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作 者:孙键[1] 沈如群[1] 徐琳[1] 陈润生[1] 刘喜富[1] 黄华梁[1]
机构地区:[1]中科院生物物理所,中科院遗传所
出 处:《生物物理学报》1996年第1期119-124,共6页Acta Biophysica Sinica
摘 要:使用同源建模的方法通过计算机模拟鼠抗体OKT3抗原结合位点的空间结构,在结构分析及人和鼠抗体各自保守序列分析的基础上,设计出抗CD3的改形抗体序列;并进一步模拟改形抗体的结构,理论计算和实验的结果表明改形设计是合理的。In order to construct reshaping anti-CD3 antibody, the combining sites of OKT3 weremodeled using the knowledge-based method. On the basis of homology of sequence, humanIg LS1 and ND were selected as acceptors for CDRs of OKT3 VL and VH. By analyzing thetertiary structure of OKT3 and comparing the primary sequence of OKT3, LS1 and ND withtheir own family sequences, some residues in the framework regions were changed and thereshaped VL and VH genes were designed. Also the structural differennces between the originalOKT3 and the reshaped antibody were analyzed. In primary experiment the ashaped antibodyshowed competitive inhibition activities against OKT3 by ELISA.
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