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A biocompatible "split luciferin" reaction and its application for non-invasive bioluminescent imaging of protease activity in living animals.
Godinat, Aurélien; Budin, Ghyslain; Morales, Alma R; Park, Hyo Min; Sanman, Laura E; Bogyo, Matthew; Yu, Allen; Stahl, Andreas; Dubikovskaya, Elena A.
Affiliation
  • Godinat A; Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology of Lausanne, Lausanne, Switzerland.
  • Budin G; Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology of Lausanne, Lausanne, Switzerland.
  • Morales AR; Institute of Chemical Sciences and Engineering, Swiss Federal Institute of Technology of Lausanne, Lausanne, Switzerland.
  • Park HM; Department of Nutritional Science and Toxicology, University of California Berkeley, Berkeley, California.
  • Sanman LE; Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, California.
  • Bogyo M; Department of Microbiology and Immunology, Stanford University School of Medicine, Stanford, California.
  • Yu A; Department of Pathology, Stanford University School of Medicine, Stanford, California.
  • Stahl A; Department of Nutritional Science and Toxicology, University of California Berkeley, Berkeley, California.
  • Dubikovskaya EA; Department of Nutritional Science and Toxicology, University of California Berkeley, Berkeley, California.
Curr Protoc Chem Biol ; 6(3): 169-189, 2014 Sep 09.
Article in En | MEDLINE | ID: mdl-25205565
ABSTRACT
The great complexity of many human pathologies, such as cancer, diabetes, and neurodegenerative diseases, requires new tools for studies of biological processes on the whole organism level. The discovery of novel biocompatible reactions has tremendously advanced our understanding of basic biology; however, no efficient tools exist for real-time non-invasive imaging of many human proteases that play very important roles in multiple human disorders. We recently reported that the "split luciferin" biocompatible reaction represents a valuable tool for evaluation of protease activity directly in living animals using bioluminescence imaging (BLI). Since BLI is the most sensitive in vivo imaging modality known to date, this method can be widely applied for the evaluation of the activity of multiple proteases, as well as identification of their new peptide-specific substrates. In this unit, we describe several applications of this "split luciferin" reaction for quantification of protease activities in test tube assays and living animals.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Hydrolases / Benzothiazoles / Molecular Imaging / Fluorescent Dyes Limits: Animals Language: En Journal: Curr Protoc Chem Biol Year: 2014 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Peptide Hydrolases / Benzothiazoles / Molecular Imaging / Fluorescent Dyes Limits: Animals Language: En Journal: Curr Protoc Chem Biol Year: 2014 Document type: Article Affiliation country:
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