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Chemoselective Modification of Viral Surfaces via Bioorthogonal Click Chemistry
Published on: August 19, 2012
Efficient Synthetic Approach to Linear Dasatinib-DNA Conjugates by Click Chemistry
Nan-Sheng Li1,2, Nathan P Gossai1,2, Jordan A Naumann1,2
1Department of Biochemistry & Molecular Biology and ‡Department of Chemistry, University of Chicago , 929 East 57th Street, Chicago, Illinois 60637, United States.
Abstract:
A pair of synthetic approaches to linear dasatinib-DNA conjugates via click chemistry are described. The first approach involves the reaction of excess azido dasatinib derivative with 5'-(5-hexynyl)-tagged DNAs, and the second involves the reaction of excess alkynyl-linked dasatinib with 5'-azido-tagged DNA. The second approach using alkynyl-derived dasatinib and 5'-azido-tagged DNA yielded the corresponding dasatinib-DNA conjugates in higher yield (47% versus 10-33% for the first approach). Studies have shown these linear dasatinib-DNA conjugates-derived gold nanoparticles exhibit efficacy against leukemia cancer cells with reduced toxicity toward normal cells compared to that of free dasatinib.

