The recombinant dihydropyridine receptor II-III loop and partly structured 'C' region peptides modify cardiac ryanodine receptor activity

A physical association between the II-III loop of the DHPR (dihydroliryidine receptor) and the RyR (ryanodine receptor) is essential for excitation-contraction coupling in skeletal, but not cardiac, muscle. However, peptides corresponding to a part of the II-III loop interact with the cardiac RyR2 suggesting the possibility of a physical coupling between the proteins. Whether the full CI-III loop and its functionally important 'C' region (cardiac OHPR residues 855-891 or skeletal 724-760) interact with carciac RyR2 is not known and is examined in the present study. Both the cardiac DHPR II-III loop (CDCL) and cardiac peptide (C) activated RyR2 channels at concentrations > 10 nM. The skeletal DHPR II-III loop (SDCL) activated channels at less than or equal to 100 nM and weakly inhibited at greater than or equal to 1 muM. In contrast, skeletal peptide (Cs) inhibited channels at all concentrations when added alone, or was ineffective if added in the presence of Cc. Ca2+ induced C2+ release from cardiac sarcoplasmic reticulum was enhanced by CDCL, SDCL and the C pepticles. The results indicate that the interaction between the II-III loop and RyR2 depends critically on the 'A' region (skeletal DHPR residues 67 1 690 or cardiac 793-812) and also involves the C region. Structure analysis indicated that (i) both Cs and Cc are random coil at room temperature, but, at 5 degreesC, have partial helical regions in their N-terminal and central parts, and (ii) secondary -structure profiles for CDCL and SDCL are similar. The data provide novel evidence that the DHPR II-III loop and its C region interact with cardiac RyR2, and that the ability to interact is not isoform-specific.