共 30 条
Making artificial antibodies: A format for phage display of combinatorial heterodimeric arrays
被引:109
作者:

Gao, CS
论文数: 0 引用数: 0
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机构: Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA

Mao, SL
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机构: Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA

Lo, CHL
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h-index: 0
机构: Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA

Wirsching, P
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h-index: 0
机构: Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA

Lerner, RA
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机构: Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA

Janda, KD
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机构: Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
机构:
[1] Scripps Res Inst, Dept Chem, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Mol Biol, La Jolla, CA 92037 USA
[3] Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
来源:
关键词:
D O I:
10.1073/pnas.96.11.6025
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
The gene MI protein (pVII) and gene IX protein (pIX) are associated closely on the surface of filamentous bacteriophage that is opposite of the end harboring the widely exploited pIII protein. We developed a phagemid format wherein antibody heavy- and light-chain variable regions were fused to the amino termini of pVII and pIX, respectively. Significantly, the fusion proteins interacted to form a functional Fv-binding domain on the phage surface. Our approach will be applicable to the display of generic peptide and protein libraries that can form combinatorial heterodimeric arrays. Consequently, it represents a first step toward artificial antibodies and the selection of novel biological activities.
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页码:6025 / 6030
页数:6
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