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

被引:16
|
作者
Leopold, Anna, V [1 ]
Pletnev, Sergei [2 ]
Verkhusha, Vladislav V. [1 ,3 ,4 ]
机构
[1] Univ Helsinki, Fac Med, Med, Helsinki 00290, Finland
[2] Leidos Biomed Res Inc, Macromol Crystallog Lab, NCI, Basic Sci Program, Argonne, IL 60439 USA
[3] Albert Einstein Coll Med, Dept Anat & Struct Biol, Bronx, NY 10461 USA
[4] Albert Einstein Coll Med, Gruss Lipper Biophoton Ctr, Bronx, NY 10461 USA
基金
美国国家卫生研究院; 芬兰科学院;
关键词
bacteriophytochrome; DrBphP; EGFR; FGFR1; opto-RTK; FLUORESCENT PROTEINS; ACTIVATION; DOMAIN; BIOSENSORS; MEMBRANE;
D O I
10.1016/j.jmb.2020.04.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 PLC gamma 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. (C) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3749 / 3760
页数:12
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