Phosphorylation Sites of the Gastric Inhibitory Polypeptide Receptor (GIPR) Revealed by Trapped-Ion-Mobility Spectrometry Coupled to Time-of-Flight Mass Spectrometry (TIMS-TOF MS)-Reference-Cited by-同舟云学术

Phosphorylation Sites of the Gastric Inhibitory Polypeptide Receptor (GIPR) Revealed by Trapped-Ion-Mobility Spectrometry Coupled to Time-of-Flight Mass Spectrometry (TIMS-TOF MS)

Published:2023-12-13 Issue:51 Volume:145 Page:28030-28037
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Brown Kyle A.¹^ORCID,Morris Rylie K.¹^ORCID,Eckhardt Samantha J.¹²,Ge Ying¹³^ORCID,Gellman Samuel H.¹^ORCID

Affiliation:

1. Department of Chemistry, University of Wisconsin−Madison, Madison, Wisconsin 53706, United States

2. Department of Cell and Regenerative Biology, University of Wisconsin−Madison, Madison, Wisconsin 53705, United States

3. Human Proteomics Program, School of Medicine and Public Health, University of Wisconsin−Madison, Madison, Wisconsin 53705, United States

Funder

William F. Vilas Trust Estate

National Institutes of Health

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.3c09078

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1. G protein-coupled receptors: structure- and function-based drug discovery

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4. Distinct Phosphorylation Sites on the β 2 -Adrenergic Receptor Establish a Barcode That Encodes Differential Functions of β-Arrestin

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