| Literature DB >> 26808669 |
Jianjun He1, Yi Wang2, Maria A Missinato3, Ezenwa Onuoha3, Lydia A Perkins2, Simon C Watkins4, Claudette M St Croix4, Michael Tsang3, Marcel P Bruchez1,2,5.
Abstract
Upon illumination, photosensitizer molecules produce reactive oxygen species that can be used for functional manipulation of living cells, including protein inactivation, targeted-damage introduction and cellular ablation. Photosensitizers used to date have been either exogenous, resulting in delivery and removal challenges, or genetically encoded proteins that form or bind a native photosensitizing molecule, resulting in a constitutively active photosensitizer inside the cell. We describe a genetically encoded fluorogen-activating protein (FAP) that binds a heavy atom-substituted fluorogenic dye, forming an 'on-demand' activated photosensitizer that produces singlet oxygen and fluorescence when activated with near-infrared light. This targeted and activated photosensitizer (TAPs) approach enables protein inactivation, targeted cell killing and rapid targeted lineage ablation in living larval and adult zebrafish. The near-infrared excitation and emission of this FAP-TAPs provides a new spectral range for photosensitizer proteins that could be useful for imaging, manipulation and cellular ablation deep within living organisms.Entities:
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Year: 2016 PMID: 26808669 PMCID: PMC4916159 DOI: 10.1038/nmeth.3735
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547