Top-down protein identification of proteasome proteins with nanoLC-FT-ICR-MS employing data-independent fragmentation methods-Reference-Cited by-同舟云学术

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Top-down protein identification of proteasome proteins with nanoLC-FT-ICR-MS employing data-independent fragmentation methods

Published:2014-03-26 Issue:10 Volume:14 Page:1271-1282
ISSN:1615-9853
Container-title:PROTEOMICS
language:en
Short-container-title:Proteomics

Author:

Lakshmanan Rajeswari¹,Wolff Jeremy J.²,Alvarado Rudy¹,Loo Joseph A.¹³

Affiliation:

1. Department of Chemistry and Biochemistry; Molecular Biology Institute; University of California-Los Angeles; Los Angeles CA USA

2. Bruker Daltonics; Billerica MA USA

3. Department of Biological Chemistry; David Geffen School of Medicine at UCLA; University of California-Los Angeles; Los Angeles CA USA

Funder

US National Institutes of Health

Publisher

Wiley

Subject

Molecular Biology,Biochemistry

Reference52 articles.

1. Analysis of protein mixtures from whole-cell extracts by single-run nanoLC-MS/MS using ultralong gradients;Kocher;Nat. Protoc.,2012

2. Recent advances in peptide separation by multidimensional liquid chromatography for proteome analysis;Di Palma;J. Proteomics,2012

3. Automated precursor ion exclusion during LC-MS/MS data acquisition for optimal ion identification;Zhang;J. Am. Soc. Mass Spectrom.,2012

4. Top down versus bottom up protein characterization by tandem high-resolution mass spectrometry;Kelleher;J. Am. Chem. Soc.,1999

5. Primary sequence information from intact proteins by electrospray ionization tandem mass spectrometry;Loo;Science,1990

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