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Structural basis of the transmembrane domain dimerization and rotation in the activation mechanism of the TRKA receptor by nerve growth factor.神经生长因子激活 TRKA 受体的跨膜结构域二聚化和旋转的结构基础。
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Fluorescent Biosensors for Neurotransmission and Neuromodulation: Engineering and Applications.用于神经传递和神经调节的荧光生物传感器:工程与应用
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Emerging Allosteric Mechanism of EGFR Activation in Physiological and Pathological Contexts.在生理和病理环境下,EGFR 激活的新兴别构机制。
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Neurotrophin receptor tyrosine kinases regulated with near-infrared light.神经营养因子受体酪氨酸激酶的近红外光调控。
Nat Commun. 2019 Mar 8;10(1):1129. doi: 10.1038/s41467-019-08988-3.
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Fibroblast growth factor receptors as treatment targets in clinical oncology.成纤维细胞生长因子受体作为临床肿瘤学的治疗靶点。
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Monitoring hippocampal glycine with the computationally designed optical sensor GlyFS.使用计算设计的光学传感器 GlyFS 监测海马甘氨酸。
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Near-infrared light-controlled systems for gene transcription regulation, protein targeting and spectral multiplexing.近红外光控制的基因转录调控、蛋白质靶向和光谱复用系统。
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Optogenetically controlled protein kinases for regulation of cellular signaling.用于调节细胞信号传导的光遗传学控制蛋白激酶
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Near-Infrared Fluorescent Proteins, Biosensors, and Optogenetic Tools Engineered from Phytochromes.基于光敏色素的近红外荧光蛋白、生物传感器和光遗传学工具。
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细菌光受体作为一种支架,用于工程化受近红外光调控的受体酪氨酸激酶。

Bacterial Phytochrome as a Scaffold for Engineering of Receptor Tyrosine Kinases Controlled with Near-Infrared Light.

机构信息

Medicum, Faculty of Medicine, University of Helsinki, Helsinki 00290, Finland.

Macromolecular Crystallography Laboratory, National Cancer Institute, Basic Science Program, Leidos Biomedical Research Inc., Argonne, IL 60439, USA.

出版信息

J Mol Biol. 2020 Jun 12;432(13):3749-3760. doi: 10.1016/j.jmb.2020.04.005. Epub 2020 Apr 14.

DOI:10.1016/j.jmb.2020.04.005
PMID:32302608
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7306426/
Abstract

Optically controlled receptor tyrosine kinases (opto-RTKs) allow regulation of RTK signaling using light. Until recently, the majority of opto-RTKs were activated with blue-green light. Fusing a photosensory core module of Deinococcus radiodurans bacterial phytochrome (DrBphP-PCM) to the kinase domains of neurotrophin receptors resulted in opto-RTKs controlled with light above 650 nm. To expand this engineering approach to RTKs of other families, here we combined the DrBpP-PCM with the cytoplasmic domains of EGFR and FGFR1. The resultant Dr-EGFR and Dr-FGFR1 opto-RTKs are rapidly activated with near-infrared and inactivated with far-red light. The opto-RTKs efficiently trigger ERK1/2, PI3K/Akt, and PLCγ signaling. Absence of spectral crosstalk between the opto-RTKs and green fluorescent protein-based biosensors enables simultaneous Dr-FGFR1 activation and detection of calcium transients. Action mechanism of the DrBphP-PCM-based opto-RTKs is considered using the available RTK structures. DrBphP-PCM represents a versatile scaffold for engineering of opto-RTKs that are reversibly regulated with far-red and near-infrared light.

摘要

光控受体酪氨酸激酶(opto-RTKs)可利用光来调节 RTK 信号。直到最近,大多数 opto-RTKs 都是用蓝绿光激活的。将来自耐辐射球菌的细菌光敏色素(DrBphP-PCM)的光感核心模块与神经营养因子受体的激酶结构域融合,产生了可利用 650nm 以上光进行控制的 opto-RTKs。为了将这种工程方法扩展到其他家族的 RTKs,我们将 DrBpP-PCM 与 EGFR 和 FGFR1 的细胞质结构域结合。由此产生的 Dr-EGFR 和 Dr-FGFR1 opto-RTKs 可被近红外光快速激活,并被远红光失活。这些 opto-RTKs 能有效地触发 ERK1/2、PI3K/Akt 和 PLCγ 信号。opt-RTKs 和基于绿色荧光蛋白的生物传感器之间不存在光谱串扰,可实现 Dr-FGFR1 的同时激活和钙瞬变的检测。考虑到现有的 RTK 结构,我们认为 DrBphP-PCM 基 opto-RTKs 的作用机制是合理的。DrBphP-PCM 是一种多功能支架,可用于构建可被远红光和近红外光可逆调节的 opto-RTKs。