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Summary
February 2008, Vol. 5, No. 2, Pages 149-153
, DOI 10.1517/17425247.5.2.149
Applications of glycosyltransferases in the site-specific conjugation of biomolecules and the development of a targeted drug delivery system and contrast agents for MRIBoopathy Ramakrishnan 1,2, Elizabeth Boeggeman 1,2 & Pradman K Qasba †31NCI-Frederick, Center for Cancer Research, Center for Cancer Research Nanobiology Program, Structural Glycobiology Section, Building 469, Room 221, Frederick, MD 21702, USA 2NCI-Frederick, Center for Cancer Research, Center for Cancer Research Nanobiology Program, SAIC-Frederick, Inc., Basic Research Program, Frederick, MD 21702, USA 3NCI-Frederick, Center for Cancer Research, Center for Cancer Research Nanobiology Program, Structural Glycobiology Section, Building 469, Room 221, Frederick, MD 21702, USA +1 301 846 1934; +1 301 846 7149; qasba@helix.nih.gov † Author for correspondence Background: The delivery of drugs to the proposed site of action is a challenging task. Tissue and cell-specific guiding molecules are being used to carry a cargo of therapeutic molecules. The cargo molecules need to be conjugated in a site-specific manner to the therapeutic molecules such that the bioefficacy of these molecules is not compromised. Methods: Using wild-type and mutant glycosyltransferases, the sugar moiety with a unique chemical handle is incorporated at a specific site in the cargo or therapeutic molecules, making it possible to conjugate these molecules through the chemical handle present on the modified glycan. Results/conclusions: The modified glycan residues introduced at specific sites on the cargo molecule make it possible to conjugate fluorophores for ELISA-based assays, radionuclides for imaging and immunotherapy applications, lipids for the assembly of immunoliposomes, cytotoxic drugs, cytokines, or toxins for antibody-based cancer therapy and the development of a targeted drug delivery system.
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