Effect of phospholipase C and apolipophorin III on the structure and stability of lipophorin subspecies.

Four distinct subspecies of the insect hemolymph lipoprotein, lipophorin, that range in diacylglycerol (DAG) content from approximately 100 to 1000 molecules per particle, were treated with phospholipase C. Lipid analysis demonstrated that both phosphatidylcholine and phosphatidylethanolamine were h...

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Main Authors: T.K Singh, H Liu, R Bradley, D.G Scraba, R.O Ryan
Format: Article
Language:English
Published: Elsevier 1994-09-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S002222752041154X
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spelling doaj-54eeb579284f4d01b51f9690bcf0e7b82021-04-26T05:51:52ZengElsevierJournal of Lipid Research0022-22751994-09-0135915611569Effect of phospholipase C and apolipophorin III on the structure and stability of lipophorin subspecies.T.K Singh0H Liu1R Bradley2D.G Scraba3R.O Ryan4Department of Biochemistry, University of Alberta, Edmonton, Canada.Department of Biochemistry, University of Alberta, Edmonton, Canada.Department of Biochemistry, University of Alberta, Edmonton, Canada.Department of Biochemistry, University of Alberta, Edmonton, Canada.Department of Biochemistry, University of Alberta, Edmonton, Canada.Four distinct subspecies of the insect hemolymph lipoprotein, lipophorin, that range in diacylglycerol (DAG) content from approximately 100 to 1000 molecules per particle, were treated with phospholipase C. Lipid analysis demonstrated that both phosphatidylcholine and phosphatidylethanolamine were hydrolyzed to DAG. Phospholipase C was used to remove 74-82% of the phospholipid of different lipophorins and these were analyzed for aggregation. Low density lipophorin (LDLp), the largest subspecies, with a diameter of approximately 23 nm, developed turbidity (monitored by sample absorbance at 340 nm) suggesting the formation of lipoprotein aggregates. High density lipophorin-adult (HDLp-A) and high density lipophorin-wanderer 1 (HDLp-W1) also displayed an increase in A340 when incubated with phospholipase C, although the maximal increase observed was considerably less than that for LDLp on a per particle basis. Phospholipase C caused only a minimal increase in A340 in a fourth subspecies, high density lipophorin-wanderer 2 (HDLp-W2), which contains an even lower amount of DAG. Electron microscopy was used to evaluate changes in particle morphology as a result of phospholipid depletion. HDLp-W2 and HDLp-W1 showed signs of progressive aggregation and particle fusion. A similar aggregation/fusion was seen in the case of high density lipophorin adult (HDLp-A) while LDLp samples contained multiple aggregation/fusion foci and resultant very large particles. In the presence of exogenous apolipophorin III (apoLp-III), phospholipase C-induced lipophorin aggregation/fusion was prevented. Electron microscopy of LDLp and HDLp-A samples revealed that apoLp-III-stabilized, phospholipase C-treated particles had a morphology similar to that of control particles.(ABSTRACT TRUNCATED AT 250 WORDS)http://www.sciencedirect.com/science/article/pii/S002222752041154X
collection DOAJ
language English
format Article
sources DOAJ
author T.K Singh
H Liu
R Bradley
D.G Scraba
R.O Ryan
spellingShingle T.K Singh
H Liu
R Bradley
D.G Scraba
R.O Ryan
Effect of phospholipase C and apolipophorin III on the structure and stability of lipophorin subspecies.
Journal of Lipid Research
author_facet T.K Singh
H Liu
R Bradley
D.G Scraba
R.O Ryan
author_sort T.K Singh
title Effect of phospholipase C and apolipophorin III on the structure and stability of lipophorin subspecies.
title_short Effect of phospholipase C and apolipophorin III on the structure and stability of lipophorin subspecies.
title_full Effect of phospholipase C and apolipophorin III on the structure and stability of lipophorin subspecies.
title_fullStr Effect of phospholipase C and apolipophorin III on the structure and stability of lipophorin subspecies.
title_full_unstemmed Effect of phospholipase C and apolipophorin III on the structure and stability of lipophorin subspecies.
title_sort effect of phospholipase c and apolipophorin iii on the structure and stability of lipophorin subspecies.
publisher Elsevier
series Journal of Lipid Research
issn 0022-2275
publishDate 1994-09-01
description Four distinct subspecies of the insect hemolymph lipoprotein, lipophorin, that range in diacylglycerol (DAG) content from approximately 100 to 1000 molecules per particle, were treated with phospholipase C. Lipid analysis demonstrated that both phosphatidylcholine and phosphatidylethanolamine were hydrolyzed to DAG. Phospholipase C was used to remove 74-82% of the phospholipid of different lipophorins and these were analyzed for aggregation. Low density lipophorin (LDLp), the largest subspecies, with a diameter of approximately 23 nm, developed turbidity (monitored by sample absorbance at 340 nm) suggesting the formation of lipoprotein aggregates. High density lipophorin-adult (HDLp-A) and high density lipophorin-wanderer 1 (HDLp-W1) also displayed an increase in A340 when incubated with phospholipase C, although the maximal increase observed was considerably less than that for LDLp on a per particle basis. Phospholipase C caused only a minimal increase in A340 in a fourth subspecies, high density lipophorin-wanderer 2 (HDLp-W2), which contains an even lower amount of DAG. Electron microscopy was used to evaluate changes in particle morphology as a result of phospholipid depletion. HDLp-W2 and HDLp-W1 showed signs of progressive aggregation and particle fusion. A similar aggregation/fusion was seen in the case of high density lipophorin adult (HDLp-A) while LDLp samples contained multiple aggregation/fusion foci and resultant very large particles. In the presence of exogenous apolipophorin III (apoLp-III), phospholipase C-induced lipophorin aggregation/fusion was prevented. Electron microscopy of LDLp and HDLp-A samples revealed that apoLp-III-stabilized, phospholipase C-treated particles had a morphology similar to that of control particles.(ABSTRACT TRUNCATED AT 250 WORDS)
url http://www.sciencedirect.com/science/article/pii/S002222752041154X
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