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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
1992-3-12
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S70201,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S70204,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S80305,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S80672,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S80673,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S80674,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S80676,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S80678,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S80680,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/S80681
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pubmed:abstractText |
Human beta 2-glycoprotein I (beta 2-GPI) is involved in cardiolipin (CL) binding of anticardiolipin antibodies (aCL) in systemic lupus erythematosus (SLE). We examined the inter-species differences of beta 2-GPI in alternation of CL binding of aCL. beta 2-GPI preparations were obtained from human, bovine, and rat sera by sequential CL--polyacrylamide affinity, DEAE--cellulose, and anti-human IgG-conjugated Sepharose CL-4B column chromatography, and they had apparent molecular weights of 50, 53, and 55 kDa respectively. Human beta 2-GPI not only enhanced CL binding by aCL in SLE but also depressed it by those in syphilis. Either bovine and rat beta 2-GPI exerted no or quite small inhibition of the binding of syphilitic aCL compared with human beta 2-GPI whereas all three species of beta 2-GPI generated binding of aCL in SLE to a similar degree. Further, a complete cDNA clone, p beta 2-GPI, was isolated from a human hepatoma cell line, HepG2, and its nucleotide sequence was analyzed. The sequences of bovine and rat counterpart molecules (beta 2-GPI) are highly homologous to that of the deduced sequence, and their corresponding regions are 84.0 and 82.5% identical to the complete domain and to the amino acid sequence 53-326 of human beta 2-GPI respectively. One of major differences appears at position 154 in human beta 2-GPI, and might be associated with the inhibitory effect on the binding of syphilitic aCL. The sequencing analysis of these beta 2-GPI proteins might provide leads to functional sites of domains which would be associated with such serological phenomena.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
|
pubmed:issn |
0953-8178
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
3
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
1217-21
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1777418-Amino Acid Sequence,
pubmed-meshheading:1777418-Animals,
pubmed-meshheading:1777418-Base Sequence,
pubmed-meshheading:1777418-Cardiolipins,
pubmed-meshheading:1777418-Cattle,
pubmed-meshheading:1777418-Cloning, Molecular,
pubmed-meshheading:1777418-DNA,
pubmed-meshheading:1777418-Glycoproteins,
pubmed-meshheading:1777418-Humans,
pubmed-meshheading:1777418-Molecular Sequence Data,
pubmed-meshheading:1777418-Rats,
pubmed-meshheading:1777418-Sequence Alignment,
pubmed-meshheading:1777418-beta 2-Glycoprotein I
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pubmed:year |
1991
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pubmed:articleTitle |
Molecular definition of human beta 2-glycoprotein I (beta 2-GPI) by cDNA cloning and inter-species differences of beta 2-GPI in alternation of anticardiolipin binding.
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pubmed:affiliation |
Immunology Laboratory, Yamasa Shoyu Co., Ltd, Chiba, Japan.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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