| Literature DB >> 30821975 |
Qiang Zhang1,2, Antonino Schepis2, Hai Huang2, Junjiao Yang1,2, Wen Ma3, Joaquim Torra1,2,4, Shao-Qing Zhang5, Lina Yang6, Haifan Wu1,2, Santi Nonell4, Zhiqiang Dong6, Thomas B Kornberg2, Shaun R Coughlin2, Xiaokun Shu1,2.
Abstract
A family of proteases called caspases mediate apoptosis signaling in animals. We report a GFP-based fluorogenic protease reporter, dubbed "FlipGFP", by flipping a beta strand of the GFP. Upon protease activation and cleavage, the beta strand is restored, leading to reconstitution of the GFP and fluorescence. FlipGFP-based TEV protease reporter achieves 100-fold fluorescence change. A FlipGFP-based executioner caspase reporter visualized apoptosis in live zebrafish embryos with spatiotemporal resolution. FlipGFP also visualized apoptotic cells in the midgut of Drosophila. Thus, the FlipGFP-based caspase reporter will be useful for monitoring apoptosis during animal development and for designing reporters of proteases beyond caspases. The design strategy can be further applied to a red fluorescent protein for engineering a red fluorogenic protease reporter.Entities:
Year: 2019 PMID: 30821975 PMCID: PMC6486793 DOI: 10.1021/jacs.8b13042
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419