Metabolic Regulation of the Squid Nerve Na+/Ca2+ Exchanger: Recent Developments

被引:1
作者
Beauge, Luis [1 ]
DiPolo, Reinaldo [2 ]
Bollo, Mariana [1 ]
Cousido, Alexandra [3 ]
Berberian, Graciela [1 ]
Podjarny, Alberto [3 ]
机构
[1] Inst Invest Med Mercedes & Martin Ferreyra INIMEC, Lab Biofis, Cordoba, Argentina
[2] Inst Venezolano Invest Cient, Ctr Biofis, Lab Fisiol, Caracas, Venezuela
[3] Univ Strasbourg, CNRS, INSERM, Dept Struct Biol & Genom,IGBMC, Illkirch Graffenstaden, France
来源
SODIUM CALCIUM EXCHANGE: A GROWING SPECTRUM OF PATHOPHYSIOLOGICAL IMPLICATIONS | 2013年 / 961卷
基金
美国国家科学基金会;
关键词
Na+/Ca2+ exchanger; Metabolic regulation; Regulatory proteins; Lipid-binding protein; Structure-function; Squid nerve; Membrane transport; SODIUM-CALCIUM EXCHANGER; ACID-BINDING PROTEIN; CARDIAC NA+-CA2+ EXCHANGER; ATP-DEPENDENT REGULATION; SODIUM/CALCIUM EXCHANGER; CYTOPLASMIC PROTONS; DYNAMIC PROPERTIES; MGATP STIMULATION; CA2+ REGULATION; STEADY-STATE;
D O I
10.1007/978-1-4614-4756-6_13
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
In squid nerves, MgATP modulation of the Na+/Ca2+ exchanger requires the presence of a cytosolic protein which becomes phosphorylated during the process. This factor has been recently identified. Mass spectroscopy and Western blot analysis established that it is a member of the lipocalin superfamily of lipid-binding proteins (LBP or FABP) of 132 amino acids. We called it regulatory protein of squid nerve sodium/calcium exchanger (ReP1-NCXSQ, access to GenBank EU981897). ReP1-NCXSQ was cloned, expressed, and purified. Circular dichroism, far-UV, and infrared spectroscopy suggest a secondary structure, predominantly of beta-sheets. The tertiary structure prediction provides ten beta-sheets and two alpha-helices, characteristic of most of LPB. Functional experiments showed that, to be active, ReP1-NCXSQ must be phosphorylated by MgATP, through the action of a kinase present in the plasma membrane. Moreover, PO4-ReP1-NCXSQ can stimulate the exchanger in the absence of ATP. An additional crucial observation was that, in proteoliposomes containing only the purified Na+/Ca2+ exchanger, PO4-ReP1-NCXSQ promotes activation; therefore, this upregulation has no other requirement than a lipid membrane and the incorporated exchanger protein. Recently, we solved the crystal structure of ReP1-NCXSQ which was as predicted: a "barrel" consisting of ten beta-sheets and two alpha-helices. Inside the barrel is the fatty acid coordinated by hydrogen bonds with Arg126 and Tyr128. Point mutations showed that neither Tyr20Ala, Arg58Val, Ser99Ala, nor Arg126Val is necessary for protein phosphorylation or activity. On the other hand, Tyr128 is essential for activity but not for phosphorylation. We can conclude that (1) for the first time, a role of an LBP is demonstrated in the metabolic regulation of an ion exchanger; (2) phosphorylation of this LBP can be separated from the activation capacity; and (3) Tyr128, a candidate to coordinate lipid binding inside the barrel, is essential for activity.
引用
收藏
页码:149 / 161
页数:13
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