A self-immolative reporter for beta-galactosidase sensing.

TitleA self-immolative reporter for beta-galactosidase sensing.
Publication TypeJournal Article
Year of Publication2007
AuthorsHo N-H, Weissleder R, Tung C-H
JournalChembiochem
Volume8
Issue5
Pagination560-6
Date Published2007 Mar 26
ISSN1439-4227
Keywordsbeta-Galactosidase, beta-Glucosidase, Carbohydrates, Enzymes, Galactose, Galactosides, Glucuronidase, Glycine, Hydrogen-Ion Concentration, Hydrolysis, Kinetics, Microscopy, Fluorescence, Models, Chemical, Time Factors, Water
Abstract

A dual fluorogenic and chromogenic probe, Gal-2SBPO, has been developed based on a synthesized water-soluble dye, 9-di-3-sulfonyl-propylaminobenzo[a]phenoxazonium perchloride (2SPBO, lambda(ex/em)=630/670 nm). beta-D-Galactopyranoside, the substrate of beta-galactosidase, was conjugated to 2SBPO through a para-substituted benzyloxycarbonyl group and a glycine residue, which serve as a self-immolative spacer and as a molecular blocker to mask the optical signal of 2SBPO, respectively. Gal-2SBPO was soluble and stable under physiological conditions. Enzymatic cleavage of the beta-D-galactopyranoside triggered a series of spontaneous reactions that resulted in a release of optically active 2SBPO. The beta-galactosidase activity was assayed by monitoring the absorbance at 630 nm and fluorescence at 670 nm.

DOI10.1002/cbic.200600386
Alternate JournalChembiochem
PubMed ID17300128
Grant ListP50 CA 86355 / CA / NCI NIH HHS / United States
R01 CA 99385 / CA / NCI NIH HHS / United States
Related Institute: 
Molecular Imaging Innovations Institute (MI3)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065