Cargando…
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...
Autores principales: | , , , |
---|---|
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 |
_version_ | 1782363137919418368 |
---|---|
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. |
format | Online Article Text |
id | pubmed-4372190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT andersenkristena diazogroupsenduremetabolismandenablechemoselectivityincellulo AT aronoffmatthewr diazogroupsenduremetabolismandenablechemoselectivityincellulo AT mcgrathnicholasa diazogroupsenduremetabolismandenablechemoselectivityincellulo AT rainesronaldt diazogroupsenduremetabolismandenablechemoselectivityincellulo |