| Literature DB >> 27535590 |
Wei Wei1, Weijia Luo2, Feilin Wu1,3, Xuehui Peng1,4, Yao Zhang1,5, Manli Zhang1, Yan Zhao1, Na Su1, YingZi Qi1, Lingsheng Chen1, Yangjun Zhang1, Bo Wen6, Fuchu He1, Ping Xu1,2,4.
Abstract
Since 2012, missing proteins (MPs) investigation has been one of the critical missions of Chromosome-Centric Human Proteome Project (C-HPP) through various biochemical strategies. On the basis of our previous testis MPs study, faster scanning and higher resolution mass-spectrometry-based proteomics might be conducive to MPs exploration, especially for low-abundance proteins. In this study, Q-Exactive HF (HF) was used to survey proteins from the same testis tissues separated by two separating methods (tricine- and glycine-SDS-PAGE), as previously described. A total of 8526 proteins were identified, of which more low-abundance proteins were uniquely detected in HF data but not in our previous LTQ Orbitrap Velos (Velos) reanalysis data. Further transcriptomics analysis showed that these uniquely identified proteins by HF also had lower expression at the mRNA level. Of the 81 total identified MPs, 74 and 39 proteins were listed as MPs in HF and Velos data sets, respectively. Among the above MPs, 47 proteins (43 neXtProt PE2 and 4 PE3) were ranked as confirmed MPs after verifying with the stringent spectra match and isobaric and single amino acid variants filtering. Functional investigation of these 47 MPs revealed that 11 MPs were testis-specific proteins and 7 MPs were involved in spermatogenesis process. Therefore, we concluded that higher scanning speed and resolution of HF might be factors for improving the low-abundance MP identification in future C-HPP studies. All mass-spectrometry data from this study have been deposited in the ProteomeXchange with identifier PXD004092.Entities:
Keywords: Chromosome-Centric Human Proteome Project; LTQ Orbitrap Velos; Q-Exactive HF; missing proteins; testis
Mesh:
Substances:
Year: 2016 PMID: 27535590 DOI: 10.1021/acs.jproteome.6b00390
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466