Szundi Istvan, Bogomolni Roberto, Kliger David S
From the Department of Chemistry and Biochemistry, University of California, Santa Cruz, California 95064.
From the Department of Chemistry and Biochemistry, University of California, Santa Cruz, California 95064
J Biol Chem. 2015 Jul 3;290(27):16585-94. doi: 10.1074/jbc.M115.653071. Epub 2015 May 13.
Channelrhodopsins, such as the algal phototaxis receptor Platymonas subcordiformis channelrhodopsin-2 (PsChR2), are light-gated cation channels used as optogenetic tools for photocontrol of membrane potential in living cells. Channelrhodopsin (ChR)-mediated photocurrent responses are complex and poorly understood, exhibiting alterations in peak current amplitude, extents and kinetics of inactivation, and kinetics of the recovery of the prestimulus dark current that are sensitive to duration and frequency of photostimuli. From the analysis of time-resolved optical absorption data, presented in the accompanying article, we derived a two-cycle model that describes the photocycles of PsChR2. Here, we applied the model to evaluate the transient currents produced by PsChR2 expressed in HEK293 cells under both fast laser excitation and step-like continuous illumination. Interpretation of the photocurrents in terms of the photocycle kinetics indicates that the O states in both cycles are responsible for the channel current and fit the current transients under the different illumination regimes. The peak and plateau currents in response to a single light step, a train of light pulses, and a light step superimposed on a continuous light background observed for ChR2 proteins are explained in terms of contributions from the two parallel photocycles. The analysis shows that the peak current desensitization and recovery phenomena are inherent properties of the photocycles. The light dependence of desensitization is reproduced and explained by the time evolution of the concentration transients in response to step-like illumination. Our data show that photocycle kinetic parameters are sufficient to explain the complex dependence of photocurrent responses to photostimuli.
通道视紫红质,如藻类趋光性受体亚心形扁藻通道视紫红质-2(PsChR2),是光门控阳离子通道,用作光遗传学工具,用于光控活细胞中的膜电位。通道视紫红质(ChR)介导的光电流响应很复杂,人们对此了解甚少,其峰值电流幅度、失活程度和动力学以及刺激前暗电流恢复动力学都会发生变化,这些变化对光刺激的持续时间和频率敏感。通过对随附文章中给出的时间分辨光吸收数据进行分析,我们得出了一个描述PsChR2光循环的双循环模型。在此,我们应用该模型评估在快速激光激发和阶梯状连续光照下,HEK293细胞中表达的PsChR2产生的瞬态电流。根据光循环动力学对光电流进行解释表明,两个循环中的O状态都与通道电流有关,并符合不同光照条件下的电流瞬变。针对ChR2蛋白观察到的单个光脉冲、一串光脉冲以及叠加在连续光背景上的单个光脉冲所产生的峰值电流和平顶电流,根据两个平行光循环的贡献进行了解释。分析表明,峰值电流脱敏和恢复现象是光循环的固有特性。脱敏的光依赖性通过响应阶梯状光照的浓度瞬变的时间演化得以再现和解释。我们的数据表明,光循环动力学参数足以解释光电流响应对光刺激的复杂依赖性。