Decher Niels, Gonzalez Teresa, Streit Anne Kathrin, Sachse Frank B, Renigunta Vijay, Soom Malle, Heinemann Stefan H, Daut Jürgen, Sanguinetti Michael C
Nora Eccles Harrison Cardiovascular Research and Training Institute, University of Utah, Salt Lake City, UT, USA.
EMBO J. 2008 Dec 3;27(23):3164-74. doi: 10.1038/emboj.2008.231. Epub 2008 Nov 6.
Inactivation of voltage-gated Kv1 channels can be altered by Kvbeta subunits, which block the ion-conducting pore to induce a rapid ('N-type') inactivation. Here, we investigate the mechanisms and structural basis of Kvbeta1.3 interaction with the pore domain of Kv1.5 channels. Inactivation induced by Kvbeta1.3 was antagonized by intracellular PIP(2). Mutations of R5 or T6 in Kvbeta1.3 enhanced Kv1.5 inactivation and markedly reduced the effects of PIP(2). R5C or T6C Kvbeta1.3 also exhibited diminished binding of PIP(2) compared with wild-type channels in an in vitro lipid-binding assay. Further, scanning mutagenesis of the N terminus of Kvbeta1.3 revealed that mutations of L2 and A3 eliminated N-type inactivation. Double-mutant cycle analysis indicates that R5 interacts with A501 and T480 of Kv1.5, residues located deep within the pore of the channel. These interactions indicate that Kvbeta1.3, in contrast to Kvbeta1.1, assumes a hairpin structure to inactivate Kv1 channels. Taken together, our findings indicate that inactivation of Kv1.5 is mediated by an equilibrium binding of the N terminus of Kvbeta1.3 between phosphoinositides (PIPs) and the inner pore region of the channel.
电压门控Kv1通道的失活可被Kvβ亚基改变,Kvβ亚基会阻塞离子传导孔以诱导快速(“N型”)失活。在此,我们研究Kvβ1.3与Kv1.5通道孔结构域相互作用的机制和结构基础。Kvβ1.3诱导的失活被细胞内的磷脂酰肌醇-4,5-二磷酸(PIP₂)拮抗。Kvβ1.3中R5或T6的突变增强了Kv1.5的失活,并显著降低了PIP₂的作用。在体外脂质结合试验中,与野生型通道相比,R5C或T6C Kvβ1.3也表现出PIP₂结合减少。此外,对Kvβ1.3 N端的扫描诱变显示,L2和A3的突变消除了N型失活。双突变循环分析表明,R5与Kv1.5的A501和T480相互作用,这些残基位于通道孔的深处。这些相互作用表明,与Kvβ1.1不同,Kvβ1.3呈现发夹结构以使Kv1通道失活。综上所述,我们的研究结果表明,Kv1.5的失活是由Kvβ1.3的N端在磷酸肌醇(PIPs)和通道内孔区域之间的平衡结合介导的。