Structural mechanism of cooperative regulation of calcium-sensing receptor-mediated cellular signaling

被引:7
|
作者
Deng, Xiaonan [1 ,2 ]
Xin, Yao [1 ,2 ]
Miller, Cassandra Lynn [1 ,2 ]
Hamelberg, Donald [1 ,2 ]
Kirberger, Michael [3 ]
Moremen, Kelley W. [4 ]
Hu, Jian [5 ]
Yang, Jenny J. [1 ,2 ]
机构
[1] Georgia State Univ, Dept Chem, Ctr Diagnost & Therapeut, Atlanta, GA 30303 USA
[2] Georgia State Univ, Adv Translat Imaging Facil, Atlanta, GA 30303 USA
[3] Georgia Gwinnett Coll, Sch Sci & Technol, Lawrenceville, GA 30043 USA
[4] Univ Georgia, Complex Carbohydrate Res Ctr, 315 Riverbend Rd, Athens, GA 30602 USA
[5] Michigan State Univ, Dept Biochem & Mol Biol, Dept Chem, E Lansing, MI 48824 USA
来源
基金
美国国家科学基金会;
关键词
PREDICTING CA2+-BINDING SITES; EXTRACELLULAR DOMAIN; CA2+-SENSING RECEPTOR; WATER-EXCRETION; RENAL CALCIUM; BINDING-SITE; IDENTIFICATION; ACTIVATION; MUTATIONS; PHOSPHATE;
D O I
10.1016/j.cophys.2020.08.020
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Calcium-sensing receptors (CaSRs) play a central role in regulating extracellular calcium (Ca2+) homeostasis and many (patho)physiological processes. This regulation is primarily orchestrated in response to extracellular stimuli via the extracellular domain (ECD). This paper first reviews the modeled structure of the CaSR ECD and the prediction and investigation of the Ca2+ and amino acid-binding sites. Several recently solved X-ray structures are then compared to support a proposed CaSR activation model involving functional cooperativity. The review also discusses recent implications for drug development. These studies provide new insights into the molecular basis of diseases and the design of therapeutic agents that target CaSR and other family C G protein-coupled receptors (cGPCRs).
引用
收藏
页码:269 / 277
页数:9
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