Literature DB >> 33877605

Gel-Based Analysis of Protein-Nucleic Acid Interactions.

James A W Stowell1, Terence T L Tang1, Maximilian Seidel1, Lori A Passmore2.   

Abstract

Electrophoretic mobility shift assays (EMSAs) are among the most frequently used and straightforward experiments for studying protein-nucleic acid interactions. EMSAs rely on the principle that protein-nucleic acid complexes have reduced electrophoretic mobility in a native gel matrix compared to free nucleic acid due to their larger size and reduced negative charge. Therefore, bands for the protein-nucleic acid complexes are shifted in a gel and can be distinguished from free nucleic acids. EMSAs remain a popular technique since they do not require specialist equipment and the complexes formed are easily visualized. Furthermore, the technique can be adapted to enable various aspects of protein-nucleic acid interactions to be investigated, including sequence specificity, estimated binding affinity, and binding stoichiometry.

Keywords:  Affinity measurement; Band shift assay; EMSA; Electrophoretic mobility shift assay; Protein–DNA interactions; Protein–RNA interactions

Year:  2021        PMID: 33877605     DOI: 10.1007/978-1-0716-1197-5_14

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


  11 in total

1.  A sensitive two-color electrophoretic mobility shift assay for detecting both nucleic acids and protein in gels.

Authors:  Debra Jing; Jakyoung Agnew; Wayne F Patton; Jill Hendrickson; Joseph M Beechem
Journal:  Proteomics       Date:  2003-07       Impact factor: 3.984

2.  Synthesis of RNA by in vitro transcription.

Authors:  Bertrand Beckert; Benoît Masquida
Journal:  Methods Mol Biol       Date:  2011

Review 3.  Quantitative approaches to monitor protein-nucleic acid interactions using fluorescent probes.

Authors:  John M Pagano; Carina C Clingman; Sean P Ryder
Journal:  RNA       Date:  2010-11-22       Impact factor: 4.942

4.  Electrophoretic mobility shift assay (EMSA) for detecting protein-nucleic acid interactions.

Authors:  Lance M Hellman; Michael G Fried
Journal:  Nat Protoc       Date:  2007       Impact factor: 13.491

5.  Shift-Western Blotting: Separate Analysis of Protein and DNA from Protein-DNA Complexes.

Authors:  Matthias Harbers
Journal:  Methods Mol Biol       Date:  2015

6.  Nonradioactive gel mobility shift assay using chemiluminescent detection.

Authors:  R Berger; M R Duncan; B Berman
Journal:  Biotechniques       Date:  1993-10       Impact factor: 1.993

7.  ImageJ2: ImageJ for the next generation of scientific image data.

Authors:  Curtis T Rueden; Johannes Schindelin; Mark C Hiner; Barry E DeZonia; Alison E Walter; Ellen T Arena; Kevin W Eliceiri
Journal:  BMC Bioinformatics       Date:  2017-11-29       Impact factor: 3.169

Review 8.  Metal Cations in G-Quadruplex Folding and Stability.

Authors:  Debmalya Bhattacharyya; Gayan Mirihana Arachchilage; Soumitra Basu
Journal:  Front Chem       Date:  2016-09-09       Impact factor: 5.221

9.  mRNA Deadenylation Is Coupled to Translation Rates by the Differential Activities of Ccr4-Not Nucleases.

Authors:  Michael W Webster; Ying-Hsin Chen; James A W Stowell; Najwa Alhusaini; Thomas Sweet; Brenton R Graveley; Jeff Coller; Lori A Passmore
Journal:  Mol Cell       Date:  2018-06-21       Impact factor: 17.970

10.  RNA-binding proteins distinguish between similar sequence motifs to promote targeted deadenylation by Ccr4-Not.

Authors:  Michael W Webster; James Aw Stowell; Lori A Passmore
Journal:  Elife       Date:  2019-01-02       Impact factor: 8.140

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