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FruitFire: a luciferase based on a fruit fly metabolic enzyme.
Adams, Spencer T; Zephyr, Jacqueto; Bohn, Markus F; Schiffer, Celia A; Miller, Stephen C.
Afiliação
  • Adams ST; Department of Biochemistry and Molecular Biotechnology, UMass Chan Medical School, 364 Plantation St, Worcester, MA 01605.
  • Zephyr J; Department of Biochemistry and Molecular Biotechnology, UMass Chan Medical School, 364 Plantation St, Worcester, MA 01605.
  • Bohn MF; Department of Biochemistry and Molecular Biotechnology, UMass Chan Medical School, 364 Plantation St, Worcester, MA 01605.
  • Schiffer CA; Department of Biochemistry and Molecular Biotechnology, UMass Chan Medical School, 364 Plantation St, Worcester, MA 01605.
  • Miller SC; Department of Biochemistry and Molecular Biotechnology, UMass Chan Medical School, 364 Plantation St, Worcester, MA 01605.
bioRxiv ; 2023 Jun 30.
Article em En | MEDLINE | ID: mdl-37425765
ABSTRACT
Firefly luciferase is homologous to fatty acyl-CoA synthetases from insects that are not bioluminescent. Here, we determined the crystal structure of the fruit fly fatty acyl-CoA synthetase CG6178 to 2.5 Å. Based on this structure, we mutated a steric protrusion in the active site to create the artificial luciferase FruitFire, which prefers the synthetic luciferin CycLuc2 to d-luciferin by >1000-fold. FruitFire enabled in vivo bioluminescence imaging in the brains of mice using the pro-luciferin CycLuc2-amide. The conversion of a fruit fly enzyme into a luciferase capable of in vivo imaging underscores the potential for bioluminescence with a range of adenylating enzymes from nonluminescent organisms, and the possibilities for application-focused design of enzyme-substrate pairs.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article