A Programmable Signaling Molecular Recognition Nanocavity Prepared by Molecular Imprinting and Post-Imprinting Modifications
Inspired by biosystems, a process is proposed for preparing next‐generation artificial polymer receptors with molecular recognition abilities capable of programmable site‐directed modification following construction of nanocavities to provide multi‐functionality. The proposed strategy involves stric...
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Published in | Angewandte Chemie Vol. 128; no. 42; pp. 13217 - 13221 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English German |
Published |
Weinheim
Blackwell Publishing Ltd
10.10.2016
Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
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Summary: | Inspired by biosystems, a process is proposed for preparing next‐generation artificial polymer receptors with molecular recognition abilities capable of programmable site‐directed modification following construction of nanocavities to provide multi‐functionality. The proposed strategy involves strictly regulated multi‐step chemical modifications: 1) fabrication of scaffolds by molecular imprinting for use as molecular recognition fields possessing reactive sites for further modifications at pre‐determined positions, and 2) conjugation of appropriate functional groups with the reactive sites by post‐imprinting modifications to develop programmed functionalizations designed prior to polymerization, allowing independent introduction of multiple functional groups. The proposed strategy holds promise as a reliable, affordable, and versatile approach, facilitating the emergence of polymer‐based artificial antibodies bearing desirable functions that are beyond those of natural antibodies.
Nach dem Vorbild posttranslationaler Modifikationen in der Proteinbiosynthese wurden künstliche Polymerrezeptoren mit der Fähigkeit zur molekularen Erkennung entwickelt. Der Prozess umfasst die Herstellung reaktiver Zentren in Nanokavitäten, die eine programmierbare ortsgerichtete Multifunktionalisierung ermöglichen. |
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Bibliography: | istex:E7AF9C2FCBF07D71A0D0041687A6890156BE0E39 ark:/67375/WNG-F2023D5W-P ArticleID:ANGE201605992 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0044-8249 1521-3757 |
DOI: | 10.1002/ange.201605992 |