| Literature DB >> 17090660 |
Lyndon J Mitnaul1, Jenny Tian, Charlotte Burton, My-Hanh Lam, Yuping Zhu, Steve H Olson, Jonathan E Schneeweis, Paul Zuck, Shilpa Pandit, Matt Anderson, Milana M Maletic, Sherman T Waddell, Samuel D Wright, Carl P Sparrow, Erik G Lund.
Abstract
Endothelial lipase (EL) has been shown to be a critical determinant for high density lipoprotein cholesterol levels in vivo; therefore, assays that measure EL activity have become important for the discovery of small molecule inhibitors that specifically target EL. Here, we describe fluorescent Bodipy-labeled substrates that can be used in homogeneous, ultra-high-throughput kinetic assays that measure EL phospholipase or triglyceride lipase activities. Triton X-100 detergent micelles and synthetic HDL particles containing Bodipy-labeled phospholipid or Bodipy-labeled triglyceride substrates were shown to be catalytic substrates for EL, LPL, and HL. More importantly, only synthetic HDL particles containing Bodipy-labeled triglyceride were ideal substrates for EL, LPL, and HL in the presence of high concentrations of human or mouse serum. These data suggest that substrate presentation is a critical factor when determining EL activity in the presence of serum.Entities:
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Year: 2006 PMID: 17090660 DOI: 10.1194/jlr.D600041-JLR200
Source DB: PubMed Journal: J Lipid Res ISSN: 0022-2275 Impact factor: 5.922