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KV4.3 N-terminal deletion mutant Δ2–39

机译:KV4.3 N端缺失突变体Δ2-39

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摘要

Gating transitions in the KV4.3 N-terminal deletion mutant Δ2–39 were characterized in the absence and presence of KChIP2b. We particularly focused on gating characteristics of macroscopic (open state) versus closed state inactivation (CSI) and recovery. In the absence of KChIP2b Δ2–39 did not significantly alter the steady-state activation “a4” relationship or general CSI characteristics, but it did slow the kinetics of deactivation, macroscopic inactivation and macroscopic recovery. Recovery kinetics (for both WT KV4.3 and Δ2–39) were complicated and displayed sigmoidicity, a process which was enhanced by Δ2–39. Deletion of the proximal N-terminal domain therefore appeared to specifically slow mechanisms involved in regulating gating transitions occurring after the channel open state(s) had been reached. In the presence of KChIP2b Δ2–39 recovery kinetics (from both macroscopic and CSI) were accelerated, with an apparent reduction in initial sigmoidicity. Hyperpolarizing shifts in both “a4” and isochronal inactivation “i” were also produced. KChIP2b-mediated remodeling of KV4.3 gating transitions was therefore not obligatorily dependent upon an intact N-terminus. To account for these effects we propose that KChIP2 regulatory domains exist in KV4.3 α subunit regions outside of the proximal N-terminal. In addition to regulating macroscopic inactivation, we also propose that the KV4.3 N-terminus may act as a novel regulator of deactivation-recovery coupling.
机译:在不存在和存在KChIP2b的情况下,对KV4.3 N端缺失突变体Δ2-39的门控转换进行了表征。我们特别关注宏观(打开状态)与关闭状态灭活(CSI)和恢复的门控特性。在没有KChIP2b的情况下,Δ2-39不会显着改变稳态激活“ a 4 ”关系或一般CSI特性,但会减慢失活,宏观失活和宏观恢复的动力学。恢复动力学(对于WT KV4.3和Δ2-39)很复杂且显示出乙状结肠,此过程被Δ2-39增强。因此,近端N末端结构域的缺失似乎特别缓慢地参与了调节在达到通道开放状态之后发生的门控转变的机制。在存在KChIP2b Δ2–39的情况下,恢复动力学(从宏观和CSI方面)都得到了加速,初始Sigmoidicity明显降低。同时产生“ a 4 ”和等时失活“ i”的超极化转变。因此,KChIP2b介导的KV4.3门控转换的重塑不是强制性地依赖于完整的N末端。为了说明这些影响,我们建议在近端N末端之外的KV4.3α亚基区域中存在KChIP2调节域。除了调节宏观失活外,我们还建议KV4.3 N端可作为失活-恢复偶联的新型调节剂。

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