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
相关论文
共 36 条
[1]   Design of the linkers which effectively separate domains of a bifunctional fusion protein [J].
Arai, R ;
Ueda, H ;
Kitayama, A ;
Kamiya, N ;
Nagamune, T .
PROTEIN ENGINEERING, 2001, 14 (08) :529-532
[2]   Architecture and Membrane Interactions of the EGF Receptor [J].
Arkhipov, Anton ;
Shan, Yibing ;
Das, Rahul ;
Endres, Nicholas F. ;
Eastwood, Michael P. ;
Wemmer, David E. ;
Kuriyan, John ;
Shaw, David E. .
CELL, 2013, 152 (03) :557-569
[3]   Asymmetric tyrosine kinase arrangements in activation or autophosphorylation of receptor tyrosine kinases [J].
Bae, Jae Hyun ;
Schlessinger, Joseph .
MOLECULES AND CELLS, 2010, 29 (05) :443-448
[4]   The Selectivity of Receptor Tyrosine Kinase Signaling Is Controlled by a Secondary SH2 Domain Binding Site [J].
Bae, Jae Hyun ;
Lew, Erin Denise ;
Yuzawa, Satoru ;
Tome, Francisco ;
Lax, Irit ;
Schlessinger, Joseph .
CELL, 2009, 138 (03) :514-524
[5]   Structure of FGFR3 Transmembrane Domain Dimer: Implications for Signaling and Human Pathologies [J].
Bocharov, Eduard V. ;
Lesovoy, Dmitry M. ;
Goncharuk, Sergey A. ;
Goncharuk, Marina V. ;
Hristova, Kalina ;
Arseniev, Alexander S. .
STRUCTURE, 2013, 21 (11) :2087-2093
[6]  
Bocharov EV, 1858, BIOCHIM BIOPHYS ACTA, V2016, P1254
[7]   Light-inducible receptor tyrosine kinases that regulate neurotrophin signalling [J].
Chang, Ki-Young ;
Woo, Doyeon ;
Jung, Hyunjin ;
Lee, Sangkyu ;
Kim, Sungsoo ;
Won, Joungha ;
Kyung, Taeyoon ;
Park, Hyerim ;
Kim, Nury ;
Yang, Hee Won ;
Park, Jae-Yong ;
Hwang, Eun Mi ;
Kim, Daesoo ;
Do Heo, Won .
NATURE COMMUNICATIONS, 2014, 5
[8]   Ultrasensitive fluorescent proteins for imaging neuronal activity [J].
Chen, Tsai-Wen ;
Wardill, Trevor J. ;
Sun, Yi ;
Pulver, Stefan R. ;
Renninger, Sabine L. ;
Baohan, Amy ;
Schreiter, Eric R. ;
Kerr, Rex A. ;
Orger, Michael B. ;
Jayaraman, Vivek ;
Looger, Loren L. ;
Svoboda, Karel ;
Kim, Douglas S. .
NATURE, 2013, 499 (7458) :295-+
[9]   Near-Infrared Fluorescent Proteins, Biosensors, and Optogenetic Tools Engineered from Phytochromes [J].
Chernov, Konstantin G. ;
Redchuk, Taras A. ;
Omelina, Evgeniya S. ;
Verkhushaa, Vladislav V. .
CHEMICAL REVIEWS, 2017, 117 (09) :6423-6446
[10]   Phosphoinositide-specific phospholipase C in health and disease [J].
Cocco, Lucio ;
Follo, Matilde Y. ;
Manzoli, Lucia ;
Suh, Pann-Ghill .
JOURNAL OF LIPID RESEARCH, 2015, 56 (10) :1853-1860