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      Selection and characterization of DARPins specific for the neurotensin receptor 1.

      Protein Engineering, Design and Selection
      Animals, Ankyrin Repeat, genetics, COS Cells, Cercopithecus aethiops, Chromatography, Gel, Enzyme-Linked Immunosorbent Assay, Epitope Mapping, Escherichia coli, Microscopy, Fluorescence, Peptide Library, Protein Binding, Protein Engineering, methods, Radioligand Assay, Rats, Receptors, Neurotensin, chemistry, metabolism, Recombinant Proteins, Substrate Specificity

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          Abstract

          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 microg 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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