in the laboratory of M.A.S. was supported by the European Research Council (ERC) (consolidator grant no. 772190), a SNSF Professorship of the Swiss National Science Foundation (PP00P3_144823) and a grant of the Novartis Foundation for Medical-Biological Research. Work in the laboratory of O.M. was supported by the Swiss National Science Foundation (grant 31003A_179418) and the Mäxi Foundation. Work in the laboratory of G.M. was supported by the Robert A. Welch Foundation (grant no. AT-1935-20170325) and by the National Institute of General Medical Sciences of the National Institutes of Health (R35GM128704). F.M.A., M.S.W. and I.G. were supported by three Candoc fellowships of the University of Zurich.

Author information




F.M.A. and M.A.S. conceived the project. F.M.A. cloned all ORFs, established the protein purification protocols, and generated gene deletions in M. smegmatis. F.M.A. established the mycobactin extraction protocols with the help of S.A. and carried out the majority of the biochemical and in vivo characterization of IrtAB. F.M.A., I.G. and L.M.H. carried out 55Fe-cMBT transport assays with intact cells and proteoliposomes. F.M.A. selected Syb_NL5 with the help of P.E. and I.Z. M.S.W. carried out all cryo-EM work and data analysis under the supervision of O.M. with samples prepared by F.M.A. F.M.A. solved the structure of the SID with the support of C.A.J.H. I.G. crystallized the IrtAB-Syb_NL5 complex with the help of F.M.A. and solved its structure with the help of M.A.S. I.G. built the IrtAB model with the support of C.A.J.H. and M.A.S. M.J.G. carried out the mycobactin reduction experiments under the supervision of G.M. E.E.P. purified mycobactins by HPLC under the supervision of J.P. F.M.A., M.S.W., I.G., G.M., O.M. and M.A.S. interpreted the data. F.M.A., M.S.W., I.G. and M.A.S. prepared figures, F.M.A., M.S.W. and M.A.S. wrote the paper, and I.G., G.M. and O.M. edited the paper.

Corresponding author

Correspondence to Markus A. Seeger.

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The authors declare no competing interests.

Additional information

Peer review information Nature thanks Gregory Cook, Damian Ekiert, Georgia Isom and Jochen Zimmer for their contribution to the peer review of this work.

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Extended data figures and tables

Extended Data Fig. 1 Sequence identity of IrtAB homologues and crystal structure of IrtAB determined with the aid of a sybody.

a, Sequence identity matrix of full-length IrtAB from M. thermoresistibile (Mth), M. smegmatis (Msm) and M. tuberculosis (Mtb). b, IrtAB(ΔSID) of M. thermoresistibile (lacking the SID and the linker between the SID and the TMD of IrtA) was crystallized with the aid of a sybody. IrtA is coloured in turquoise, IrtB in purple and the sybody in grey with CDR1, CDR2 and CDR3 coloured in yellow, orange and red, respectively. CDR, complementary determining region.

Extended Data Fig. 2 Cryo-EM data processing of IrtAB.

a, Typical motion-corrected cryo-EM micrograph of the detergent-solubilized IrtAB sample. Scale bar, 50 nm. b, Representative 2D class averages used for 3D reconstruction, showing side and bottom views. c, The data-processing workflow. High-quality micrographs (2,168) were selected after motion correction and used for autopicking of 335,045 particles. Several rounds of 2D classification were performed to remove false positives, yielding 167,781 IrtAB particles, which were subjected to 3D classification. One out of six classes (indicated by the black box), containing 70,257 particles, revealed distinct structural features of IrtAB with its SID and was subjected to 3D refinement. The resulting structure was used to subtract the detergent micelle from the raw particles. Afterwards, a focused 3D refinement without the detergent micelle was performed. The resulting map was sharpened using a B-factor of −319 Å2. The final structure was resolved to 6.88 Å and reveals details of the TMDs, the NBDs and the SID.

Extended Data Fig. 3 Cryo-EM data validation.

a, Angular distribution plot of all IrtAB particles that contributed to the final map. The map and the angular distribution plot have the same orientation. The height and colour (from blue to red) of the cylinder bars is proportional to the number of particles in those views. b, Plot of the directional FSC that represents a measure of directional resolution anisotropy. Shown are the global FSC (red line), the spread of directional resolution values defined by ±1 standard deviation from the mean of the directional resolutions (area encompassed by the green dotted lines) and a histogram of 100 directional resolutions evenly sampled over the 3D FSC (blue bars). A sphericity of 0.978 was determined at an FSC threshold of 0.5, which indicates very isotropic angular distribution (a value of 1 stands for completely isotropic angular distribution). The global resolution was determined to 6.9 Å (0.143 threshold). Directional FSC determination was performed with the 3DFSC software. c, FSC plot of the final density map of IrtAB. The plot shows the unmasked (green), masked (blue), phase randomized (red) and masking-effect-corrected (black) FSC curves. The resolution at which the gold-standard FSC curve drops below the 0.143 threshold is indicated. d, Local resolution variations in the cryo-EM map. The resolution ranges from 5.5 to 10.8 Å, as calculated by BlocRes.

Extended Data Fig. 4 Superimpositions with ABC exporter structures and structural comparison of IrtAB and TM287/288.

a, Superimposition of ABC exporters using the MatchMaker tool of Chimera. Nidelmann–Wunsch alignment algorithm and Blossom-62 matrix was used. r.m.s.d. (Å2) values were calculated over the entire polypeptide chains—that is, without pruning of long atom pairs. In the case that the asymmetric unit contained several polypeptides of identical sequence, chain A was taken for analysis (indicated as ‘A’ in the protein name). IF, inward-facing; OCC, occluded; OF, outward-facing. b, Structural deviations between IrtAB and the ABC exporter TM287/288 (PDB: 4Q4H). Shown is the structure of IrtAB in an ‘open-book representation’ with the entire transporter in the middle and the two half-transporters on the left (IrtB with domain-swap-helices TMH4 and TMH5 of IrtA) and on the right (IrtA with domain-swap-helices of IrtB). The structures are shown in sausage representation in which the thickness and colour gradient from blue to red indicate variable degrees of structural deviations between IrtAB and TM287/288. Major structural deviations in the TMDs of IrtB are indicated.

Extended Data Fig. 5 Full-length IrtAB structure shown in the membrane context.

MBT molecules with a C17 aliphatic chain length are shown in stick representation. The SID is orientated towards the membrane with its mycobactin binding pocket (yellow  ellipsoid) facing the inner leaflet. IrtAB is coloured as in Fig. 1.

Extended Data Fig. 6 ATPase activity measurements using HPLC-purified mycobactins of defined masses.

a, Reversed-phase chromatography separation by HPLC of Fe-cMBT (top) and Fe-MBT (bottom) isolated from M. smegmatis. Masses of mycobactins giving rise to the main peaks were determined by mass spectrometry. These analyses were performed once. b, Chemical structures of Fe-cMBT and Fe-MBT. c, ATPase activities of nanodisc-reconstituted IrtAB measured in the presence of Fe-cMBT or Fe-MBT of defined mass isolated by HPLC. Crude extracts of mycobactins were included as controls. Mycobactins were added at a concentration of 5 μM. Data points are technical triplicates, which were used to calculate the mean value (black bar). d, ATPase stimulation curves determined over a range of mycobactin concentrations for HPLC-purified samples of defined mass or the respective crude extracts. Data points are technical triplicates and curves cross through the mean values.

Extended Data Fig. 7 Mycobactin reduction by purified SID.

a, Reduction of Fe(iii)-MBT (100 μM) by M. thermoresistibile and M. smegmatis SIDs using NADPH as an electron donor and ferene as a reporter probe of released Fe(ii) (Amax = 590 nm). The 3×E mutant SID(3×E) served as a negative control. Representative data of biological duplicates are shown. b, Reduction of Fe(iii)-MBT by the SID of M. thermoresistibile performed at different concentrations of Fe(iii)-MBT. The data were fitted using the Michaelis–Menten equation. Data points are technical replicates.

Extended Data Fig. 8 Siderophore-dependent growth assay.

When grown in minimal medium (MM) under controlled iron concentrations, wild-type M. smegmatis, the M. smegmatis ΔfxbAΔmbtD double mutant (DKO) and the M. smegmatis ΔfxbAΔmbtDΔirtAB triple mutant (TKO) showed no significant differences in growth. Upon addition of the weak iron chelator 2,2′-dipyridyl, only the wild-type strain was able to grow owing to its ability to synthesize siderophores that extract iron bound to 2,2′-dipyridyl. Data points are technical triplicates and curves cross through the mean values.

Extended Data Table 1 Cryo-EM data collection and processing statistics
Extended Data Table 2 X-ray data collection and refinement statistics

Supplementary information

Supplementary Table 1

A list of primer sequences.

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Arnold, F.M., Weber, M.S., Gonda, I. et al. The ABC exporter IrtAB imports and reduces mycobacterial siderophores. Nature 580, 413–417 (2020).

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