Journal Article

A high-throughput assay for the comprehensive profiling of DNA ligase fidelity

Gregory J. S. Lohman, Robert J. Bauer, Nicole M. Nichols, Laurie Mazzola, Joanna Bybee, Danielle Rivizzigno, Elizabeth Cantin and Thomas C. Evans

in Nucleic Acids Research

Volume 44, issue 2, pages e14-e14
Published in print January 2016 | ISSN: 0305-1048
Published online September 2015 | e-ISSN: 1362-4962 | DOI:

More Like This

Show all results sharing these subjects:

  • Enzymology
  • Molecular Biology and Genetics


Show Summary Details


DNA ligases have broad application in molecular biology, from traditional cloning methods to modern synthetic biology and molecular diagnostics protocols. Ligation-based detection of polynucleotide sequences can be achieved by the ligation of probe oligonucleotides when annealed to a complementary target sequence. In order to achieve a high sensitivity and low background, the ligase must efficiently join correctly base-paired substrates, while discriminating against the ligation of substrates containing even one mismatched base pair. In the current study, we report the use of capillary electrophoresis to rapidly generate mismatch fidelity profiles that interrogate all 256 possible base-pair combinations at a ligation junction in a single experiment. Rapid screening of ligase fidelity in a 96-well plate format has allowed the study of ligase fidelity in unprecedented depth. As an example of this new method, herein we report the ligation fidelity of Thermus thermophilus DNA ligase at a range of temperatures, buffer pH and monovalent cation strength. This screen allows the selection of reaction conditions that maximize fidelity without sacrificing activity, while generating a profile of specific mismatches that ligate detectably under each set of conditions.

Journal Article.  8044 words.  Illustrated.

Subjects: Enzymology ; Molecular Biology and Genetics

Users without a subscription are not able to see the full content. Please, subscribe or login to access all content.