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利用配体-蛋白缀合物来监测配体-受体相互作用。

Exploiting ligand-protein conjugates to monitor ligand-receptor interactions.

机构信息

École Polytechnique Fédérale de Lausanne-EPFL, Institute of Chemical Sciences and Engineering, Institute of Bioengineering, National Centre of Competence in Research-NCCR in Chemical Biology, Lausanne, Switzerland.

出版信息

PLoS One. 2012;7(5):e37598. doi: 10.1371/journal.pone.0037598. Epub 2012 May 31.

Abstract

We introduce three assays for analyzing ligand-receptor interactions based on the specific conjugation of ligands to SNAP-tag fusion proteins. Conjugation of ligands to different SNAP-tag fusions permits the validation of suspected interactions in cell extracts and fixed cells as well as the establishment of high-throughput assays. The different assays allow the analysis of strong and weak interactions. Conversion of ligands into SNAP-tag substrates thus provides access to a powerful toolbox for the analysis of their interactions with proteins.

摘要

我们介绍了三种基于配体特异性连接到 SNAP 标签融合蛋白的配体-受体相互作用分析的测定方法。不同的 SNAP 标签融合物与配体的连接,允许在细胞提取物和固定细胞中验证可疑的相互作用,以及建立高通量测定方法。不同的测定方法可以分析强相互作用和弱相互作用。将配体转化为 SNAP 标签底物,因此为分析它们与蛋白质的相互作用提供了一个强大的工具箱。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6d7/3365113/3a13138b1b1f/pone.0037598.g001.jpg

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Time-resolved FRET between GPCR ligands reveals oligomers in native tissues.
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4
Selective cross-linking of interacting proteins using self-labeling tags.
J Am Chem Soc. 2009 Dec 16;131(49):17954-62. doi: 10.1021/ja907818q.
5
Review article: high-throughput affinity-based technologies for small-molecule drug discovery.
J Biomol Screen. 2009 Dec;14(10):1157-64. doi: 10.1177/1087057109350114.
6
Target profiling of small molecules by chemical proteomics.
Nat Chem Biol. 2009 Sep;5(9):616-24. doi: 10.1038/nchembio.216.
7
Semisynthetic fluorescent sensor proteins based on self-labeling protein tags.
J Am Chem Soc. 2009 Apr 29;131(16):5873-84. doi: 10.1021/ja900149e.
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An engineered protein tag for multiprotein labeling in living cells.
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