共 31 条
Selection and characterization of DARPins specific for the neurotensin receptor 1
被引:29
作者:

Milovnik, Peter
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机构:
Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland

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Sarkar, Casim A.
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机构:
Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland

Plueckthun, Andreas
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h-index: 0
机构:
Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland
机构:
[1] Univ Zurich, Inst Biochem, CH-8057 Zurich, Switzerland
基金:
美国国家卫生研究院;
关键词:
DARPins;
GPCR;
neurotensin;
NTR1;
ribosome display;
PROTEIN-COUPLED RECEPTOR;
ANKYRIN REPEAT PROTEINS;
IN-VITRO SELECTION;
CRYSTAL-STRUCTURE;
MEMBRANE-PROTEINS;
COMBINATORIAL LIBRARIES;
RIBOSOME DISPLAY;
PURIFICATION;
INHIBITION;
ANTAGONIST;
D O I:
10.1093/protein/gzp011
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
We describe here the selection and characterization of designed ankyrin repeat proteins (DARPins) that bind specifically to the rat neurotensin receptor 1 (NTR1), a G-protein coupled receptor (GPCR). The selection procedure using ribosome display and the initial clone analysis required < 10 mu g of detergent-solubilized, purified NTR1. Complex formation with solubilized GPCR was demonstrated by ELISA and size-exclusion chromatography; additionally, the GPCR could be detected in native membranes of mammalian cells using fluorescence microscopy. The main binding epitope in the GPCR lies within the 33 amino acids following the seventh transmembrane segment, which comprise the putative helix 8, and additional binding interactions are possibly contributed by the cytoplasmic loop 3, thus constituting a discontinuous epitope. Since the selected binders recognize the GPCR both in detergent-solubilized and in membrane-embedded forms, they will be potentially useful both in co-crystallization trials and for signal transduction experiments.
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页码:357 / 366
页数:10
相关论文
共 31 条
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