scholarly journals Research on the Human Proteome Reaches a Major Milestone: >90% of Predicted Human Proteins Now Credibly Detected, According to the HUPO Human Proteome Project

2020 ◽  
Vol 19 (12) ◽  
pp. 4735-4746 ◽  
Author(s):  
Gilbert S. Omenn ◽  
Lydie Lane ◽  
Christopher M. Overall ◽  
Ileana M. Cristea ◽  
Fernando J. Corrales ◽  
...  
2019 ◽  
Author(s):  
Eric W. Deutsch ◽  
Lydie Lane ◽  
Christopher M. Overall ◽  
Nuno Bandeira ◽  
Mark S. Baker ◽  
...  

AbstractThe Human Proteome Organization’s (HUPO) Human Proteome Project (HPP) developed Mass Spectrometry (MS) Data Interpretation Guidelines that have been applied since 2016. These guidelines have helped ensure that the emerging draft of the complete human proteome is highly accurate and with low numbers of false-positive protein identifications. Here, we describe an update to these guidelines based on consensus-reaching discussions with the wider HPP community over the past year. The revised 3.0 guidelines address several major and minor identified gaps. We have added guidelines for emerging data independent acquisition (DIA) MS workflows and for use of the new Universal Spectrum Identifier (USI) system being developed by the HUPO Proteomics Standards Initiative (PSI). In addition, we discuss updates to the standard HPP pipeline for collecting MS evidence for all proteins in the HPP, including refinements to minimum evidence. We present a new plan for incorporating MassIVE-KB into the HPP pipeline for the next (HPP 2020) cycle in order to obtain more comprehensive coverage of public MS data sets. The main checklist has been reorganized under headings and subitems and related guidelines have been grouped. In sum, Version 2.1 of the HPP MS Data Interpretation Guidelines has served well and this timely update to version 3.0 will aid the HPP as it approaches its goal of collecting and curating MS evidence of translation and expression for all predicted ∼20,000 human proteins encoded by the human genome.Abstract Figure


PROTEOMICS ◽  
2010 ◽  
Vol 10 (17) ◽  
pp. 3067-3072 ◽  
Author(s):  
Thierry Rabilloud ◽  
Denis Hochstrasser ◽  
Richard J. Simpson

Author(s):  
Gilbert S. Omenn ◽  
Lydie Lane ◽  
Christopher M. Overall ◽  
Young-Ki Paik ◽  
Ileana M. Cristea ◽  
...  

2017 ◽  
Vol 16 (12) ◽  
pp. 4281-4287 ◽  
Author(s):  
Gilbert S. Omenn ◽  
Lydie Lane ◽  
Emma K. Lundberg ◽  
Christopher M. Overall ◽  
Eric W. Deutsch

eLife ◽  
2016 ◽  
Vol 5 ◽  
Author(s):  
José Ignacio Garzón ◽  
Lei Deng ◽  
Diana Murray ◽  
Sagi Shapira ◽  
Donald Petrey ◽  
...  

We present a database, PrePPI (Predicting Protein-Protein Interactions), of more than 1.35 million predicted protein-protein interactions (PPIs). Of these at least 127,000 are expected to constitute direct physical interactions although the actual number may be much larger (~500,000). The current PrePPI, which contains predicted interactions for about 85% of the human proteome, is related to an earlier version but is based on additional sources of interaction evidence and is far larger in scope. The use of structural relationships allows PrePPI to infer numerous previously unreported interactions. PrePPI has been subjected to a series of validation tests including reproducing known interactions, recapitulating multi-protein complexes, analysis of disease associated SNPs, and identifying functional relationships between interacting proteins. We show, using Gene Set Enrichment Analysis (GSEA), that predicted interaction partners can be used to annotate a protein’s function. We provide annotations for most human proteins, including many annotated as having unknown function.


2020 ◽  
Vol 19 (12) ◽  
pp. 4747-4753
Author(s):  
Mehdi Alikhani ◽  
Razieh Karamzadeh ◽  
Pardis Rahimi ◽  
Samane Adib ◽  
Hossein Baharvand ◽  
...  

Biochimie ◽  
2016 ◽  
Vol 122 ◽  
pp. 110-118 ◽  
Author(s):  
Ulrich Eckhard ◽  
Giada Marino ◽  
Georgina S. Butler ◽  
Christopher M. Overall

2017 ◽  
Vol 16 (12) ◽  
pp. 4253-4258 ◽  
Author(s):  
Young-Ki Paik ◽  
Christopher M. Overall ◽  
Eric W. Deutsch ◽  
Jennifer E. Van Eyk ◽  
Gilbert S. Omenn

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