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DESIGN OF ANTI-CD3 ScFv-B7.1 FUSION MOLECULE AND PREDICTION OF ITS BIOLOGICAL CHARACTERISTICS
作者姓名:杨章民  司履生  王一理  来宝长
作者单位:Institute for Cancer Research,School of Life Science & Technology,Institute for Cancer Research,School of Life Science & Technology,Institute for Cancer Research,School of Life Science & Technology,Institute for Cancer Research,School of Life Science & Technology Xi'an Jiaotong University,Xi'an 710061,China,Xi'an Jiaotong University,Xi'an 710061,China,Xi'an Jiaotong University,Xi'an 710061,China,Xi'an Jiaotong University,Xi'an 710061,China
基金项目:ThisworkwassupportedbytheScientificResearchFoundationofHealthMinistryofChina(No .98 1 2 32 )
摘    要:Geneticallyengineeredbifunctional proteinshaveshown promising prospectsintumorclinicaladministrationandbasicresearch .Anti CD3ScFv(anti CD3Single chainfragmentofvariablere gion)isakindofrecombinantengineeredantibodyderivedfrommurineOKT3hybridoma .Asapotentmi…


DESIGN OF ANTI-CD3 ScFv-B7.1 FUSION MOLECULE AND PREDICTION OF ITS BIOLOGICAL CHARACTERISTICS
Institution:Institute for Cancer Research, School of Life Science & Technology, Xi'an Jiaotong University, Xi'an 710061,China.
Abstract:Objective To design and construct the eukaryotic expression vector which expresses Anti-CD3 ScFv-B7.1 fusion molecules and predict the biological characteristics, the rationality and feasibility of the spacer. Methods To analyze the flexibility, Hoop & Woods hydrophilicity and the epitope of Anti-CD3 ScFv-B7.1 fusion molecule at secondary structure level by computer simulation utilizing the GoldKey software. Results By comparing with Anti-CD3 ScFv and B7.1 respectively, it shows that Anti-CD3 ScFv-B7.1 fusion molecules can form correct secondary structure with the linking of the spacer, the fusion does not change the original hydrophilicity and epitopes of both Anti-CD3 ScFv and B7.1, no new epitopes emerge; The spacer is flexible and shows low antigenicity. Conclusion The design of Anti-CD3 ScFv-B7.1 fusion molecule are rational and feasible, the expressed fusion protein could retain the maximum biological activity and the function of both Anti-CD3 ScFv and B7.1.
Keywords:anti-CD3 ScFv  B7  1  fusion gene  computer simulation
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