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On-Demand Targeting: Investigating Biology with Proximity-Directed Chemistry

[Image: see text] Proximity enhancement is a central chemical tenet underpinning an exciting suite of small-molecule toolsets that have allowed us to unravel many biological complexities. The leitmotif of this opus is “tethering”—a strategy in which a multifunctional small molecule serves as a templ...

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Autores principales: Long, Marcus J. C., Poganik, Jesse R., Aye, Yimon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805449/
https://www.ncbi.nlm.nih.gov/pubmed/26907082
http://dx.doi.org/10.1021/jacs.5b12608
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author Long, Marcus J. C.
Poganik, Jesse R.
Aye, Yimon
author_facet Long, Marcus J. C.
Poganik, Jesse R.
Aye, Yimon
author_sort Long, Marcus J. C.
collection PubMed
description [Image: see text] Proximity enhancement is a central chemical tenet underpinning an exciting suite of small-molecule toolsets that have allowed us to unravel many biological complexities. The leitmotif of this opus is “tethering”—a strategy in which a multifunctional small molecule serves as a template to bring proteins/biomolecules together. Scaffolding approaches have been powerfully applied to control diverse biological outcomes such as protein–protein association, protein stability, activity, and improve imaging capabilities. A new twist on this strategy has recently appeared, in which the small-molecule probe is engineered to unleash controlled amounts of reactive chemical signals within the microenvironment of a target protein. Modification of a specific target elicits a precisely timed and spatially controlled gain-of-function (or dominant loss-of-function) signaling response. Presented herein is a unique personal outlook conceptualizing the powerful proximity-enhanced chemical biology toolsets into two paradigms: “multifunctional scaffolding” versus “on-demand targeting”. By addressing the latest advances and challenges in the established yet constantly evolving multifunctional scaffolding strategies as well as in the emerging on-demand precision targeting (and related) systems, this Perspective is aimed at choosing when it is best to employ each of the two strategies, with an emphasis toward further promoting novel applications and discoveries stemming from these innovative chemical biology platforms.
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spelling pubmed-48054492016-03-23 On-Demand Targeting: Investigating Biology with Proximity-Directed Chemistry Long, Marcus J. C. Poganik, Jesse R. Aye, Yimon J Am Chem Soc [Image: see text] Proximity enhancement is a central chemical tenet underpinning an exciting suite of small-molecule toolsets that have allowed us to unravel many biological complexities. The leitmotif of this opus is “tethering”—a strategy in which a multifunctional small molecule serves as a template to bring proteins/biomolecules together. Scaffolding approaches have been powerfully applied to control diverse biological outcomes such as protein–protein association, protein stability, activity, and improve imaging capabilities. A new twist on this strategy has recently appeared, in which the small-molecule probe is engineered to unleash controlled amounts of reactive chemical signals within the microenvironment of a target protein. Modification of a specific target elicits a precisely timed and spatially controlled gain-of-function (or dominant loss-of-function) signaling response. Presented herein is a unique personal outlook conceptualizing the powerful proximity-enhanced chemical biology toolsets into two paradigms: “multifunctional scaffolding” versus “on-demand targeting”. By addressing the latest advances and challenges in the established yet constantly evolving multifunctional scaffolding strategies as well as in the emerging on-demand precision targeting (and related) systems, this Perspective is aimed at choosing when it is best to employ each of the two strategies, with an emphasis toward further promoting novel applications and discoveries stemming from these innovative chemical biology platforms. American Chemical Society 2016-02-23 2016-03-23 /pmc/articles/PMC4805449/ /pubmed/26907082 http://dx.doi.org/10.1021/jacs.5b12608 Text en Copyright © 2016 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 Long, Marcus J. C.
Poganik, Jesse R.
Aye, Yimon
On-Demand Targeting: Investigating Biology with Proximity-Directed Chemistry
title On-Demand Targeting: Investigating Biology with Proximity-Directed Chemistry
title_full On-Demand Targeting: Investigating Biology with Proximity-Directed Chemistry
title_fullStr On-Demand Targeting: Investigating Biology with Proximity-Directed Chemistry
title_full_unstemmed On-Demand Targeting: Investigating Biology with Proximity-Directed Chemistry
title_short On-Demand Targeting: Investigating Biology with Proximity-Directed Chemistry
title_sort on-demand targeting: investigating biology with proximity-directed chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4805449/
https://www.ncbi.nlm.nih.gov/pubmed/26907082
http://dx.doi.org/10.1021/jacs.5b12608
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