Structural basis for sarcolipin’s regulation of muscle thermogenesis by the sarcoplasmic reticulum Ca 2+ -ATPase-Reference-Cited by-同舟云学术

Structural basis for sarcolipin’s regulation of muscle thermogenesis by the sarcoplasmic reticulum Ca 2+ -ATPase

Published:2021-11-26 Issue:48 Volume:7 Page:
ISSN:2375-2548
Container-title:Science Advances
language:en
Short-container-title:Sci. Adv.

Author:

Wang Songlin¹^ORCID,Gopinath Tata¹,Larsen Erik K.²,Weber Daniel K.¹,Walker Caitlin¹^ORCID,Uddigiri Venkateswara Reddy¹^ORCID,Mote Kaustubh R.³^ORCID,Sahoo Sanjaya K.⁴,Periasamy Muthu⁴⁵^ORCID,Veglia Gianluigi¹²^ORCID

Affiliation:

1. Department of Biochemistry, Molecular Biology, and Biophysics, University of Minnesota, Minneapolis, MN 55455, USA.

2. Department of Chemistry, University of Minnesota, Minneapolis, MN 55455, USA.

3. Tata Institute of Fundamental Research Hyderabad, Survey No. 36/P Gopanpally, Serilingampally, Ranga Reddy District, Hyderabad, Telangana 500046, India.

4. Department of Physiology, College of Medicine, The Ohio State University, Columbus, OH 43210, USA.

5. Department of Internal Medicine, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.

Abstract

A small peptide regulates muscle thermogenesis through interaction with the sarcoplasmic reticulum calcium ATPase.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference65 articles.

1. Skeletal Muscle: A Brief Review of Structure and Function

2. Sarcolipin is a novel regulator of muscle metabolism and obesity

3. The N Terminus of Sarcolipin Plays an Important Role in Uncoupling Sarco-endoplasmic Reticulum Ca2+-ATPase (SERCA) ATP Hydrolysis from Ca2+ Transport

4. Uncoupling Protein 1 and Sarcolipin Are Required to Maintain Optimal Thermogenesis, and Loss of Both Systems Compromises Survival of Mice under Cold Stress

5. Sarcolipin Is a Key Determinant of the Basal Metabolic Rate, and Its Overexpression Enhances Energy Expenditure and Resistance against Diet-induced Obesity

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