Literature DB >> 30710293

High Sensitive Quantitative Binding Assays Using a Nanoluciferase-Fused Probe for Analysis of ALG-2-Interacting Proteins.

Wei Zhang1, Rina Matsuo1, Terunao Takahara1, Hideki Shibata1, Masatoshi Maki2.   

Abstract

Many non-catalytic cellular proteins exert biological functions by formation of stable or transient complexes with other proteins. Analysis of the signal-induced physical interactions is important to understand their physiological roles in cells. Here we describe a biochemical method for assessing the binding of ALG-2 (gene name, PDCD6) to its target proteins that are immunoprecipitated from cell lysates. Application of nanoluciferase (Nluc)-fused ALG-2 enables a rapid quantitative evaluation of Ca2+-dependent interactions of target proteins with ALG-2 in vitro binding assays.

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Keywords:  ALG-2; Calcium-binding protein; EF-hand; In vitro binding; NanoLuc; Protein–protein interaction

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Year:  2019        PMID: 30710293     DOI: 10.1007/978-1-4939-9030-6_31

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  1 in total

1.  The Penta-EF-Hand ALG-2 Protein Interacts with the Cytosolic Domain of the SOCE Regulator SARAF and Interferes with Ubiquitination.

Authors:  Wei Zhang; Ayaka Muramatsu; Rina Matsuo; Naoki Teranishi; Yui Kahara; Terunao Takahara; Hideki Shibata; Masatoshi Maki
Journal:  Int J Mol Sci       Date:  2020-08-31       Impact factor: 5.923

  1 in total

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