Deep Intact Proteoform Characterization in Human Cell Lysate Using High-pH and Low-pH Reversed-Phase Liquid Chromatography-Reference-Cited by-同舟云学术

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Deep Intact Proteoform Characterization in Human Cell Lysate Using High-pH and Low-pH Reversed-Phase Liquid Chromatography

Published:2019-11-21 Issue:12 Volume:30 Page:2502-2513
ISSN:1044-0305
Container-title:Journal of the American Society for Mass Spectrometry
language:en
Short-container-title:J. Am. Soc. Mass Spectrom.

Author:

Yu Dahang¹,Wang Zhe¹,Cupp-Sutton Kellye A.¹,Liu Xiaowen²,Wu Si¹

Affiliation:

1. Department of Chemistry and Biochemistry, University of Oklahoma, 101 Stephenson Parkway, Room 2210, 73019-5251, Norman, OK, USA

2. School of Informatics and Computing, Indiana University-Purdue University Indianapolis, 46202, Indianapolis, IN, USA

Funder

National Institute of Allergy and Infectious Diseases

National Institute of General Medical Sciences

University of Oklahoma

Oklahoma Center for the Advancement of Science and Technology

Publisher

American Chemical Society (ACS)

Subject

Spectroscopy,Structural Biology

Link

http://link.springer.com/content/pdf/10.1007/s13361-019-02315-2.pdf

Reference63 articles.

1. Role of the alpha-amino group of protein in ubiquitin-mediated protein breakdown.

2. Histone chaperone Asf1 is required for histone H3 lysine 56 acetylation, a modification associated with S phase in mitosis and meiosis

3. Histone acetylation in chromatin structure and transcription

4. Extensive lysine acetylation occurs in evolutionarily conserved metabolic pathways and parasite-specific functions duringPlasmodium falciparumintraerythrocytic development

5. Mass spectrometry identifies and quantifies 74 unique histone H4 isoforms in differentiating human embryonic stem cells

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