Ulrich H D, Driggers E M, Schultz P G
Howard Hughes Medical Institute, University of California, Berkeley 94720, USA.
Acta Chem Scand (Cph). 1996 Apr;50(4):328-32. doi: 10.3891/acta.chem.scand.50-0328.
In an effort to increase our insight into the catalysis of pericyclic reactions we have initiated a detailed study of an antibody that catalyzes an oxy-Cope rearrangement. We have determined the stereochemistry of the antibody-catalyzed reaction, and experiments are in progress to determine the conformation of the substrate bound in the antibody combining site. The genes encoding the variable regions of this antibody have been cloned and sequenced, and we have made use of a bacterial expression system to produce this antibody as a Fab fragment in recombinant form, making it amenable to genetic manipulations such as site-directed mutagenesis. The recombinant Fab fragment has been crystallized in the presence of its transition state analog, and we are now in the process of determining its active site structure.
为了更深入地了解周环反应的催化作用,我们启动了一项对催化氧杂-Cope重排反应的抗体的详细研究。我们已经确定了抗体催化反应的立体化学,并且正在进行实验以确定结合在抗体结合位点的底物的构象。编码该抗体可变区的基因已被克隆和测序,我们利用细菌表达系统以重组形式产生该抗体的Fab片段,使其适合进行诸如定点诱变等基因操作。重组Fab片段已在其过渡态类似物存在下结晶,我们目前正在确定其活性位点结构。