| First Author | Mi T | Year | 2015 |
| Journal | Biochem J | Volume | 467 |
| Issue | 1 | Pages | 177-90 |
| PubMed ID | 25605235 | Mgi Jnum | J:221370 |
| Mgi Id | MGI:5638981 | Doi | 10.1042/BJ20141263 |
| Citation | Mi T, et al. (2015) Role of Cys(3)(6)(0)(2) in the function and regulation of the cardiac ryanodine receptor. Biochem J 467(1):177-90 |
| abstractText | The cardiac Ca(2)(+) release channel [ryanodine receptor type 2 (RyR2)] is modulated by thiol reactive agents, but the molecular basis of RyR2 modulation by thiol reagents is poorly understood. Cys(3)(6)(3)(5) in the skeletal muscle RyR1 is one of the most hyper-reactive thiols and is important for the redox and calmodulin (CaM) regulation of the RyR1 channel. However, little is known about the role of the corresponding cysteine residue in RyR2 (Cys(3)(6)(0)(2)) in the function and regulation of the RyR2 channel. In the present study, we assessed the impact of mutating Cys(3)(6)(0)(2) (C(3)(6)(0)(2)A) on store overload-induced Ca(2)(+) release (SOICR) and the regulation of RyR2 by thiol reagents and CaM. We found that the C(3)(6)(0)(2)A mutation suppressed SOICR by raising the activation threshold and delayed the termination of Ca(2)(+) release by reducing the termination threshold. As a result, C(3)(6)(0)(2)A markedly increased the fractional Ca(2)(+) release. Furthermore, the C(3)(6)(0)(2)A mutation diminished the inhibitory effect of N-ethylmaleimide on Ca(2)(+) release, but it had no effect on the stimulatory action of 4,4'-dithiodipyridine (DTDP) on Ca(2)(+) release. In addition, Cys(3)(6)(0)(2) mutations (C(3)(6)(0)(2)A or C(3)(6)(0)(2)R) did not abolish the effect of CaM on Ca(2)(+)-release termination. Therefore, RyR2-Cys(3)(6)(0)(2) is a major site mediating the action of thiol alkylating agent N-ethylmaleimide, but not the action of the oxidant DTDP. Our data also indicate that residue Cys(3)(6)(0)(2) plays an important role in the activation and termination of Ca(2)(+) release, but it is not essential for CaM regulation of RyR2. |
