Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo
Author(s) -
Kristen A. Andersen,
Matthew R. Aronoff,
Nicholas A. McGrath,
Ronald T. Raines
Publication year - 2015
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja5095815
Subject(s) - diazo , chemoselectivity , chemistry , cycloaddition , metabolism , alkyne , derivative (finance) , functional group , 1,3 dipolar cycloaddition , stereochemistry , combinatorial chemistry , biochemistry , organic chemistry , catalysis , polymer , financial economics , economics
We introduce a stabilized diazo group as a reporter for chemical biology. ManDiaz, which is a diazo derivative of N-acetylmannosamine, is found to endure cellular metabolism and label the surface of a mammalian cell. There its diazo group can undergo a 1,3-dipolar cycloaddition with a strained alkyne, providing a signal comparable to that from the azido congener, ManNAz. The chemoselectivity of diazo and alkynyl groups enables dual labeling of cells that is not possible with azido and alkynyl groups. Thus, the diazo group, which is approximately half the size of an azido group, provides unique opportunities for orthogonal labeling of cellular components.
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