Proteomic analysis provides insights on venom processing in Conus textile.

Conus species of marine snails deliver a potent collection of toxins from the venom duct via a long proboscis attached to a harpoon tooth. Conotoxins are known to possess powerful neurological effects and some have been developed for therapeutic uses. Using mass-spectrometry based proteomics, qualitative and quantitative differences in conotoxin components were found in the proximal, central and distal sections of the Conus textile venom duct suggesting specialization of duct sections for biosynthesis of particular conotoxins. Reversed phase HPLC followed by Orbitrap mass spectrometry and data analysis using SEQUEST and ProLuCID identified 31 conotoxin sequences and 25 post-translational modification (PTM) variants with King-Kong 2 peptide being the most abundant. Several previously unreported variants of known conopeptides were found and this is the first time that HyVal is reported for a disulfide rich Conus peptide. Differential expression along the venom duct, production of PTM variants, alternative proteolytic cleavage sites, and venom processing enroute to the proboscis all appear to contribute to enriching the combinatorial pool of conopeptides and producing the appropriate formulation for a particular hunting situation. The complementary tools of mass spectrometry-based proteomics and molecular biology can greatly accelerate the discovery of Conus peptides and provide insights on envenomation and other biological strategies of cone snails.

[1]  W R Gray,et al.  Peptide neurotoxins from fish-hunting cone snails. , 1985, Science.

[2]  B. Olivera,et al.  Contryphan Is a D-Tryptophan-containing Conus Peptide* , 1996, The Journal of Biological Chemistry.

[3]  Alexander Makarov,et al.  Dynamic range of mass accuracy in LTQ orbitrap hybrid mass spectrometer , 2006, Journal of the American Society for Mass Spectrometry.

[4]  J. Chamot-Rooke,et al.  Fourier transform mass spectrometry: a powerful tool for toxin analysis. , 2006, Toxicon : official journal of the International Society on Toxinology.

[5]  R. Offord,et al.  Comparative proteomic study of the venom of the piscivorous cone snail Conus consors. , 2009, Journal of proteomics.

[6]  J. Yates,et al.  Large-scale analysis of the yeast proteome by multidimensional protein identification technology , 2001, Nature Biotechnology.

[7]  G. Bulaj,et al.  Efficient oxidative folding of conotoxins and the radiation of venomous cone snails , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[8]  A. Smit,et al.  Structural and functional evolution of the vasopressin/oxytocin superfamily: vasopressin-related conopressin is the only member present in Lymnaea, and is involved in the control of sexual behavior , 1995, Journal of Neuroscience.

[9]  A. Burlingame,et al.  Identification of tyrosine sulfation in Conus pennaceus conotoxins α‐PnIA and α‐PnIB: further investigation of labile sulfo‐ and phosphopeptides by electrospray, matrix‐assisted laser desorption/ionization (MALDI) and atmospheric pressure MALDI mass spectrometry , 1999 .

[10]  B. Olivera,et al.  Post-translationally modified neuropeptides from Conus venoms. , 1999, European journal of biochemistry.

[11]  Xin Chen,et al.  Direct cDNA cloning of novel conotoxins of the T-superfamily from Conus textile , 2006, Peptides.

[12]  B. Olivera,et al.  Conus venoms: a rich source of novel ion channel-targeted peptides. , 2004, Physiological reviews.

[13]  M. Wallace,et al.  Intrathecal Ziconotide for Severe Chronic Pain: Safety and Tolerability Results of an Open-Label, Long-Term Trial , 2008, Anesthesia and analgesia.

[14]  J. Yates,et al.  DTASelect and Contrast: tools for assembling and comparing protein identifications from shotgun proteomics. , 2002, Journal of proteome research.

[15]  B. Olivera,et al.  Invertebrate vasopressin/oxytocin homologs. Characterization of peptides from Conus geographus and Conus straitus venoms. , 1987, The Journal of biological chemistry.

[16]  P. Ascenzi,et al.  Conus ventricosus venom peptides profiling by HPLC-MS: a new insight in the intraspecific variation. , 2008, Journal of separation science.

[17]  N. Samatova,et al.  Detecting differential and correlated protein expression in label-free shotgun proteomics. , 2006, Journal of proteome research.

[18]  J. Yates,et al.  A model for random sampling and estimation of relative protein abundance in shotgun proteomics. , 2004, Analytical chemistry.

[19]  G. Bulaj,et al.  Biochemical and gene expression analyses of conotoxins in Conus textile venom ducts. , 2005, Biochemical and biophysical research communications.

[20]  J. McIntosh,et al.  Isolation of Lys-conopressin-G from the venom of the worm-hunting snail, Conus imperialis. , 1994, Toxicon : official journal of the International Society on Toxinology.

[21]  L. Cruz,et al.  Structural and biosynthetic properties of peptides in cone snail venoms , 1995, Peptides.

[22]  Conan K. L. Wang,et al.  ConoServer, a database for conopeptide sequences and structures , 2008, Bioinform..

[23]  Owen M. McDougal,et al.  Definition of the M-conotoxin superfamily: characterization of novel peptides from molluscivorous Conus venoms. , 2005, Biochemistry.

[24]  P. Alewood,et al.  Isolation and characterisation of conomap‐Vt, a d‐amino acid containing excitatory peptide from the venom of a vermivorous cone snail , 2006, FEBS letters.

[25]  J. Sweedler,et al.  Anatomical Correlates of Venom Production in Conus californicus , 2002, The Biological Bulletin.

[26]  D. Yoshikami,et al.  Conus geographus toxins that discriminate between neuronal and muscle sodium channels. , 1985, The Journal of biological chemistry.

[27]  W. Gilly,et al.  The Projectile Tooth of a Fish-Hunting Cone Snail: Conus catus Injects Venom Into Fish Prey Using a High-Speed Ballistic Mechanism , 2004, The Biological Bulletin.

[28]  David Fenyö,et al.  Rapid sensitive analysis of cysteine rich peptide venom components , 2009, Proceedings of the National Academy of Sciences.

[29]  Lu Bai-Song,et al.  Conopeptides from Conus striatus and Conus textile by cDNA cloning☆ , 1999, Peptides.

[30]  A. Kohn,et al.  PRELIMINARY STUDIES ON THE VENOM OF THE MARINE SNAIL CONUS * , 1960, Annals of the New York Academy of Sciences.

[31]  J. McIntosh,et al.  Carboxyglutamate in a Neuroactive Toxin , 2022 .

[32]  A. Kohn PISCIVOROUS GASTROPODS OF THE GENUS CONUS. , 1956, Proceedings of the National Academy of Sciences of the United States of America.

[33]  F. Marí,et al.  A vasopressin/oxytocin-related conopeptide with gamma-carboxyglutamate at position 8. , 2007, The Biochemical journal.

[34]  J. Biggs,et al.  Alpha-conopeptides specifically expressed in the salivary gland of Conus pulicarius. , 2008, Toxicon : official journal of the International Society on Toxinology.

[35]  Hyungwon Choi,et al.  Significance Analysis of Spectral Count Data in Label-free Shotgun Proteomics*S , 2008, Molecular & Cellular Proteomics.

[36]  B. Olivera,et al.  Conus Peptides: Phylogenetic Range of Biological Activity. , 1992, The Biological bulletin.

[37]  Erin M Mitsunaga,et al.  Drugs from slugs--past, present and future perspectives of omega-conotoxin research. , 2010, Chemico-biological interactions.

[38]  G. Fields,et al.  Polypeptide chains containing D-gamma-hydroxyvaline. , 2005, Journal of the American Chemical Society.

[39]  M. Mann,et al.  4. Proteomic Analysis of Posttranslational Modifications , 2013 .

[40]  J. Yates,et al.  An approach to correlate tandem mass spectral data of peptides with amino acid sequences in a protein database , 1994, Journal of the American Society for Mass Spectrometry.

[41]  B. Olivera,et al.  Conantokin-G Precursor and Its Role in γ-Carboxylation by a Vitamin K-dependent Carboxylase from a ConusSnail* , 1998, The Journal of Biological Chemistry.

[42]  J. Gehrmann,et al.  Isolation and characterization of conopeptides by high-performance liquid chromatography combined with mass spectrometry and tandem mass spectrometry. , 1996, Rapid communications in mass spectrometry : RCM.

[43]  S. Woodward,et al.  Constant and hypervariable regions in conotoxin propeptides. , 1990, The EMBO journal.

[44]  K. Lederis,et al.  A vasotocin-like peptide in Aplysia kurodai ganglia: HPLC and RIA evidence for its identity with Lys-conopressin G , 1992, Peptides.

[45]  B. Olivera,et al.  Contulakin-G, an O-Glycosylated Invertebrate Neurotensin* , 1999, The Journal of Biological Chemistry.

[46]  J. Yates,et al.  Performance of a linear ion trap-Orbitrap hybrid for peptide analysis. , 2006, Analytical chemistry.

[47]  G. Bulaj,et al.  Conus peptides - combinatorial chemistry at a cone snail's pace. , 2000, Current opinion in drug discovery & development.

[48]  B. Olivera Conus Venom Peptides: Reflections from the Biology of Clades and Species , 2002 .

[49]  Joshua E. Elias,et al.  Evaluation of multidimensional chromatography coupled with tandem mass spectrometry (LC/LC-MS/MS) for large-scale protein analysis: the yeast proteome. , 2003, Journal of proteome research.

[50]  J. Wilce,et al.  Venom as a source of useful biologically active molecules. , 2001, Emergency medicine.

[51]  J. McIntosh,et al.  The A-superfamily of Conotoxins , 2004, Journal of Biological Chemistry.

[52]  A. Makarov,et al.  The Orbitrap: a new mass spectrometer. , 2005, Journal of mass spectrometry : JMS.

[53]  Brian J. Smith,et al.  Novel conotoxins from Conus striatus and Conus kinoshitai selectively block TTX-resistant sodium channels. , 2005, Biochemistry.

[54]  R. Endean,et al.  FURTHER STUDIES OF THE VENOMS OF CONIDAE. , 1965, Toxicon : official journal of the International Society on Toxinology.

[55]  S. Woodward,et al.  Diversity of Conus neuropeptides. , 1990, Science.

[56]  B. Olivera,et al.  Peptide toxins from Conus geographus venom. , 1981, The Journal of biological chemistry.

[57]  R. Endean,et al.  The venom apparatus of Conus magus. , 1967, Toxicon : official journal of the International Society on Toxinology.

[58]  B. Olivera,et al.  The T-superfamily of Conotoxins* , 1999, The Journal of Biological Chemistry.

[59]  Y. Gilad,et al.  Mechanisms for evolving hypervariability: the case of conopeptides. , 2001, Molecular biology and evolution.