TRIFLUOROACETYLATED 62-KDA PROTEIN AS POSSIBLE IMMUNOGEN IN HALOTHANE HEPATITIS
TRIFLUOROACETYLATED 62-KDA PROTEIN AS POSSIBLE IMMUNOGEN IN HALOTHANE HEPATITIS
批准号:
3878918
负责人:
K KORZEKWA
金额:
$0.0万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
中文摘要
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英文摘要
Sera from halothane hepatitis patients have been shown to contain
antibodies that react with several trifluoroacetylated proteins (100 kDa,
80 kDa, 63 kDa, 59 kDa, 57 kDa, and 54 kDa) purified from the livers of
halothane treated rats. These findings suggest that similar
trifluoroacetylated proteins are the immunogens responsible for the
formation of the patients' antibodies and perhaps the subsequent
development of hepatitis. This year a nearly full-length cDNA clone of the
63 kDa protein has been isolated from a Lambda gt11 rat liver cDNA library.
Based upon the encoded sequence of this clone and the sequences of the
N-terminal and several internal peptides of the purified protein, 63 kDa
has been identified as calreticulin. Genomic DNA preparations from rat
liver were probed with a fragment encompassing the cloned open reading
frame. Strong homology was found to a single genomic region, with limited
homology to a second region detected after prolonged autoradiography,
indicating that the 63 kDa protein is not part of a multi-gene family.
Immunoblotting of several tissues with the anti-63 kDa antibody indicated
that the protein was present in all tissues of body, with highest
concentrations being in the liver, testes, and adipose tissue. Calreticulin
is a calcium binding protein of the endoplasmic reticulum in non-muscle
cells and the sarcoplasmic reticulum in muscle cells. Calreticulin is
thought to have a role in calcium homeostasis by acting as a storage
reservoir of calcium. Since the present study has shown that calreticulin
can be a target of the reactive metabolites of drugs, this raises the
possibility that the calcium binding capacity of this protein can be
altered by drugs and as a result play a role in the toxicity produced not
only by halothane, but also by other drugs.
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STUDIES ON THE CONVERSION OF ANDROGENS TO ESTROGENS BY AROMATASE
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批准号:3838486
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
THEORETICAL MODELS FOR CYTOCHROME P-450 MEDIATED HYDROGEN ATOM ABSTRACTION
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批准号:3878919
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
STUDIES ON THE ACTIVE SITES AND MECHANISMS OF CYTOCHROME P450
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批准号:3752725
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
STUDIES ON THE ACTIVE SITES OF CYTOCHROMES P-450
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批准号:3878913
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
STUDIES ON THE ACTIVE SITES AND MECHANISMS OF CYTOCHROME P450
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批准号:3838460
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
THEORETICAL MODELS FOR CYTOCHROME P450 MEDIATED OXIDATIONS
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批准号:3838459
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
STUDIES ON THE ACTIVE SITES AND MECHANISMS OF CYTOCHROME P450
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批准号:3853571
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
THEORETICAL MODELS FOR CYTOCHROME P450 MEDIATED OXIDATIONS
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批准号:3853570
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
STUDIES ON THE ACTIVE SITES OF CYTOCHROMES P-450
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批准号:3942797
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
A UNIQUE TESTOSTERONE METABOLITE--17BETA-HYDROXY 4,6-ANDROSTADIENE-3-ONE
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批准号:3920011
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
STUDIES ON THE ACTIVE SITES OF CYTOCHROMES P-450
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批准号:3920013
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
A UNIQUE TESTOSTERONE METABOLITE--17BETA-HYDROXY 4,6-ANDROSTADIENE-3-ONE
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批准号:3942794
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
STUDIES ON THE CONVERSION OF ANDROGENS TO ESTROGENS BY AROMATASE
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批准号:3752742
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
THEORETICAL MODELS FOR CYTOCHROME P450 MEDIATED OXIDATIONS
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批准号:3752724
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项目类别:
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资助金额:$0.0万
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财政年份:--
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负责人:K KORZEKWA
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依托单位:
海外基金