Enhanced Identification of Zero-Length Chemical Cross-Links Using Label-Free Quantitation and High-Resolution Fragment Ion Spectra-Reference-Cited by-同舟云学术

Enhanced Identification of Zero-Length Chemical Cross-Links Using Label-Free Quantitation and High-Resolution Fragment Ion Spectra

Published:2014-01-07 Issue:2 Volume:13 Page:898-914
ISSN:1535-3893
Container-title:Journal of Proteome Research
language:en
Short-container-title:J. Proteome Res.

Author:

Sriswasdi Sira¹²,Harper Sandra L.¹,Tang Hsin-Yao¹,Speicher David W.¹²

Affiliation:

1. Center for Systems and Computational Biology and Molecular and Cellular Oncogenesis Program, The Wistar Institute, 3601 Spruce Street, Philadelphia, Pennsylvania 19104, United States

2. Genomics and Computational Biology Graduate Group, University of Pennsylvania, 1420 Blockley Hall, 423 Guardian Drive, Philadelphia, Pennsylvania 19104, United States

Publisher

American Chemical Society (ACS)

Subject

General Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/pr400953w

Reference50 articles.

1. A Generic Strategy To Analyze the Spatial Organization of Multi-Protein Complexes by Cross-Linking and Mass Spectrometry

2. High throughput protein fold identification by using experimental constraints derived from intramolecular cross-links and mass spectrometry

3. Architecture of the RNA polymerase II–TFIIF complex revealed by cross-linking and mass spectrometry

4. Molecular architecture of the 26S proteasome holocomplex determined by an integrative approach

5. The Molecular Architecture of the Eukaryotic Chaperonin TRiC/CCT

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