Literature DB >> 17417012

Yeast two-hybrid screening.

Jodi Maple1, Simon G Møller.   

Abstract

Yeast two-hybrid screening represents a sensitive in vivo method for the identification and analysis of protein-protein interactions. The principle is based on the ability of a separate DNA-binding domain (DNA-BD) and activation domain (AD) to reconstitute a functional transactivator when brought into proximity. In the MATCHMAKER yeast two-hybrid system, a bait protein is expressed as a fusion to the GAL4 DNA-BD, whereas the prey protein is expressed as a fusion to the GAL4 AD. When a bait and a prey protein interact, the DNA-BD and AD form a functional transactivator, resulting in activation of reporter gene expression in yeast reporter strains. The method described in this chapter can be used to identify novel protein interactions, analyze protein-protein interactions between two known proteins, as well as dissect interacting protein domains.

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Year:  2007        PMID: 17417012     DOI: 10.1007/978-1-59745-257-1_15

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


  2 in total

Review 1.  DNA-protein interaction: identification, prediction and data analysis.

Authors:  Abbasali Emamjomeh; Darush Choobineh; Behzad Hajieghrari; Nafiseh MahdiNezhad; Amir Khodavirdipour
Journal:  Mol Biol Rep       Date:  2019-03-26       Impact factor: 2.316

2.  Construction and identification of a yeast two-hybrid bait vector and its effect on the growth of yeast cells and the self-activating function of reporter genes for screening of HPV18 E6-interacting protein.

Authors:  Quan Mei; Shuang Li; Ping Liu; Ling Xi; Shixuan Wang; Yuhan Meng; Jie Liu; Xinwei Yang; Yunping Lu; Hui Wang
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2010-02-14
  2 in total

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