Literature DB >> 34014520

A Fluorescence-Based Assay to Determine PDZ-Ligand Binding Thermodynamics.

Young Joo Sun1, Ernesto J Fuentes2,3.   

Abstract

Postsynaptic density-95, disks-large, and zonula occludens-1 (PDZ) domain interactions with cognate linear binding motifs (i.e., PDZ-binding motifs or PBMs) are important for many biological processes and can be pathological when disrupted. There are hundreds of PDZ-PBM interactions reported but few have been quantitatively determined. Moreover, PDZ-PBM interactions have been identified as potential therapeutic targets. To thoroughly understand PDZ-PBM binding energetics and their specificity, we have developed a sensitive and quantitative equilibrium binding assay. Here, we describe a protocol for determining PDZ-PBM binding energetics using fluorescence anisotropy-based methodology.

Entities:  

Keywords:  CASK; Fluorescence anisotropy; PDZ domain; PDZ-binding motif; Protein–protein binding; SGEF; Scribble

Year:  2021        PMID: 34014520     DOI: 10.1007/978-1-0716-1166-1_8

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


  1 in total

1.  Spectrophotometric determination of protein concentration.

Authors:  Gerald R Grimsley; C Nick Pace
Journal:  Curr Protoc Protein Sci       Date:  2004-11
  1 in total

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