Hotta K, Lange H, Tantillo D J, Houk K N, Hilvert D, Wilson I A
Department of Molecular Biology and Skaggs Institute for Chemical Biology, The Scripps Research Institute, La Jolla, CA 92037, USA.
J Mol Biol. 2000 Oct 6;302(5):1213-25. doi: 10.1006/jmbi.2000.4503.
Antibody 21D8 catalyzes the solvent-sensitive decarboxylation of 3-carboxybenzisoxazoles. The crystal structure of chimeric Fab 21D8 with and without hapten at 1.61 A and 2.10 A, respectively, together with computational analysis, shows how a melange of polar and non-polar sites are exploited to achieve both substrate binding and acceleration of a reaction normally facilitated by purely aprotic dipolar media. The striking similarity of the decarboxylase and a series of unrelated esterase antibodies also highlights the chemical versatility of structurally conserved anion binding sites and the relatively subtle changes involved in fine-tuning the immunoglobulin pocket for recognition of different ligands and catalysis of different reactions.
抗体21D8催化3-羧基苯并异恶唑的溶剂敏感脱羧反应。分别在1.61 Å和2.10 Å分辨率下解析的结合和未结合半抗原的嵌合Fab 21D8晶体结构,结合计算分析表明,如何利用极性和非极性位点的混合来实现底物结合以及加速通常由纯非质子偶极介质促进的反应。脱羧酶与一系列不相关酯酶抗体的显著相似性也突出了结构保守的阴离子结合位点的化学多功能性,以及在微调免疫球蛋白口袋以识别不同配体和催化不同反应方面所涉及的相对细微的变化。