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催化抗体与萜烯环化酶机制的融合:由碳正离子-π相互作用引导的多烯环化反应

Convergence of Catalytic Antibody and Terpene Cyclase Mechanisms: Polyene Cyclization Directed by Carbocation-π Interactions.

作者信息

Paschall Chiana M, Hasserodt Jens, Jones Terri, Lerner Richard A, Janda Kim D, Christianson David W

机构信息

Roy and Diana Vagelos Laboratories, Department of Chemistry, University of Pennsylvania, Philadelphia, PA 19104-6323 (USA), Fax: (+1) 215-573-2201.

Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, CA 92037 (USA).

出版信息

Angew Chem Int Ed Engl. 1999 Jun 14;38(12):1743-1747. doi: 10.1002/(SICI)1521-3773(19990614)38:12<1743::AID-ANIE1743>3.0.CO;2-3.

Abstract

A tandem cationic cyclization cascade similar to a terpenoid cyclase reaction is catalyzed by antibody HA5-19A4. The 2.7-Å resolution crystal structure of the Fab-hapten complex reveals convergence with the same catalytic strategy employed by a terpenoid cyclase: both serve as templates that enforce the productive conformation of a flexible polyene substrate, and both stabilize carbocation intermediates through cation-π interactions with multiple aromatic residues in their active sites.

摘要

抗体HA5-19A4催化一种类似于萜类环化酶反应的串联阳离子环化级联反应。Fab-半抗原复合物的2.7埃分辨率晶体结构揭示了其与萜类环化酶所采用的相同催化策略的趋同:两者都作为模板来强制柔性多烯底物形成有效构象,并且都通过与活性位点中多个芳香族残基的阳离子-π相互作用来稳定碳正离子中间体。

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