Title : Characterization of lysosomal acid lipase by site-directed mutagenesis and heterologous expression - Sheriff_1995_J.Biol.Chem_270_27766
Author(s) : Sheriff S , Du H , Grabowski GA
Ref : Journal of Biological Chemistry , 270 :27766 , 1995
Abstract :

Lysosomal acid lipase (LAL) is essential for the hydrolysis of cholesterol esters and triglycerides that are delivered to the lysosomes via the low density lipoprotein receptor system. The deficiency of LAL is associated with cholesteryl ester storage disease (CESD) and Wolman's disease (WD). We cloned the human LAL cDNA and expressed the active enzyme in the baculovirus system. Two molecular forms (M(r) approximately 41,000 and approximately 46,000) with different glycosylation were found intracellularly, and approximately 24% of the M(r) approximately 46,000 form was secreted into the medium. Tunicamycin treatment produced only an inactive M(r) approximately 41,000 form. This result implicates glycosylation occupancy in the proper folding for active-site function. Catalytic activity was greater toward cis- than trans-unsaturated fatty acid esters of 4-methylumbelliferone and toward esters with 7-carbon length acyl chains. LAL cleaved cholesterol esters and mono-, tri-, and diglycerides. Heparin had a biphasic effect on enzymatic activity with initial activation followed by inhibition. Inhibition of LAL activity by tetrahydrolipstatin and diethyl p-nitrophenyl phosphate suggested the presence of active serines in binding/catalytic domain(s) of the protein. Site-directed mutagenesis at two putative active centers, GXSXG, showed that Ser153 was important to catalytic activity, whereas Ser99 was not and neither was the catalytic nucleophile. Three reported mutations (L179P, L336P, and delta AG302 deletion) from CESD patients were created and expressed in the Sf9 cell system. None cleaved cholesterol esters, and L179P and L336P cleaved only triolein at approximately 4% of wild-type levels. These results suggest that mechanisms, in addition to LAL defects, may operate in the selective accumulation of cholesterol esters or triglycerides in CESD and WD patients.

PubMedSearch : Sheriff_1995_J.Biol.Chem_270_27766
PubMedID: 7499245
Gene_locus related to this paper: human-LIPA

Related information

Gene_locus human-LIPA

Citations formats

Sheriff S, Du H, Grabowski GA (1995)
Characterization of lysosomal acid lipase by site-directed mutagenesis and heterologous expression
Journal of Biological Chemistry 270 :27766

Sheriff S, Du H, Grabowski GA (1995)
Journal of Biological Chemistry 270 :27766