Gibbs R A, Posner B A, Filpula D R, Dodd S W, Finkelman M A, Lee T K, Wroble M, Whitlow M, Benkovic S J
Department of Chemistry, Pennsylvania State University, University Park 16802.
Proc Natl Acad Sci U S A. 1991 May 1;88(9):4001-4. doi: 10.1073/pnas.88.9.4001.
The antigen-binding (Fab) fragment of the catalytic monoclonal antibody NPN43C9 has recently been cloned by using bacteriophage lambda. By inserting the variable regions of this Fab coding sequence into a (NH2)-VL-linker-VH-(COOH) construct (where VL and VH represent the heavy and light chain variable regions), we have assembled a recombinant gene encoding a catalytic single-chain antigen-binding protein. This protein has been expressed in Escherichia coli and exhibits the same catalytic parameters as the parent monoclonal antibody NPN43C9. Single-chain forms of catalytic antibodies may prove valuable for structural and site-directed mutagenesis studies as well as for large-scale applications of catalytic antibodies.
催化性单克隆抗体NPN43C9的抗原结合(Fab)片段最近已通过使用λ噬菌体进行克隆。通过将该Fab编码序列的可变区插入(NH2)-VL-连接子-VH-(COOH)构建体(其中VL和VH分别代表重链和轻链可变区),我们组装了一个编码催化性单链抗原结合蛋白的重组基因。该蛋白已在大肠杆菌中表达,并表现出与亲本单克隆抗体NPN43C9相同的催化参数。催化抗体的单链形式可能对结构和定点诱变研究以及催化抗体的大规模应用具有重要价值。