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A Bacterial Phytochrome-based Optogenetic System Controllable with Near-infrared Light

Overview
Journal Nat Methods
Date 2016 May 10
PMID 27159085
Citations 105
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Abstract

Light-mediated control of protein-protein interactions to regulate cellular pathways is an important application of optogenetics. Here, we report an optogenetic system based on the reversible light-induced binding between the bacterial phytochrome BphP1 and its natural partner PpsR2 from Rhodopseudomonas palustris bacteria. We extensively characterized the BphP1-PpsR2 interaction both in vitro and in mammalian cells and then used this interaction to translocate target proteins to specific cellular compartments, such as the plasma membrane and the nucleus. We showed light-inducible control of cell morphology that resulted in a substantial increase of the cell area. We demonstrated light-dependent gene expression with 40-fold contrast in cultured cells, 32-fold in subcutaneous mouse tissue, and 5.7-fold in deep tissues in mice. Characteristics of the BphP1-PpsR2 optogenetic system include its sensitivity to 740- to 780-nm near-infrared light, its ability to utilize an endogenous biliverdin chromophore in eukaryotes (including mammals), and its spectral compatibility with blue-light-driven optogenetic systems.

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References
1.
Gasser C, Taiber S, Yeh C, Wittig C, Hegemann P, Ryu S . Engineering of a red-light-activated human cAMP/cGMP-specific phosphodiesterase. Proc Natl Acad Sci U S A. 2014; 111(24):8803-8. PMC: 4066486. DOI: 10.1073/pnas.1321600111. View

2.
Muller K, Engesser R, Metzger S, Schulz S, Kampf M, Busacker M . A red/far-red light-responsive bi-stable toggle switch to control gene expression in mammalian cells. Nucleic Acids Res. 2013; 41(7):e77. PMC: 3627562. DOI: 10.1093/nar/gkt002. View

3.
Gomez E, Gerhardt K, Judd J, Tabor J, Suh J . Light-Activated Nuclear Translocation of Adeno-Associated Virus Nanoparticles Using Phytochrome B for Enhanced, Tunable, and Spatially Programmable Gene Delivery. ACS Nano. 2015; 10(1):225-37. DOI: 10.1021/acsnano.5b05558. View

4.
Muller K, Engesser R, Timmer J, Nagy F, Zurbriggen M, Weber W . Synthesis of phycocyanobilin in mammalian cells. Chem Commun (Camb). 2013; 49(79):8970-2. DOI: 10.1039/c3cc45065a. View

5.
Kurokawa K, Itoh R, Yoshizaki H, Nakamura Y, Matsuda M . Coactivation of Rac1 and Cdc42 at lamellipodia and membrane ruffles induced by epidermal growth factor. Mol Biol Cell. 2003; 15(3):1003-10. PMC: 363057. DOI: 10.1091/mbc.e03-08-0609. View