Developing fluorescence sensor probe to capture activated muscle-specific calpain-3 (CAPN3) in living muscle cells

Biol Open. 2020 Sep 4;9(9):bio048975. doi: 10.1242/bio.048975.

Abstract

Calpain-3 (CAPN3) is a muscle-specific type of calpain whose protease activity is triggered by Ca2+ Here, we developed CAPN3 sensor probes (SPs) to detect activated-CAPN3 using a fluorescence/Förster resonance energy transfer (FRET) technique. In our SPs, partial amino acid sequence of calpastatin, endogenous CAPN inhibitor but CAPN3 substrate, is inserted between two different fluorescence proteins that cause FRET. Biochemical and spectral studies revealed that CAPN3 cleaved SPs and changed emission wavelengths of SPs. Importantly, SPs were scarcely cleaved by CAPN1 and CAPN2. Furthermore, our SP successfully captured the activation of endogenous CAPN3 in living myotubes treated with ouabain. Our SPs would become a promising tool to detect the dynamics of CAPN3 protease activity in living cells.

Keywords: Calpain; Calpain-3; Calpainopathy; Limb-girdle muscular dystrophy type 2A; Proteolysis; Skeletal muscle.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biosensing Techniques / methods*
  • Calpain / genetics
  • Calpain / metabolism*
  • Fluorescence Resonance Energy Transfer
  • Fluorescence*
  • Fluorescent Dyes*
  • Gene Expression
  • Humans
  • Mice
  • Molecular Imaging / methods*
  • Muscle Cells / metabolism*
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*

Substances

  • Fluorescent Dyes
  • Muscle Proteins
  • Calpain
  • Capn3 protein, mouse