Synthesis and properties of sulfhydryl-reactive near-infrared cyanine fluorochromes for fluorescence imaging.

TitleSynthesis and properties of sulfhydryl-reactive near-infrared cyanine fluorochromes for fluorescence imaging.
Publication TypeJournal Article
Year of Publication2003
AuthorsLin Y, Weissleder R, Tung C-H
JournalMol Imaging
Volume2
Issue2
Pagination87-92
Date Published2003 Apr
ISSN1535-3508
KeywordsCarbocyanines, Chromatography, High Pressure Liquid, Fluorescent Dyes, Iodoacetamide, Ligands, Microscopy, Fluorescence, Models, Chemical, Peptides, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Sulfhydryl Compounds, Sulfhydryl Reagents
Abstract

Near-infrared fluorochromes (NIRF) are useful compounds for diverse biotechnology applications and for in vivo biomedical imaging. Such NIRF must have high quantum yield, be biocompatible, and be conjugatable to a wide variety of proteins, peptides, and other affinity ligands. Here, we describe the synthesis of four new nonsymmetrical sulfhydryl-reactive cyanine NIRF with excellent optical and chemical properties. Each fluorochrome was designed to contain an iodoacetamido group that reacts specifically with sulfhydryl-containing molecules. The synthesized fluorochromes were used to label model peptides and sulfhydryl-containing biomolecules.

DOI10.1162/153535003322331975
Alternate JournalMol Imaging
PubMed ID12964306
Grant ListN01-CO17014 / CO / NCI NIH HHS / United States
P50-CA86355 / CA / NCI NIH HHS / United States
R33-CA88365 / 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