Convergent evolution of small molecule pheromones in pristionchus nematodes

This is the final version. Available from eLife Sciences Publications via the DOI in this recordData availability: All data generated during this study are included in the manuscript and supporting files. Source data files have been provided.The small molecules that mediate chemical communication between nematodes—so-called “nematode-derived-modular-metabolites” (NDMMs)—are of major interest due to their ability to regulate development, behavior, and life-history. Pristionchus pacificus nematodes produce an impressive diversity of structurally complex NDMMs, some of which act as primer pheromones capable of triggering irreversible developmental switches. Many of these NDMMs have only ever been found in P. pacificus but no attempts had been made to study their evolution by profiling closely related species. This study was designed to bring a comparative perspective to the biochemical study of NDMMs via the systematic MS/MS and NMR-based analysis of exo-metabolomes from over 30 Pristionchus species. We identified 36 novel compounds and found evidence for the convergent evolution of complex NDMMs in separate branches of the Pristionchus phylogeny. Our results demonstrate that biochemical innovation is a recurrent process in Pristionchus nematodes, a pattern likely typical across the animal kingdom.Max Planck Societ

AbrB-like transcription factors assume a swapped hairpin fold that is evolutionarily related to double-psi beta barrels.

AbrB is a key transition-state regulator of Bacillus subtilis. Based on the conservation of a βαβ structural unit, we proposed a β barrel fold for its DNA binding domain, similar to, but topologically distinct from, double-psi β barrels. However, the NMR structure revealed a novel fold, the “looped-hinge helix.” To understand this discrepancy, we undertook a bioinformatics study of AbrB and its homologs; these form a large superfamily, which includes SpoVT, PrlF, MraZ, addiction module antidotes (PemI, MazE), plasmid maintenance proteins (VagC, VapB), and archaeal PhoU homologs. MazE and MraZ form swapped-hairpin β barrels. We therefore reexamined the fold of AbrB by NMR spectroscopy and found that it also forms a swapped-hairpin barrel. The conservation of the core βαβ element supports a common evolutionary origin for swapped-hairpin and double-psi barrels, which we group into a higher-order class, the cradle-loop barrels, based on the peculiar shape of their ligand binding site

Diagonal-free 3D/4D HN,HN-TROSY-NOESY-TROSY

Structural biology by NMR spectroscopy relies on measuring interproton distances via NOE cross-signals in nuclear Overhauser effect spectroscopy (NOESY) spectra. In proteins, the subset of H(N)-H'(N) NOE contacts is most important for deriving initial structural models and for spectral assignment by "NOE walking". Here we present a fully optimized NMR experiment for measuring these pivotal contacts: diagonal-free 3D/4D HN,HN-TROSY-NOESY-TROSY. It combines all of the critical requirements for extracting the optimal H(N)-H'(N) distance information: the highest resolution by consistent transverse relaxation-optimized spectroscopy (TROSY) evolution, the largest spectral dispersion in two (15)N dimensions, and maximal coverage and purity through specific suppression of the intense diagonal signals that are the main source of overlap, artifacts, and bias in any NOESY spectrum. Most notably, diagonal suppression here comes without compromising the NOE cross-signal intensities. This optimized experiment appears to be ideal for a broad range of structural studies, particularly on large deuterated, partially unfolded, helical, and membrane proteins

Mapping Local Conformational Landscapes of Proteins in Solution

The ability of proteins to adopt multiple conformational states is essential to their function, and elucidating the details of such diversity under physiological conditions has been a major challenge. Here we present a generalized method for mapping protein population landscapes by NMR spectroscopy. Experimental NOESY spectra are directly compared with a set of expectation spectra back-calculated across an arbitrary conformational space. Signal decomposition of the experimental spectrum then directly yields the relative populations of local conformational microstates. In this way, averaged descriptions of conformation can be eliminated. As the method quantitatively compares experimental and expectation spectra, it inherently delivers an R factor expressing how well structural models explain the input data. We demonstrate that our method extracts sufficient information from a single 3D NOESY experiment to perform initial model building, refinement, and validation, thus offering a complete de novo structure determination protocol

Optimized measurement temperature gives access to the solution structure of a 49 kDa homohexameric β-propeller

Ph1500 is a homohexameric, two-domain protein of unknown function from the hyperthermophilic archaeon Pyrococcus horikoshii. The C-terminal hexamerization domain (Ph1500C) is of particular interest, as it lacks sequence homology to proteins of known structure. However, it resisted crystallization for X-ray analysis, and proteins of this size (49 kDa) present a considerable challenge to NMR structure determination in solution. We solved the high-resolution structure of Ph1500C, exploiting the hyperthermophilic nature of the protein to minimize unfavorable relaxation properties by high-temperature measurement. Thus, the side chain assignment (97%) and structure determination became possible at full proton density. To our knowledge, Ph1500C is the largest protein for which this has been achieved. To minimize detrimental fast water exchange of amide protons at increased temperature, we employed a strategy where the temperature was optimized separately for backbone and side chain experiments

Structural basis for the multiple roles Edc3 plays in mRNA degradation

The Dcp1:Dcp2 decapping complex catalyzes the removal of the protecting 5’ cap structure from mRNA. Adaptor proteins, including Edc3 (enhancer of decapping 3), modulate this decapping process through multiple mechanisms. First, the Edc3 protein enhances the activity of the Dcp2 enzyme directly. Secondly, Edc3 is involved in the formation of cellular processing bodies. Finally, Edc3 is important for the deadenylation independent degradation of the Rps28b mRNA. In the latter case, cellular Rps28b protein levels are regulated through a unique auto-regulatory pathway, where Rps28b that is not in complex with the ribosome binds to a specific stem-loop in the 3’-UTR of its own messenger-RNA. To understand how the Edc3 protein is able to preform these multiple functions, we solved the structure of the yeast Edc3 LSm domain in complex with a short helical leucine-rich motif (HLM) from Dcp2. Based on that structure, we identified additional HLMs in the disordered C-terminal extension of Dcp2 that can interact with Edc3. We show that these multiple HLMs in Dcp2, together with the dimeric nature of Edc3, can lead to the formation of a network of intermolecular interaction. Our experiments thus provide initial insights into one of the mechanisms that underlie processing body formation. Finally, we solved the structure of the Edc3 LSm domain in complex with the Rps28b protein. These data display how the dimeric Edc3 protein is able to bring the Rps28b mRNA and the Dcp1:Dcp2 decapping complex together, thereby targeting the mRNA for degradation. In summary, we show that the Edc3 LSm domain is a plastic platform for multiple protein:protein interactions that are important for the regulation of mRNA degradation