| Literature DB >> 28891297 |
Christine Carapito1, Paula Duek2, Charlotte Macron1, Marine Seffals3, Karine Rondel4, François Delalande1, Cecilia Lindskog5, Thomas Fréour6,7, Yves Vandenbrouck8,9,10, Lydie Lane2,11, Charles Pineau4.
Abstract
The present study is a contribution to the "neXt50 challenge", a coordinated effort across C-HPP teams to identify the 50 most tractable missing proteins (MPs) on each chromosome. We report the targeted search of 38 theoretically detectable MPs from chromosomes 2 and 14 in Triton X-100 soluble and insoluble sperm fractions from a total of 15 healthy donors. A targeted mass-spectrometry-based strategy consisting of the development of LC-PRM assays (with heavy labeled synthetic peptides) targeting 92 proteotypic peptides of the 38 selected MPs was used. Out of the 38 selected MPs, 12 were identified with two or more peptides and 3 with one peptide after extensive SDS-PAGE fractionation of the two samples and with overall low-intensity signals. The PRM data are available via ProteomeXchange in PASSEL (PASS01013). Further validation by immunohistochemistry on human testes sections and cytochemistry on sperm smears was performed for eight MPs with antibodies available from the Human Protein Atlas. Deep analysis of human sperm still allows the validation of MPs and therefore contributes to the C-HPP worldwide effort. We anticipate that our results will be of interest to the reproductive biology community because an in-depth analysis of these MPs may identify potential new candidates in the context of human idiopathic infertilities.Entities:
Keywords: bioinformatics; data mining; human proteome project; immunocytochemistry; immunohistochemistry; missing proteins; parallel reaction monitoring; spermatozoon; targeted proteomics
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Year: 2017 PMID: 28891297 DOI: 10.1021/acs.jproteome.7b00374
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466