4.5 Article

Novel and highly sensitive fluorescent assay for leucine aminopeptidases

Journal

ANALYTICAL BIOCHEMISTRY
Volume 391, Issue 1, Pages 11-16

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2009.05.004

Keywords

Metallopeptidases; N-terminal hydrolysis; Fluorescent assay; HTS assay

Funding

  1. National Institute of Environmental Health Services [R37 ES02710]
  2. National Institutes of Health (NIH)/NIEHS [R01 ES013933]
  3. NIH/NIEHS Superfund Basic Research Program [P42 ES04699]

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l-Leucine aminopeptidases (LAPs) are implicated in the progress of many pathological disorders and play some regulatory roles in tumor cell proliferation, invasion, and/or angiogenesis. Thus, LAPs not only could become new diagnostic or prognostic biomarkers but also may have potential as novel molecular targets for the treatment of several cancers. Highly sensitive assays are critical for early detection of changes in LAP activity and for screening potent LAP inhibitors. In this Study, we developed a novel and highly sensitive fluorescent assay for LAPs based on Substituted aminopyridines as fluorescent reporters. This assay was at least 100- and 20-fold more sensitive than commercial colorimetric and fluorescent LAP substrates, respectively. We also showed that this assay was a useful tool for monitoring LAP activities in extracts from cancer cell lines, as well as for the high-throughput screening of inhibitors, which could lead to new cancer treatments. (C) 2009 Elsevier Inc. All rights reserved.

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