AI Article Synopsis

  • - The sodium-calcium exchanger 1 (NCX1) helps regulate calcium levels in the heart and is crucial for heart relaxation; its dysfunction is linked to severe heart failure.
  • - Researchers used advanced techniques to identify new proteins that interact with NCX1 in rat heart tissue, resulting in the discovery of 462 potential protein partners, with ten being novel and two enhancing NCX1 activity.
  • - A detailed interaction map of NCX1 was created, revealing clusters of proteins involved in "cell communication" and "signal transduction," indicating potential novel targets for drugs related to cardiovascular diseases.

Article Abstract

The sodium (Na )-calcium (Ca ) exchanger 1 (NCX1) is an antiporter membrane protein encoded by the SLC8A1 gene. In the heart, it maintains cytosolic Ca homeostasis, serving as the primary mechanism for Ca 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 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.

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http://dx.doi.org/10.1002/pmic.201600417DOI Listing

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