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抗原结合受体的合成肽配体可诱导人B细胞淋巴瘤中的程序性细胞死亡。

Synthetic peptide ligands of the antigen binding receptor induce programmed cell death in a human B-cell lymphoma.

作者信息

Renschler M F, Bhatt R R, Dower W J, Levy R

机构信息

Division of Oncology, Stanford University Medical Center, CA 94305-5306.

出版信息

Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):3623-7. doi: 10.1073/pnas.91.9.3623.

Abstract

Peptide ligands for the antigen binding site of the surface immunoglobulin receptor of a human B-cell lymphoma cell line were identified with the use of filamentous phage libraries displaying random 8- and 12-amino acid peptides. Corresponding synthetic peptides bound specifically to the antigen binding site of this immunoglobulin receptor and blocked the binding of an anti-idiotype antibody. The ligands, when conjugated to form dimers or tetramers, induced cell death by apoptosis in vitro with an IC50 between 40 and 200 nM. This effect was associated with specific stimulation of intracellular protein tyrosine phosphorylation.

摘要

利用展示随机8氨基酸和12氨基酸肽的丝状噬菌体文库,鉴定出了人B细胞淋巴瘤细胞系表面免疫球蛋白受体抗原结合位点的肽配体。相应的合成肽特异性结合该免疫球蛋白受体的抗原结合位点,并阻断抗独特型抗体的结合。这些配体在缀合形成二聚体或四聚体时,在体外通过凋亡诱导细胞死亡,IC50在40至200 nM之间。这种效应与细胞内蛋白酪氨酸磷酸化的特异性刺激有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9493/43633/c1da65cde4ea/pnas01131-0158-a.jpg

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