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Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo

[Image: see text] 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 wit...

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Autores principales: Andersen, Kristen A., Aronoff, Matthew R., McGrath, Nicholas A., Raines, Ronald T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372190/
https://www.ncbi.nlm.nih.gov/pubmed/25658416
http://dx.doi.org/10.1021/ja5095815
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author Andersen, Kristen A.
Aronoff, Matthew R.
McGrath, Nicholas A.
Raines, Ronald T.
author_facet Andersen, Kristen A.
Aronoff, Matthew R.
McGrath, Nicholas A.
Raines, Ronald T.
author_sort Andersen, Kristen A.
collection PubMed
description [Image: see text] 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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spelling pubmed-43721902015-03-24 Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo Andersen, Kristen A. Aronoff, Matthew R. McGrath, Nicholas A. Raines, Ronald T. J Am Chem Soc [Image: see text] 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. American Chemical Society 2015-02-06 2015-02-25 /pmc/articles/PMC4372190/ /pubmed/25658416 http://dx.doi.org/10.1021/ja5095815 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Andersen, Kristen A.
Aronoff, Matthew R.
McGrath, Nicholas A.
Raines, Ronald T.
Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo
title Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo
title_full Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo
title_fullStr Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo
title_full_unstemmed Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo
title_short Diazo Groups Endure Metabolism and Enable Chemoselectivity in Cellulo
title_sort diazo groups endure metabolism and enable chemoselectivity in cellulo
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4372190/
https://www.ncbi.nlm.nih.gov/pubmed/25658416
http://dx.doi.org/10.1021/ja5095815
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