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Principles for applying optogenetic tools derived from direct comparative analysis of microbial opsins

机译:直接从微生物视蛋白进行比较分析得出的光遗传学工具的应用原理

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摘要

Diverse optogenetic tools have allowed versatile control over neural activity. Many depolarizing and hyperpolarizing tools have now been developed in multiple laboratories and tested across different preparations, presenting opportunities but also making it difficult to draw direct comparisons. This challenge has been compounded by the dependence of performance on parameters such as vector, promoter, expression time, illumination, cell type and many other variables. As a result, it has become increasingly complicated for end users to select the optimal reagents for their experimental needs. For a rapidly growing field, critical figures of merit should be formalized both to establish a framework for further development and so that end users can readily understand how these standardized parameters translate into performance. Here we systematically compared microbial opsins under matched experimental conditions to extract essential principles and identify key parameters for the conduct, design and interpretation of experiments involving optogenetic techniques.
机译:各种各样的光遗传学工具已经允许对神经活动进行多功能控制。现在,已经在多个实验室中开发了许多去极化和超极化工具,并在不同的准备工作中对其进行了测试,这不仅带来了机遇,而且也难以进行直接比较。由于性能对参数的依赖,如载体,启动子,表达时间,光照,细胞类型和许多其他变量,使这一挑战更加复杂。结果,最终用户选择最适合他们实验需要的试剂变得越来越复杂。对于一个快速发展的领域,关键的绩效指标应该被正式确定下来,以建立进一步发展的框架,以便最终用户可以容易地理解这些标准化参数如何转化为性能。在这里,我们系统地比较了匹配实验条件下的微生物视蛋白,以提取基本原理并确定关键参数,以进行涉及光遗传学技术的实验,设计和解释。

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