Development of Copper-Catalyzed Azide-Alkyne Cycloaddition for Increased in Vivo Efficacy of Interferon [Beta]-1b by Site-Specific PEGylation
The development of protein conjugate therapeutics requires control over the site of modification to allow for reproducible generation of a product with the desired potency, pharmacokinetic, and safety profile. Placement of a single nonnatural amino acid at the desired modification site of a recombin...
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Published in | Bioconjugate chemistry Vol. 23; no. 10; p. 2087 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Washington
American Chemical Society
17.10.2012
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Subjects | |
Online Access | Get full text |
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