Differential evolution and neofunctionalization of snake venom metalloprotease domains

A Brust, Kartik Sunagar, Elvind A B Undheim, Irina Vetter, Daryl Yang, Nicholas R Casewell, Timothy N W Jackson, Ivan Koludarov, Paul F Alewood, Wayne Clarence Hodgson, Richard J Lewis, Glenn F King, Agostinho Antunes, Iwan Hendrikx, Bryan G Fry

Research output: Contribution to journalArticleResearchpeer-review

53 Citations (Scopus)

Abstract

Snake venom metalloproteases (SVMP) are composed of five domains: signal peptide, propeptide, metalloprotease, disintegrin, and cysteine-rich. Secreted toxins are typically combinatorial variations of the latter three domains. The SVMP-encoding genes of Psammophis mossambicus venom are unique in containing only the signal and propeptide domains. We show that the Psammophis SVMP propeptide evolves rapidly and is subject to a high degree of positive selection. Unlike Psammophis, some species of Echis express both the typical multidomain and the unusual monodomain (propeptide only) SVMP, with the result that a lower level of variation is exerted upon the latter. We showed that most mutations in the multidomain Echis SVMP occurred in the protease domain responsible for proteolytic and hemorrhagic activities. The cysteine-rich and disintegrin-like domains, which are putatively responsible for making the P-III SVMPs more potent than the P-I and P-II forms, accumulate the remaining variation. Thus, the binding sites on the molecule s surface are evolving rapidly whereas the core remains relatively conserved. Bioassays conducted on two post-translationally cleaved novel proline-rich peptides from the P. mossambicus propeptide domain showed them to have been neofunctionalized for specific inhibition of mammalian a7 neuronal nicotinic acetylcholine receptors. We show that the proline rich postsynaptic specific neurotoxic peptides from Azemiops feae are the result of convergent evolution within the precursor region of the C-type natriuretic peptide instead of the SVMP. The results of this study reinforce the value of studying obscure venoms for biodiscovery of novel investigational ligands.
Original languageEnglish
Pages (from-to)651 - 663
Number of pages13
JournalMolecular & Cellular Proteomics
Volume12
Issue number3
DOIs
Publication statusPublished - 2013

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