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基于CRY2-CIB1系统的光调节蛋白激酶

Light-Regulated Protein Kinases Based on the CRY2-CIB1 System.

作者信息

Mühlhäuser Wignand W D, Hörner Maximilian, Weber Wilfried, Radziwill Gerald

机构信息

Faculty of Biology and BIOSS - Centre for Biological Signalling Studies, University of Freiburg, Schänzlestr. 18, 79104, Freiburg, Germany.

出版信息

Methods Mol Biol. 2017;1596:257-270. doi: 10.1007/978-1-4939-6940-1_16.

Abstract

Optogenetic approaches enable the control of biological processes in a time- and space-resolved manner. These light-based methods are noninvasive and by using light as sole activator minimize side effects in contrast to chemical inducers. Here, we provide a protocol for the targeted control of the activity of protein kinases in mammalian cells based on the photoreceptor cryptochrome 2 (CRY2) of Arabidopsis thaliana and its interaction partner CIB1. Blue light (450 nm)-induced binding of CRY2 to CIB1 allows the recruitment of a chimeric cytosolic protein kinase AKT1 to the plasma membrane accompanied with stimulation of its kinase activity. This protocol comprises the transient and stable implementation of the light-regulated system into mammalian cells and its stimulation by blue light-emitting diodes (450 nm) irradiation as well as analysis of the light-activated AKT1.

摘要

光遗传学方法能够以时间和空间分辨的方式控制生物过程。这些基于光的方法是非侵入性的,与化学诱导剂相比,通过仅使用光作为激活剂将副作用降至最低。在此,我们提供了一种基于拟南芥光受体隐花色素2(CRY2)及其相互作用伴侣CIB1,在哺乳动物细胞中靶向控制蛋白激酶活性的方案。蓝光(450nm)诱导CRY2与CIB1结合,使得嵌合的胞质蛋白激酶AKT1募集到质膜,并伴随其激酶活性的刺激。该方案包括将光调节系统瞬时和稳定地导入哺乳动物细胞,通过蓝光发光二极管(450nm)照射对其进行刺激,以及对光激活的AKT1进行分析。

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