Construction of expression vectors and study on single-chain antibody and reshaping single-domain antibody against CD3
Two vectors, pWA180 and pROH80, for expression of single-chain Fv fragments (ScFv) were con-siruciea. (?)ne anti-CD3 VH and VL genes were amplified from UCHTl cells by RT-PCR and sequenced. Both genes were cloned in pWA180 to express native ScFv and pROH80 for GST-ScFv fusion protein expression. The...
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Published in: | Science China. Life sciences Vol. 40; no. 3; pp. 270 - 276 |
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Main Author: | |
Format: | Journal Article |
Language: | English |
Published: |
China
Springer Nature B.V
01-06-1997
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Subjects: | |
Online Access: | Get full text |
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Summary: | Two vectors, pWA180 and pROH80, for expression of single-chain Fv fragments (ScFv) were con-siruciea. (?)ne anti-CD3 VH and VL genes were amplified from UCHTl cells by RT-PCR and sequenced. Both genes were cloned in pWA180 to express native ScFv and pROH80 for GST-ScFv fusion protein expression. The expression products were analysed by ELISA and Western blot. The combining site of OKT3 was modeled. Human [g LS1 and Nd were selected as acceptors of CDRs of OKT3 VL and VH to construct a reshaping antibody against CD3. By com-paring OKT3, LS1 and Nd with their own family sequences, some residues were changed and the reshaping VL and VH genes were designed. The full VH gene was assembled in three steps with eight chemically synthesized oligonu-cleotide fragments using overlapping PCR and sequenced. The VH gene was expressed as active protein in pCOMB3 and as inclusion bodies in pGEX-4T-l by ELISA and Western blot analysis. |
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Bibliography: | LIU Xifu XIAO Sa , GU Zheng , WANG YongZHANG Weiguo , CHEN Ai , LIN QingHUANG Hualiang(Institute of Genetics, Chinese Academy of Sciences, Beijing 100101, China)SUN Jian CHEN Runsheng(Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China)SHEN Beifen and CHEN Xing(Institute of Basic Medicine, Academy of Military Medicine Sciences, Beijing 100850, China) 11-5841/Q ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1674-7305 1006-9305 1869-1889 1862-2798 |
DOI: | 10.1007/BF02879087 |