Lipolysis of very low density lipoproteins by heparan sulfate proteoglycan-bound lipoprotein lipase.

Abstract:

:An in vitro assay to study lipolysis of very low density lipoproteins (VLDL) by heparan sulfate proteoglycan (HSPG-bound lipoprotein lipase (LPL) was developed. Optimal conditions for VLDL lipolysis by HSPG-bound LPL were obtained by incubating plastic wells with 0.5 microg HSPG and 1.5 microg LPL, subsequently. Control experiments with heparinase indicate that at least 90% of the LPL activity is derived from LPL bound to heparan sulfate chains. For HSPG-LPL-mediated lipolysis, the apparent Km and Vmax values were 0.36 +/- 0.11 mM VLDL-triglycerides and 1.2 +/- 0.1 microM free fatty acids/min x ng LPL, respectively. The mean intra-assay and inter-assay coefficients of variance were 5% and 8%, respectively.

journal_name

J Lipid Res

authors

de Man FH,de Beer F,van der Laarse A,Smelt AH,Havekes LM

subject

Has Abstract

pub_date

1997-12-01 00:00:00

pages

2465-72

issue

12

eissn

0022-2275

issn

1539-7262

journal_volume

38

pub_type

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