Molecular recognition of the disordered dihydropyridine receptor II-III loop by a conserved spry domain of the type 1 ryanodine receptor

Han Shen Tae, Nicole C. Norris, Yanfang Cui, Yamuna Karunasekara, Philip G. Board, Angela F. Dulhunty, Marco G. Casarotto

    Research output: Contribution to journalArticlepeer-review

    16 Citations (Scopus)

    Abstract

    The dihydropyridine receptor (DHPR) II-III loop is an intrinsically unstructured region made up of α-helical and B-turn secondary structure elements with the N and C termini in close spatial proximity. The DHPR II-III loop interacts in vitro with a ryanodine receptor (RyR) 1 SPRY domain through α-helical segments located in the A and B regions. Mutations within the A and B regions in the DHPR II-III loop alter the binding affinity to the SPRY2 domain. The A and C peptides derived from DHPR II-III loop show negative cooperativity in binding to the SPRY2 domain. The SPRY2 domain of the RyR1 (1085-1208) forms a B-sheet sandwich structure flanked by variable loop regions. An acidic loop region of SPRY2 (1107-1121) forms part of a negatively charged cleft that is implicated in the binding of the DHPR II-III loop. The mutant E1108A located in the negatively charged loop of SPRY2 reduces the binding affinity to the DHPR II-III loop.

    Original languageEnglish
    Pages (from-to)346-349
    Number of pages4
    JournalClinical and Experimental Pharmacology and Physiology
    Volume36
    Issue number3
    DOIs
    Publication statusPublished - Mar 2009

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