| Literature DB >> 35697806 |
Yuto Kuwasaki1, Kazushi Suzuki1, Gaigai Yu1, Shota Yamamoto1, Takahiro Otabe1, Yuki Kakihara1, Michiru Nishiwaki1, Keita Miyake2, Keiji Fushimi2, Ramsey Bekdash3,4, Yoshihiro Shimizu5, Rei Narikawa2,6, Takahiro Nakajima1,7, Masayuki Yazawa3,4, Moritoshi Sato8.
Abstract
Red light penetrates deep into mammalian tissues and has low phototoxicity, but few optogenetic tools that use red light have been developed. Here we present MagRed, a red light-activatable photoswitch that consists of a red light-absorbing bacterial phytochrome incorporating a mammalian endogenous chromophore, biliverdin and a photo-state-specific binder that we developed using Affibody library selection. Red light illumination triggers the binding of the two components of MagRed and the assembly of split-proteins fused to them. Using MagRed, we developed a red light-activatable Cre recombinase, which enables light-activatable DNA recombination deep in mammalian tissues. We also created red light-inducible transcriptional regulators based on CRISPR-Cas9 that enable an up to 378-fold activation (average, 135-fold induction) of multiple endogenous target genes. MagRed will facilitate optogenetic applications deep in mammalian organisms in a variety of biological research areas.Entities:
Year: 2022 PMID: 35697806 DOI: 10.1038/s41587-022-01351-w
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908