Literature DB >> 28882064

Development of a novel fluorescent activity assay for lecithin:cholesterol acyltransferase.

Toshihiro Sakurai1,2, Akiko Sakurai1, Boris L Vaisman1, Takafumi Nishida1, Edward B Neufeld1, Stephen J Demosky1, Maureen L Sampson3, Robert D Shamburek1, Lita A Freeman1, Alan T Remaley1,3.   

Abstract

Background Lecithin:cholesterol acyltransferase (LCAT) is a plasma enzyme that esterifies cholesterol. Recombinant human LCAT (rhLCAT) is now being developed as an enzyme replacement therapy for familial LCAT deficiency and as a possible treatment for acute coronary syndrome. The current 'gold standard' assay for LCAT activity involves the use of radioisotopes, thus making it difficult for routine clinical use. Methods We have developed a novel and more convenient LCAT activity assay using fluorescence-labelled cholesterol (BODIPY-cholesterol), which is incorporated into proteoliposomes as a substrate instead of radiolabelled cholesterol. Results The apparent Km and Vmax were 31.5  µmol/L and 55.8 nmol/h/nmoL, rhLCAT, respectively, for the 3H-cholesterol method and 103.1  µmol/L and 13.4 nmol/h/nmol rhLCAT, respectively, for the BODIPY-cholesterol method. Although the two assays differed in their absolute units of LCAT activity, there was a good correlation between the two test assays ( r = 0.849, P < 1.6 × 10-7, y = 0.1378x + 1.106). The BODIPY-cholesterol assay had an intra-assay CV of 13.7%, which was superior to the intra-assay CV of 20.8% for the radioisotopic assay. The proteoliposome substrate made with BODIPY-cholesterol was stable to storage for at least 10 months. The reference range ( n = 20) for the fluorescent LCAT activity assay was 4.6-24.1 U/mL/h in healthy subjects. Conclusions In summary, a novel fluorescent LCAT activity assay that utilizes BODIPY-cholesterol as a substrate is described that yields comparable results to the radioisotopic method.

Entities:  

Keywords:  Lecithin:cholesterol acyltransferase; cholesterol; esterified cholesterol; fluorescence

Mesh:

Substances:

Year:  2017        PMID: 28882064     DOI: 10.1177/0004563217733285

Source DB:  PubMed          Journal:  Ann Clin Biochem        ISSN: 0004-5632            Impact factor:   2.057


  4 in total

1.  Untargeted metabolomics profiles delineate metabolic alterations in mouse plasma during lung carcinoma development using UPLC-QTOF/MS in MSE mode.

Authors:  Huan Wu; Yang Chen; Zegeng Li; Xianhua Liu
Journal:  R Soc Open Sci       Date:  2018-09-19       Impact factor: 2.963

2.  ApoA-I-Mediated Lipoprotein Remodeling Monitored with a Fluorescent Phospholipid.

Authors:  Edward B Neufeld; Masaki Sato; Scott M Gordon; Vinay Durbhakula; Nicolas Francone; Angel Aponte; Gizem Yilmaz; Denis Sviridov; Maureen Sampson; Jingrong Tang; Milton Pryor; Alan T Remaley
Journal:  Biology (Basel)       Date:  2019-07-12

3.  Mathematical Modelling of Material Transfer to High-Density Lipoprotein (HDL) upon Triglyceride Lipolysis by Lipoprotein Lipase: Relevance to Cardioprotective Role of HDL.

Authors:  Svetlana Schekatolina; Viktoriia Lahovska; Aleksandr Bekshaev; Sergey Kontush; Wilfried Le Goff; Anatol Kontush
Journal:  Metabolites       Date:  2022-07-06

4.  LCAT protects against Lipoprotein-X formation in a murine model of drug-induced intrahepatic cholestasis.

Authors:  Marcelo J A Amar; Lita A Freeman; Takafumi Nishida; Maureen L Sampson; Milton Pryor; Boris L Vaisman; Edward B Neufeld; Sotirios K Karathanasis; Alan T Remaley
Journal:  Pharmacol Res Perspect       Date:  2019-12-29
  4 in total

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