Standard Article

The Comet Assay: A Sensitive and Quantitative Method for Analysis of DNA Damage

Nucleic Acids Structure and Mapping

  1. Amaya Azqueta1,
  2. Andrew R. Collins2

Published Online: 15 DEC 2011

DOI: 10.1002/9780470027318.a9192

Encyclopedia of Analytical Chemistry

Encyclopedia of Analytical Chemistry

How to Cite

Azqueta, A. and Collins, A. R. 2011. The Comet Assay: A Sensitive and Quantitative Method for Analysis of DNA Damage. Encyclopedia of Analytical Chemistry. .

Author Information

  1. 1

    University of Navarra, Department of Nutrition, Food Science, Physiology and Toxicology, Schools of Pharmacy and Sciences, Pamplona, Spain

  2. 2

    University of Oslo, Department of Nutrition, Institute of Basic Medical Science, Oslo, Norway

Publication History

  1. Published Online: 15 DEC 2011

Abstract

The comet assay (single-cell gel electrophoresis) is a simple method for measuring DNA strand breaks in cells that are embedded in agarose and lysed to remove membranes and soluble cell constituents (including most histones). The assay depends on the ability of breaks to relax supercoiling, which allows DNA still attached to a nuclear matrix to move toward the anode under electrophoresis, forming a ‘comet tail’ when viewed by fluorescence microscopy. The percentage of DNA in the tail indicates the frequency of DNA breaks. An additional step — digestion with lesion-specific endonucleases — is introduced after lysis in order to detect different kinds of DNA damage. The assay can be calibrated to give quantitative measures of DNA damage. It has been widely used in genotoxicity testing and human biomonitoring, and also in ecogenotoxicology, as well as in basic research. We here discuss the development of the method, its principles, applications, and limitations, and attempt to dispel some fallacies that trouble the assay. We provide a detailed protocol, including a recent modification that increases the assay's throughput.