Peptidomic and transcriptomic profiling of four distinct spider venoms

Autor: Dominique Koua, Jean-Luc Wolfender, Vera Oldrati, Wolfgang Nentwig, Miriam Arrell, Pierre-Marie Allard, Reto Stöcklin, Nicolas Hulo, Lucia Kuhn-Nentwig, Frédérique Lisacek
Rok vydání: 2017
Předmět:
0301 basic medicine
Tandem mass spectrometry
Spider Venoms
lcsh:Medicine
Venom
Toxicology
Pathology and Laboratory Medicine
Proteomics
Database and Informatics Methods
Tandem Mass Spectrometry
CSTX
Medicine and Health Sciences
Toxins
lcsh:Science
Structural motif
Peptides metabolism
ddc:615
Multidisciplinary
Spiders
Genomics
Spider venoms metabolism
Sequence Analysis
Transcriptome Analysis
Research Article
Multiple Alignment Calculation
Arthropoda
Bioinformatics
Toxic Agents
Liquid chromatography
Sequence Databases
Sequence alignment
Computational biology
Biology
Research and Analysis Methods
complex mixtures
03 medical and health sciences
Sequence Motif Analysis
Arachnida
Computational Techniques
Genetics
Animals
Venoms
lcsh:R
Organisms
Biology and Life Sciences
Computational Biology
Latrodectus mactans
Genome Analysis
biology.organism_classification
Invertebrates
Split-Decomposition Method
Biological Databases
030104 developmental biology
MRNA Sequencing
lcsh:Q
Peptides
Transcriptome
Sequence Alignment
Chromatography
Liquid
Zdroj: PLoS ONE, Vol 12, Iss 3, p e0172966 (2017)
PLoS ONE
PLOS ONE, Vol. 12, No 3 (2017) P. e0172966
ISSN: 1932-6203
Popis: Venom based research is exploited to find novel candidates for the development of innovative pharmacological tools, drug candidates and new ingredients for cosmetic and agrochemical industries. Moreover, venomics, as a well-established approach in systems biology, helps to elucidate the genetic mechanisms of the production of such a great molecular biodiversity. Today the advances made in the proteomics, transcriptomics and bioinformatics fields, favor venomics, allowing the in depth study of complex matrices and the elucidation even of minor compounds present in minute biological samples. The present study illustrates a rapid and efficient method developed for the elucidation of venom composition based on NextGen mRNA sequencing of venom glands and LC-MS/MS venom proteome profiling. The analysis of the comprehensive data obtained was focused on cysteine rich peptide toxins from four spider species originating from phylogenetically distant families for comparison purposes. The studied species were Heteropoda davidbowie (Sparassidae), Poecilotheria formosa (Theraphosidae), Viridasius fasciatus (Viridasiidae) and Latrodectus mactans (Theridiidae). This led to a high resolution profiling of 284 characterized cysteine rich peptides, 111 of which belong to the Inhibitor Cysteine Knot (ICK) structural motif. The analysis of H. davidbowie venom revealed a high richness in term of venom diversity: 95 peptide sequences were identified; out of these, 32 peptides presented the ICK structural motif and could be classified in six distinct families. The profiling of P. formosa venom highlighted the presence of 126 peptide sequences, with 52 ICK toxins belonging to three structural distinct families. V. fasciatus venom was shown to contain 49 peptide sequences, out of which 22 presented the ICK structural motif and were attributed to five families. The venom of L. mactans, until now studied for its large neurotoxins (Latrotoxins), revealed the presence of 14 cysteine rich peptides, out of which five were ICK toxins belonging to the CSTX superfamily. This in depth profiling of distinct ICK peptide families identified across the four spider species highlighted the high conservation of these neurotoxins among spider families.
Databáze: OpenAIRE