The Human Plasma Proteome Draft of 2017: Building on the Human Plasma PeptideAtlas from Mass Spectrometry and Complementary Assays.
The Human Plasma Proteome Draft of 2017: Building on the Human Plasma PeptideAtlas from Mass Spectrometry and Complementary Assays.
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DOI:
10.1021/acs.jproteome.7b00467
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发表时间:
2017-12-01
影响因子:
4.4
通讯作者:
Deutsch EW
中科院分区:
文献类型:
--
作者:
Schwenk JM;Omenn GS;Sun Z;Campbell DS;Baker MS;Overall CM;Aebersold R;Moritz RL;Deutsch EW
Human blood plasma provides a highly accessible window to the proteome of any individual in health and disease. Since its inception in 2002, the Human Proteome Organization’s Human Plasma Proteome Project (HPPP) has been promoting advances in the study and understanding of the full protein complement of human plasma and on determining the abundance and modifications of its components. In 2017, we review the history of the HPPP and the advances of human plasma proteomics in general, including several recent achievements. We then present the latest 2017-04 build of Human Plasma PeptideAtlas, which yields ~43 million peptide-spectrum matches and 122,730 distinct peptide sequences from 178 individual experiments at a 1% protein-level FDR globally across all experiments. Applying the latest Human Proteome Project Data Interpretation Guidelines, we catalog 3509 proteins that have at least two non-nested uniquely-mapping peptides of 9 amino acids or more and >1300 additional proteins with ambiguous evidence. We apply the same two-peptide guideline to historical PeptideAtlas builds going back to 2006 and examine the progress made in the past ten years in plasma proteome coverage. We also compare the distribution of proteins in historical PeptideAtlas builds in various RNA-abundance and cellular localization categories. We then discuss advances in plasma proteomics based on targeted mass spectrometry as well as affinity assays, which during early 2017 target ~2000 proteins. Finally we describe considerations about sample handling and study design, concluding with an outlook for future advances in deciphering the human plasma proteome.
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影响因子:
3.4
作者:
Deutsch, Eric W.;Mendoza, Luis;Shteynberg, David;Farrah, Terry;Lam, Henry;Tasman, Natalie;Sun, Zhi;Nilsson, Erik;Pratt, Brian;Prazen, Bryan;Eng, Jimmy K.;Martin, Daniel B.;Nesvizhskii, Alexey I.;Aebersold, Ruedi
通讯作者:
Aebersold, Ruedi
DOI:
10.1007/978-1-61779-068-3_23
发表时间:
2011-01-01
期刊:
SERUM/PLASMA PROTEOMICS: METHODS AND PROTOCOLS
影响因子:
--
作者:
Farrah, Terry;Deutsch, Eric W.;Aebersold, Ruedi
通讯作者:
Aebersold, Ruedi
影响因子:
4.4
作者:
Anderson, NL;Anderson, NG;Pearson, TW
通讯作者:
Pearson, TW
影响因子:
3.4
作者:
Deutsch, EW;Eng, JK;Aebersold, R
通讯作者:
Aebersold, R
影响因子:
4.4
作者:
Deutsch EW;Overall CM;Van Eyk JE;Baker MS;Paik YK;Weintraub ST;Lane L;Martens L;Vandenbrouck Y;Kusebauch U;Hancock WS;Hermjakob H;Aebersold R;Moritz RL;Omenn GS
通讯作者:
Omenn GS