MOLECULAR MECHANISMS OF APOLIPOPROTEIN B BIOGENESIS
MOLECULAR MECHANISMS OF APOLIPOPROTEIN B BIOGENESIS
批准号:
3364475
负责人:
VISHWANATH R LINGAPPA
金额:
$20.12万
依托单位国家:
美国
项目类别:
财政年份:
1991
资助国家:
美国
项目状态:
已结题
起止时间:
1991-01-01 至 1995-12-31
关键词:
Xenopus apolipoproteins blood lipoprotein biosynthesis cell free system dogs endoplasmic reticulum gene complementation genetic manipulation hyperlipoproteinemia laboratory rat lipid transport membrane proteins messenger RNA microsomes molecular cloning posttranslational modifications tissue /cell culture
中文摘要
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英文摘要
DESCRIPTION: (Adapted from the Investigator's abstract): The
investigators propose to investigate apolipoprotein B (apo B) biogenesis
and apo B-containing lipoprotein particle formation. Apo B plays a major
role in cholesterol transport. Hypercholesterolemia is a risk factor for
atherosclerosis and coronary artery disease. Some patients with elevated
serum cholesterol have a known defect in apo B structure. Many others have
uncharacterized aberrations in metabolism of apo B containing lipoproteins,
which may be related to defective assembly. An understanding of how these
diverse lesions cause hyperlipoproteinemia will require detailed knowledge
of the mechanism by which a normal lipoprotein particle is assembled and
secreted. Yet, important features of lipoprotein particle assembly are
poorly understood and not easily explained by current value of protein
biogenesis and trafficking. Recently, the investigators have discovered
unusual intermediates in the early events of apo B translocation across the
endoplasmic reticulum membrane (see Preliminary Studies) by expression of
cloned cDNAs encoding domains of apo B in both membrane-supplemented
cell-free systems and in living cells. These intermediates will be
characterized and related to stages in apo B-containing lipoprotein
particle assembly, regulation and secretion. This analysis will be
extended to later events in apo B biogenesis. Through these experiments a
better understanding of apo B biogenesis and its relationship to
lipoprotein particle formation will emerge. New insight into the
mechanisms by which apo B may be post-translationally regulated under
physiologic conditions and in hypercholesterolemic lipoprotein disorders of
humans may follow.
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