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Generation of Dynamic Combinatorial Libraries Using Hydrazone‐Functionalized Surface Mimetics

Dynamic combinatorial chemistry (DCC) represents an approach, whereby traditional supramolecular scaffolds used for protein surface recognition might be exploited to achieve selective high affinity target recognition. Synthesis, in situ screening and amplification under selection pressure allows the...

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Detalles Bibliográficos
Autores principales: Hewitt, Sarah H., Wilson, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947633/
https://www.ncbi.nlm.nih.gov/pubmed/29780280
http://dx.doi.org/10.1002/ejoc.201800022
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author Hewitt, Sarah H.
Wilson, Andrew J.
author_facet Hewitt, Sarah H.
Wilson, Andrew J.
author_sort Hewitt, Sarah H.
collection PubMed
description Dynamic combinatorial chemistry (DCC) represents an approach, whereby traditional supramolecular scaffolds used for protein surface recognition might be exploited to achieve selective high affinity target recognition. Synthesis, in situ screening and amplification under selection pressure allows the generation of ligands, which bear different moieties capable of making multivalent non‐covalent interactions with target proteins. Generic tetracarboxyphenyl porphyrin scaffolds bearing four hydrazide moieties have been used to form dynamic combinatorial libraries (DCLs) using aniline‐catalyzed reversible hydrazone exchange reactions, in 10 % DMSO, 5 mm NH(4)OAc, at pH 6.75. High resolution mass spectrometry (HRMS) was used to monitor library composition and establish conditions under which equilibria were established.
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spelling pubmed-59476332018-05-17 Generation of Dynamic Combinatorial Libraries Using Hydrazone‐Functionalized Surface Mimetics Hewitt, Sarah H. Wilson, Andrew J. European J Org Chem Full Papers Dynamic combinatorial chemistry (DCC) represents an approach, whereby traditional supramolecular scaffolds used for protein surface recognition might be exploited to achieve selective high affinity target recognition. Synthesis, in situ screening and amplification under selection pressure allows the generation of ligands, which bear different moieties capable of making multivalent non‐covalent interactions with target proteins. Generic tetracarboxyphenyl porphyrin scaffolds bearing four hydrazide moieties have been used to form dynamic combinatorial libraries (DCLs) using aniline‐catalyzed reversible hydrazone exchange reactions, in 10 % DMSO, 5 mm NH(4)OAc, at pH 6.75. High resolution mass spectrometry (HRMS) was used to monitor library composition and establish conditions under which equilibria were established. John Wiley and Sons Inc. 2018-04-25 2018-04-30 /pmc/articles/PMC5947633/ /pubmed/29780280 http://dx.doi.org/10.1002/ejoc.201800022 Text en © 2018 The Authors. Published by Wiley‐VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Full Papers
Hewitt, Sarah H.
Wilson, Andrew J.
Generation of Dynamic Combinatorial Libraries Using Hydrazone‐Functionalized Surface Mimetics
title Generation of Dynamic Combinatorial Libraries Using Hydrazone‐Functionalized Surface Mimetics
title_full Generation of Dynamic Combinatorial Libraries Using Hydrazone‐Functionalized Surface Mimetics
title_fullStr Generation of Dynamic Combinatorial Libraries Using Hydrazone‐Functionalized Surface Mimetics
title_full_unstemmed Generation of Dynamic Combinatorial Libraries Using Hydrazone‐Functionalized Surface Mimetics
title_short Generation of Dynamic Combinatorial Libraries Using Hydrazone‐Functionalized Surface Mimetics
title_sort generation of dynamic combinatorial libraries using hydrazone‐functionalized surface mimetics
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947633/
https://www.ncbi.nlm.nih.gov/pubmed/29780280
http://dx.doi.org/10.1002/ejoc.201800022
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