Programing Chemical Communication: Allostery vs Multivalent Mechanism
Author:
Affiliation:
1. Département de Chimie, Laboratoire de Biosenseurs et Nanomachines, Université de Montréal, Montréal QC H2V 0B3, Canada
Funder
Canada Research Chairs
Natural Sciences and Engineering Research Council of Canada
Fonds de recherche du Qu?bec - Nature et technologies
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.3c04045
Reference58 articles.
1. Understanding biophysicochemical interactions at the nano–bio interface
2. The ensemble nature of allostery
3. Rational Design of Allosteric Inhibitors and Activators Using the Population-Shift Model: In Vitro Validation and Application to an Artificial Biosensor
4. Using the Population-Shift Mechanism to Rationally Introduce “Hill-type” Cooperativity into a Normally Non-Cooperative Receptor
5. Intrinsic disorder as a generalizable strategy for the rational design of highly responsive, allosterically cooperative receptors
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