Mapping the in vitro interactome of cardiac sodium (Na+)-calcium (Ca2+) exchanger 1 (NCX1)

被引:12
作者
Hafver, Tandekile Lubelwana [1 ,2 ]
Wanichawan, Pimthanya [1 ,2 ]
Manfra, Ornella [1 ,2 ]
de Souza, Gustavo Antonio [3 ,4 ,5 ,6 ]
Lunde, Marianne [1 ,2 ]
Martinsen, Marita [1 ,2 ]
Louch, William Edward [1 ,2 ]
Sejersted, Ole Mathias [1 ,2 ]
Carlson, Cathrine Rein [1 ,2 ]
机构
[1] Oslo Univ Hosp, Expt Med Res Inst, Kirkeveien 166, N-0450 Oslo, Norway
[2] Univ Oslo, Oslo, Norway
[3] Univ Oslo, Dept Immunol, Oslo Univ Hosp, HF Rikshosp, Oslo, Norway
[4] Univ Oslo, Ctr Immune Regulat, Oslo Univ Hosp, HF Rikshosp, Oslo, Norway
[5] Univ Fed Rio Grande do Norte, Inst Brain, Natal, RN, Brazil
[6] Univ Fed Rio Grande do Norte, Bioinformat Multidisciplinary Environm Inst Metro, Natal, RN, Brazil
关键词
Cell biology; Heart disease; Interactome; Mass spectrometry; NCX1; Protein-protein interactions; SARCOLEMMAL NA+-CA2+ EXCHANGER; PROTEIN-KINASE-A; LONG-QT SYNDROME; NA+/CA2+ EXCHANGER; HEART-FAILURE; MASS-SPECTROMETRY; MACROMOLECULAR COMPLEX; VENTRICULAR MYOCYTES; DEPENDENT REGULATION; CALCIUM HOMEOSTASIS;
D O I
10.1002/pmic.201600417
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The sodium (Na+)-calcium (Ca2+) exchanger 1 (NCX1) is an antiporter membrane protein encoded by the SLC8A1 gene. In the heart, it maintains cytosolic Ca2+ homeostasis, serving as the primary mechanism for Ca2+ extrusion during relaxation. Dysregulation of NCX1 is observed in end-stage human heart failure. In this study, we used affinity purification coupled with MS in rat left ventricle lysates to identify novel NCX1 interacting proteins in the heart. Two screens were conducted using: (1) anti-NCX1 against endogenous NCX1 and (2) anti-His (where His is histidine) with His-trigger factor-NCX1(cyt) recombinant protein as bait. The respective methods identified 112 and 350 protein partners, of which several were known NCX1 partners from the literature, and 29 occurred in both screens. Ten novel protein partners (DYRK1A, PPP2R2A, SNTB1, DMD, RABGGTA, DNAJB4, BAG3, PDE3A, POPDC2, STK39) were validated for binding to NCX1, and two partners (DYRK1A, SNTB1) increased NCX1 activity when expressed in HEK293 cells. A cardiac NCX1 protein-protein interaction map was constructed. The map was highly connected, containing distinct clusters of proteins with different biological functions, where cell communication and signal transduction formed the largest clusters. The NCX1 interactome was also significantly enriched with proteins/genes involved in cardiovascular disease which can be explored as novel drug targets in future research.
引用
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页数:20
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