Literature DB >> 28815504

Purification and In Vitro Characterization of Zinc Finger Recombinases.

Femi J Olorunniji1, Susan J Rosser2, W Marshall Stark3.   

Abstract

Zinc finger recombinases (ZFRs) are designer site-specific recombinases that have been adapted for a variety of genome editing purposes. Due to their modular nature, ZFRs can be customized for targeted sequence recognition and recombination. There has been substantial research on the in vivo properties and applications of ZFRs; however, in order to fully understand and customize them, it will be necessary to study their properties in vitro. Experiments in vitro can allow us to optimize catalytic activities, improve target specificity, measure and minimize off-target activity, and characterize key steps in the recombination pathway that might be modified to improve performance. Here, we present a straightforward set of protocols for the expression and purification of ZFRs, an assay system for catalytic proficiency in vitro and bandshift assays for detection of sequence-specific DNA interactions.

Keywords:  In vitro recombination; Serine recombinase; Site-specific recombination; ZFR; Zinc finger recombinase

Mesh:

Substances:

Year:  2017        PMID: 28815504     DOI: 10.1007/978-1-4939-7169-5_15

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


  2 in total

Review 1.  Engineering altered protein-DNA recognition specificity.

Authors:  Adam J Bogdanove; Andrew Bohm; Jeffrey C Miller; Richard D Morgan; Barry L Stoddard
Journal:  Nucleic Acids Res       Date:  2018-06-01       Impact factor: 16.971

2.  Pairing of single mutations yields obligate Cre-type site-specific recombinases.

Authors:  Jenna Hoersten; Gloria Ruiz-Gómez; Felix Lansing; Teresa Rojo-Romanos; Lukas Theo Schmitt; Jan Sonntag; M Teresa Pisabarro; Frank Buchholz
Journal:  Nucleic Acids Res       Date:  2022-01-25       Impact factor: 16.971

  2 in total

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