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一种抗人CD34小鼠单克隆抗体的从头蛋白质测序、人源化及体外效应

De novo protein sequencing, humanization and in vitro effects of an antihuman CD34 mouse monoclonal antibody.

作者信息

Fan Chia-Yu, Huang Sheng-Yu, Chou Min-Yuan, Lyu Ping-Chiang

机构信息

Institute of Bioinformatics and Structural Biology & Department of Life Science, National Tsing Hua University, Hsinchu, Taiwan.

Biomedical Technology and Device Research Laboratories, Industrial Technology Research Institute, Hsinchu, Taiwan.

出版信息

Biochem Biophys Rep. 2016 Nov 18;9:51-60. doi: 10.1016/j.bbrep.2016.11.006. eCollection 2017 Mar.

Abstract

QBEND/10 is a mouse immunoglobulin lambda-chain monoclonal antibody with strict specificity against human hematopoietic progenitor cell antigen CD34. Our in vitro study showed that QBEND/10 impairs the tube formation of human umbilical vein endothelial cells (HUVECs), suggesting that the antibody may be of potential benefit in blocking tumor angiogenesis. We provided a de novo protein sequencing method through tandem mass spectrometry to identify the amino acid sequences in the variable heavy and light chains of QBEND/10. To reduce immunogenicity for clinical applications, QBEND/10 was further humanized using the resurfacing approach. We demonstrate that the de novo sequenced and humanized QBEND/10 retains the biological functions of the parental mouse counterpart, including the binding kinetics to CD34 and blockage of the tube formation of the HUVECs.

摘要

QBEND/10是一种小鼠免疫球蛋白λ链单克隆抗体,对人类造血祖细胞抗原CD34具有严格的特异性。我们的体外研究表明,QBEND/10会损害人脐静脉内皮细胞(HUVECs)的管腔形成,这表明该抗体在阻断肿瘤血管生成方面可能具有潜在益处。我们提供了一种通过串联质谱进行从头蛋白质测序的方法,以鉴定QBEND/10重链和轻链可变区中的氨基酸序列。为了降低临床应用中的免疫原性,我们使用表面重塑方法对QBEND/10进行了进一步人源化。我们证明,从头测序和人源化后的QBEND/10保留了亲本小鼠抗体的生物学功能,包括与CD34的结合动力学以及对HUVECs管腔形成的阻断作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67d8/5614552/d7b87be19ecf/gr1.jpg

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