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Why are they missing? : Bioinformatics characterization of missing human proteins.

Authors :
Elguoshy, Amr
Magdeldin, Sameh
Xu, Bo
Hirao, Yoshitoshi
Zhang, Ying
Kinoshita, Naohiko
Takisawa, Yusuke
Nameta, Masaaki
Yamamoto, Keiko
El-Refy, Ali
El-Fiky, Fawzy
Yamamoto, Tadashi
Source :
Journal of Proteomics. Oct2016, Vol. 149, p7-14. 8p.
Publication Year :
2016

Abstract

NeXtProt is a web-based protein knowledge platform that supports research on human proteins. NeXtProt (release 2015-04-28) lists 20,060 proteins, among them, 3373 canonical proteins (16.8%) lack credible experimental evidence at protein level (PE2:PE5). Therefore, they are considered as “missing proteins”. A comprehensive bioinformatic workflow has been proposed to analyze these “missing” proteins. The aims of current study were to analyze physicochemical properties, existence and distribution of the tryptic cleavage sites, and to pinpoint the signature peptides of the missing proteins. Our findings showed that 23.7% of missing proteins were hydrophobic proteins possessing transmembrane domains (TMD). Also, forty missing entries generate tryptic peptides were either out of mass detection range (> 30 aa) or mapped to different proteins (< 9 aa). Additionally, 21% of missing entries didn't generate any unique tryptic peptides. In silico endopeptidase combination strategy increased the possibility of missing proteins identification. Coherently, using both mature protein database and signal peptidome database could be a promising option to identify some missing proteins by targeting their unique N-terminal tryptic peptide from mature protein database and or C-terminus tryptic peptide from signal peptidome database. In conclusion, Identification of missing protein requires additional consideration during sample preparation, extraction, digestion and data analysis to increase its incidence of identification. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
18743919
Volume :
149
Database :
Academic Search Index
Journal :
Journal of Proteomics
Publication Type :
Academic Journal
Accession number :
119001404
Full Text :
https://doi.org/10.1016/j.jprot.2016.08.005