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Tangible benefits of the aphid Acyrthosiphon pisum genome sequencing for aphid proteomics: Enhancements in protein identification and data validation for homology-based proteomics
Authors:Cilia M  Tamborindeguy C  Rolland M  Howe K  Thannhauser T W  Gray S
Affiliation:a Robert W. Holley Center for Agriculture and Health, Cornell University, Tower Road, Ithaca, NY 14853, USA
b Department of Entomology, Texas A&M University, College Station, TX 77843, USA
c Department of Plant Pathology and Plant Microbe Interactions, Cornell University, Ithaca, NY 14853, USA
Abstract:Homology-driven proteomics promises to reveal functional biology in insects with sparse genome sequence information. A proteomics study comparing plant virus transmission competent and refractive genotypes of the aphid Schizaphis graminum isolated numerous candidate proteins involved in virus transmission, but limited genome sequence information hampered their identification. The complete genome of the pea aphid, Acyrthosiphon pisum, released in 2008, enabled us to double the number of protein identifications beyond what was possible using available EST libraries and other insect sequences. This was concomitant with a dramatic increase of the number of MS and MS/MS peptide spectra matching the genome-derived protein sequence. LC-MS/MS proved to be the most robust method of peptide detection. Cross-matching spectral data to multiple EST sequences and error tolerant searching to identify amino acid substitutions enhanced the percent coverage of the Schizaphis graminum proteins. 2-D electrophoresis provided the protein pI and MW which enabled the refinement of the candidate protein selection and provided a measure of protein abundance when coupled to the spectral data. Thus, the homology-based proteomics pipeline for insects should include efforts to maximize the number of peptide matches to the protein to increase certainty in protein identification and relative protein abundance.
Keywords:Aphid   Proteomics   Homology-driven proteomics   Genome   Virus   EST   Mass spectrometry   2-D gel electrophoresis
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