| Literature DB >> 2024120 |
P Wirsching1, J A Ashley, S J Benkovic, K D Janda, R A Lerner.
Abstract
A transition state analogue was used to produce a mouse antibody that catalyzes transesterification in water. The antibody behaves as a highly efficient catalyst with a covalent intermediate and the characteristic of induced fit. While some features of the catalytic pathway were programmed when the hapten was designed and reflect favorable substrate-antibody interactions, other features are a manifestation of the chemical potential of antibody diversity. The fact that antibodies recapitulate mechanisms and pathways previously thought to be a characteristic of highly evolved enzymes suggests that once an appropriate binding cavity is achieved, reaction pathways commensurate with the intrinsic chemical potential of proteins ensue.Entities:
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Year: 1991 PMID: 2024120 DOI: 10.1126/science.2024120
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728