From brain to the World Wide Web, information-processing networks share common scale invariant properties. Here, we reveal the existence of neural-like networks at a molecular scale within the ribosome. We show that with their extensions, ribosomal proteins form complex assortative interaction networks through which they communicate through tiny interfaces. The analysis of the crystal structures of 50S eubacterial particles reveals that most of these interfaces involve key phylogenetically conserved residues. The systematic observation of interactions between basic and aromatic amino acids at the interfaces and along the extension provides new structural insights that may contribute to decipher the molecular mechanisms of signal transmission within or between the ribosomal proteins. Similar to neurons interacting through “molecular synapses”, ribosomal proteins form a network that suggest an analogy with a simple molecular brain in which the “sensory-proteins” innervate the functional ribosomal sites, while the “inter-proteins” interconnect them into circuits suitable to process the information flow that circulates during protein synthesis. It is likely that these circuits have evolved to coordinate both the complex macromolecular motions and the binding of the multiple factors during translation. This opens new perspectives on nanoscale information transfer and processing.
Ribosomes are large ribonucleoprotein particles that catalyse the mRNA-directed protein synthesis1. One of the most surprising features of ribosome structures was the finding that ribosomal proteins possess long filamentous and irregular extensions that penetrate deeply into the RNA core2,3,4. These extensions display features of intrinsically disordered proteins5 and have been thought to play a role in inter-protein communication6,7 or in ribosome assembly8,9,10. However, the molecular mechanisms underlying these putative functions are still poorly understood. The finding of two folding states in the crystal structure of the ribosomal protein bL2011 provided structural insights into the mechanism of signal transmission along an α-helical extension and stimulated us to search if similar properties are also observed in other ribosomal proteins. Here, a large-scale analysis of the ribosome particle structures of the three domains of life shows that an essential extension function is to connect distant ribosomal proteins.
Results and Discussion
The extensions that are observed in most of the ribosomal proteins systematically participate in networks with a great diversity of protein-protein interactions (Fig. 1, Table 1; Supplementary Tables S1–S7 and Figs S1–S3). Reciprocally, we show that the proteins that are not involved in protein-protein interactions are devoid of extensions. Also, from archaea to eukaryotes the number of inter-protein contacts greatly increases with the extension sizes and the number of extensions per protein (Table 1). The eukaryotic ribosome displays the highest number and diversity of inter-protein contacts. For a total of 80 protein-protein interactions in the 60S ribosomal subunit of eukaryotes, 62 are mediated through extensions that connect either the other extensions or the globular domains of their partners. Also, all the proteins of the 40S eukaryotic subunit and most of the bacterial and archaeal extensions participate in inter-protein contacts. All kinds of possible contacts between the different categories of extensions are observed in the three domains (Table 1, Figs 2 and 3). Direct contacts between globular domains are far less frequent than those involving extensions, thus supporting the hypothesis that extensions have evolved to connect proteins that are too distant to interact directly by their globular domains.
Secondly, our analysis shows that these networks present an interesting similarity with information processing networks (Figs 2 and 3; Supplementary Tables S8–S10 and Fig. S4). In the three domains, the proteins form scale-free and assortative networks containing highly connected hubs12. Eukaryotic 60S proteins form a single network, with most of the proteins connected to 3 or 4 partners. Through their multiple extensions, hubs such as eL15 and uL4 connect 7 and 8 partners that also belong to the most connected proteins (Fig. 2a; Supplementary Table S8). Similarly, uS8 interacts with 8 highly connected partners within the 40S subunit (Fig. 2b). Although less inter-connected, the bacterial and archaeal proteins also form assortative networks. For example, the eubacterial hubs uL3 and bL20 that are essential for 50S assembly interact with the most connected proteins (Fig. 3a; Supplementary Fig. S4). Another property of these networks is that they relate proteins whose globular domains are located on opposite sides of the subunits with only a few inter-node links. In addition, we observe network-motifs well known to participate in information processing, such as the feed-forward loops in the eukaryotic subunits (Supplementary Tables S9 and S10)13. Interestingly, as indicated by the number of inter-protein contacts/rRNA size ratio that is significantly higher in eukarya (Table 1), the ribosomal network connectivity is not simply proportional to the rRNA size but seems rather to reflect the growing ribosome complexity during evolution.
Thirdly, to decipher the underlying molecular mechanisms of information transmission within these networks, all the inter-protein contacts of the eubacterial large subunit have been systematically analysed. This network indeed provides the opportunity to compare and analyse the highest number of equivalent structures from three eubacterial species (E. coli, D. radiodurans and T. thermophilus) crystallized in different functional translation steps, initiation, elongation and termination with various factors and antibiotics1 (Supplementary Table S11). Most of the interface contact areas are unusually small, with values well below those classically expected for forming stable protein interactions14 (Table 2, Fig. 4). These interfaces are so minute, that they seem to have been systematically overlooked in previous studies. However, our analysis shows that they are phylogenetically and structurally well conserved, suggesting that they are likely to play an essential function. Indeed, sequence alignments provided by Y. Wolf15 indicate that, except in a few cases (uL16-bL25 and bL9-bL28), most of the interfaces contain highly conserved key amino acids, mainly aromatic and basic that establish specific intermolecular interactions in all the eubacterial species (Figs 5 and 6; Supplementary Table S12 and Fig. S5). All the recorded miniature inter-protein contacts have been systematically observed in the 50S structures of the three analysed species. Their comparison within all the available 50S and 70S structures whose resolution is higher than 3.5 Å shows that each interface exhibits a unique structure whatever the species or the translation steps in which the ribosomes have been crystallized (Supplementary Table S11). A notable exception is the uL16-bL27 pair that becomes fully ordered when the P-tRNA site is occupied by the P-tRNA (See Methods).
Remarkably, except uL16-bL27, all 50S protein-protein interfaces, from the smallest (3 aas, 25 Å2) to the largest (48 aas, 1709 Å2), contain conserved residues that are systematically involved in one and most frequently several intra- or inter-molecular basic-aromatic amino acid interactions16 (Table 2, Figs 5 and 6). In addition, in more than half of them, these cation-π interactions have been found in close vicinity to salt-bridges. Thus, the interfaces are split in two main groups: (i) cation-π, and (ii) the cation-π/salt-bridge groups. In a few cases such as uL15-uL4, uL23-uL29 and uL3-bL19, proline-aromatic amino acid interactions are also observed17 (Table 2). The largest interfaces (from 400 to 1700 Å2) are further stabilised by additional intermolecular contacts such as hydrophobic interactions and hydrogen bonds that are usually observed in classical dimers. The major finding of this analysis is that the smallest interfaces display a “necessary minimum” that is also shared by larger ones: the conserved aromatic-basic amino acid interactions. Too tiny to be rationalized in terms of dimer stabilisation, these highly conserved interfaces have probably been selected during evolution to play a specific role in inter-protein communication. They reveal the strictly necessary interacting residues to ensure information transfer from a protein to another. Indeed, it has been experimentally shown that cation-π interactions mediate inter-domain communication in proteins18, and participate in information transfer in the central nervous system by mediating the interactions between the neurotransmitters and their receptors16. Particularly interesting is the observation that these basic-aromatic amino acid interactions also spread without interruption along the extensions and form a regularly distributed array of intra-molecular interactions along the whole protein network (Fig. 7a). RNA bases have been also found to substitute the aromatic residues when they are lacking, to ensure continuity in the interaction network, as found for example within the bL17-uL3 connecting segment (Fig. 7b).
The ribosomal wires are reminiscent of DNA19 or bacterial nanowires20 known to perform metal-like charge transfer through the π-orbitals of the DNA bases or the periodic arrays of aromatic residues. It would be interesting to test if ribosomal wires are able to transmit an electric signal, by linking distant proteins of the network within an intact ribosome, to the luminescent probes developed to monitor charge transport along DNA19. Alternatively, the ribosomal wires may use a still unknown mechanism for signal transduction that involves an array of contiguous cation-π interactions. One could imagine that electrostatic perturbations induced by the binding of tRNAs or translation factors could be propagated as a wave along the wire.
Viewing ribosomal protein extensions as connecting wires that play a role in information transfer is consistent with experimental data showing that RNA21,22 and some proteins23,24,25 participate in allosteric coordination and information exchange between distant parts of the ribosome. In addition, our study provides new structural insights to decipher the molecular mechanisms of allosteric communication within disordered proteins26,27. Since the extensions and interfaces of the small and large ribosomal subunits of the three cellular domains have similar sequence and structural features, it is likely that they all share the property of forming cross-talk networks. Eubacterial ribosomal communication pathways such as the uL13-uL3 interface are indeed universally conserved across the three domains of life, while others are replaced by convergence in archaea and eukaryota (Supplementary Figs S6–S9). Particular triplet motifs are also recurrently observed in the three domain’s ribosomes, implying they might play a specific function.
It could be asked why highly interconnected ribosomal protein networks have evolved with a growing complexity during evolution, since RNA can also ensure allosteric communication. During translation, ribosomes orchestrate the binding of mRNA, tRNAs and multiple translation factors28. Each of the three main translation stages (initiation, elongation and termination) requires the sequential binding and release of specific translation factors. During the elongation cycle the ribosomes coordinate complex movements such as the coupled translocation of tRNAs and mRNA that are associated with large-scale structural rearrangements29. The peptide bond formation and the extrusion of the nascent peptide through the exit tunnel must be also coordinated with the tRNA and mRNA translocation. In addition, in order to coordinate cellular responses to environmental changes, the ribosome activity is regulated by factors that adapt translation to cell activity. The recent structure of BipA, a GTPase involved in bacterial stress response, bound to the ribosome in its active state has provided new insights about these processes30.
It is likely that this complex molecular machine should require a system of information transfer and processing to coordinate its multiple tasks and sequential movements. From a functional point of view, our study shows that the 50S protein network is indeed organized along the path of tRNA translocation and around the peptide exit tunnel (Fig. 7c,d). Similar to an organisation into sensory- and inter-neurons connections in simple brains31, the sensory-ribosomal proteins uL16, bL27, uL5, bL33 literally “innervate” the three key A, P and E-tRNA sites while uL4, uL22 and uL23 sense the interior of the peptide exit tunnel32 through their extensions. It has been shown that the uL16-bL27 interface may behave as an electrostatic sensor that becomes fully ordered when the P-tRNA is bound. On the other hand, inter-neuron-like proteins interconnect proteins that sense distant functional sites. Ribosomal proteins therefore display at a nano-scale the characteristics of “molecular neurons” interacting together through “molecular synapses”. This neural-like organisation strongly suggests that the network has the property to not only transfer but also process the information coming from distant functional ribosomal sites. In a preliminary model, we propose the 50S protein network processes the information flow that circulates between the tRNA binding sites and peptide tunnel to coordinate the complex tasks and motions during protein synthesis (Fig. 7d). One could speculate that information processing ability is restricted to protein circuits, thus explaining why they have evolved to complement allosteric “transfer only” rRNA networks. The ribosomal protein networks perhaps constitute some of the most striking examples of “proteins as computing element in the cell” as formulated by D. Bray, twenty years ago33.
All the structures of eukaryotic, eubacterial and archaeal ribosomes deposited in the protein data bank (PDB)34 have been systematically analysed in order to characterize their extensions and their inter-proteins contacts. The nomenclature of ribosomal proteins used in the tables and figures follows the a new system for naming ribosomal proteins that has been recently adopted35 (see also the site of N. Ban laboratory: http://www.bangroup.ethz.ch/research/nomenclature-of-ribosomal-proteins.html). The tables for the conversion between the old and the new system are provided in Supplementary Tables S13 and S14. The extensions have been defined as elongated protein chains protruding from the globular domain. Segments (seg) are extensions from the N-terminus or the C-terminus ends devoid of secondary structure, mixed extensions (mix) combine helical (H) and unstructured chains (S). Structured extensions contain α-helices (H), loops (L) or β-hairpins (B). Interactions between extensions or between extensions and globular domain have been systematically detected with the program pymol36 when inter-molecular distances are less or equal to 4 Å.
Scripts have been written for systematically mapping the protein-protein interactions within the ribosomal subunit for display by the program circos37. The ribosomal protein networks of the large and small subunits of the three domains have been characterized according to the parameters defined in Barabasi et al.12. Network motifs detection in non-directed networks has been performed with the program mfinder provided by U. Alon13.
Sequence alignments, interface characterization and structural analysis
The sequence alignments of all the eubacterial ribosomal proteins have been kindly provided by U. Wolf and N. Yutin15. They can be downloaded from the site: ftp://ftp.ncbi.nih.gov/pub/wolf/_suppl/ribo. The aligned sequences have been visualized and analysed with the program Jalview38. Consensus sequences and conserved residues of the ribosomal proteins at the interface area have been represented in Supplementary Fig. S5, with the “zappo” colouring scheme and in Supplementary Table S12. Conserved residues have been integrated in pymol scripts for their three-dimensional representation and zappo colouring (Figs 5 and 6).
Structural analysis of the interfaces
The structures of each interacting protein pairs have been analysed in all the available PDB crystallographic structures of three species (T. thermophilus, D. radiodurans and E. coli) 50S and 70S subunits whose resolution is greater than 3.5 Å (Supplementary Table S11). Pymol scripts have been developed to systematically superimpose together all the equivalent protein models in order to compare them at the interface regions. Although homologous 50S proteins superimpose extremely well, twelve interfaces have been found to differ from one structure to the next (Supplementary Table S15 and Fig. S10). Knowing that in the resolution range (2.9–3.5 Å) misinterpretation of electron density maps in unclear regions are possible, we have carefully checked the reliability of these different models by the systematic analysis of their electron density maps. The program Phenix39 has been automated to compute 2fo-fc and difference maps of all the models listed in Supplementary Tables S11 and S15, from their structure factors deposited into the PDB. Pymol scripts have been developed to systematically compare the maps at the sites where structural difference have been observed. Based on the high quality of electron density maps of recent high resolution structures (4v8i, 4y4o, 4ybb, 4z8c, 4w2h, 4w2f, 4y4p) and the careful comparison of the density maps, our analysis has revealed that in most cases, the conformation “x” (coloured in red in Supplementary Table S15 and reported Supplementary Fig. S10) corresponds to misinterpretations of poorly resolved maps in these regions (Supplementary Fig. S11). For example, our analysis reveals that the residues built in the alternative conformation “x” have been in fact, fitted into density peaks corresponding to neighbouring residues (see legend of Supplementary Fig. S11). We deduced that the all the of the 50S subunit interfaces display a unique conformation whatever the species, the crystallization conditions, the translation factor and antibiotic added or the translation step in which the ribosome has been crystallized. The protein interfaces are both phylogenetically and structurally extremely well conserved. Consequently, we have focused our structural analysis on reliable high-resolution structures (T. thermophilus: 4v8i, 4w2f, 4w2h, 4z8c, 4y4o, 4y4p; E. coli: 4ybb and D. radiodurans: 5dm6).
The protein pair interfaces extracted from these models have been characterized with areaimol from the CCP4 program suite40. The analysis of intermolecular interactions at the interfaces has been performed by visual inspection of the interface structures and by using the web server PIC41. Ribosomal subunits of archaea, eubacteria and eukaryota have been also systematically superimposed in order to compare their networks and connections. All the scripts that have been developed in this study can be sent by mail on demand.
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We thank P. Hingamp, O. Hyrien, M. Lescot-David, M. Springer and E. Westhof for helpful discussions and critical reading of the manuscript. We are grateful to S. Santini for helpful discussions and F. Jean for his help in network characterisation.
The authors declare no competing financial interests.
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Poirot, O., Timsit, Y. Neuron-Like Networks Between Ribosomal Proteins Within the Ribosome. Sci Rep 6, 26485 (2016). https://doi.org/10.1038/srep26485
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