Measuring enzyme activity in single cells

Trends Biotechnol. 2011 May;29(5):222-30. doi: 10.1016/j.tibtech.2011.01.003. Epub 2011 Feb 11.

Abstract

Seemingly identical cells can differ in their biochemical state, function and fate, and this variability plays an increasingly recognized role in organism-level outcomes. Cellular heterogeneity arises in part from variation in enzyme activity, which results from interplay between biological noise and multiple cellular processes. As a result, single-cell assays of enzyme activity, particularly those that measure product formation directly, are crucial. Recent innovations have yielded a range of techniques to obtain these data, including image-, flow- and separation-based assays. Research to date has focused on easy-to-measure glycosylases and clinically-relevant kinases. Expansion of these techniques to a wider range and larger number of enzymes will answer contemporary questions in proteomics and glycomics, specifically with respect to biological noise and cellular heterogeneity.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Cells / metabolism*
  • Cytological Techniques / methods*
  • Electrophoresis, Capillary / methods
  • Enzymes / metabolism*
  • Flow Cytometry / methods
  • Microscopy / methods

Substances

  • Enzymes