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Designing a Green Fluorogenic Protease Reporter by Flipping a Beta Strand of GFP for Imaging Apoptosis in Animals

  • Qiang Zhang
  • , Antonino Schepis
  • , Hai Huang
  • , Junjiao Yang
  • , Wen Ma
  • , Joaquim Torra
  • , Shao Qing Zhang
  • , Lina Yang
  • , Haifan Wu
  • , Santi Nonell
  • , Zhiqiang Dong
  • , Thomas B. Kornberg
  • , Shaun R. Coughlin
  • , Xiaokun Shu*
  • *Corresponding author for this work

Research output: Indexed journal article Articlepeer-review

77 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)4526-4530
Number of pages5
JournalJournal of the American Chemical Society
Volume141
Issue number11
DOIs
Publication statusPublished - 20 Mar 2019

Keywords

  • Programmed cell-death
  • Fluorescent protein
  • Caspase activation
  • Drosophila
  • Variants

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