Insights into the molecular basis of the palmitoylation and depalmitoylation of NCX1

Caglar Gök, Alice Main, Xing Gao, Zsombor Kerekes, Fiona Plain, Chien-Wen Kuo, Alan D. Robertson, Niall J. Fraser, William Fuller (Lead / Corresponding author)

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Catalyzed by zDHHC-PAT enzymes and reversed by thioesterases, protein palmitoylation is the only post-translational modification recognized to regulate the sodium/calcium exchanger NCX1. NCX1 palmitoylation occurs at a single site at position 739 in its large regulatory intracellular loop. An amphipathic ɑ-helix between residues 740–756 is a critical for NCX1 palmitoylation. Given the rich background of the structural elements involving in NCX1 palmitoylation, the molecular basis of NCX1 palmitoylation is still relatively poorly understood. Here we found that (1) the identity of palmitoylation machinery of NCX1 controls its spatial organization within the cell, (2) the NCX1 amphipathic ɑ-helix directly interacts with zDHHC-PATs, (3) NCX1 is still palmitoylated when it is arrested in either Golgi or ER, indicating that NCX1 is a substrate for multiple zDHHC-PATs, (4) the thioesterase APT1 but not APT2 as a part of NCX1-depalmitoylation machinery governs subcellular organization of NCX1, (5) APT1 catalyzes NCX1 depalmitoylation in the Golgi but not in the ER. We also report that NCX2 and NCX3 are dually palmitoylated, with important implications for substrate recognition and enzyme catalysis by zDHHC-PATs. Our results could support new molecular or pharmacological strategies targeting the NCX1 palmitoylation and depalmitoylation machinery.

    Original languageEnglish
    Article number102408
    Number of pages10
    JournalCell Calcium
    Volume97
    Early online date8 Apr 2021
    DOIs
    Publication statusE-pub ahead of print - 8 Apr 2021

    Keywords

    • APT1
    • Depalmitoylation
    • NCX1
    • Palmitoylation
    • Thioesterase
    • zDHHC-PATs

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