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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1990-2-9
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32759,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32760,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32761,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32762,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32763,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32764,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32765,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32766,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32767,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/M32768
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pubmed:abstractText |
The results presented in this paper explore the molecular basis for expression of the A48 regulatory Id (RI). A48 RI+ mAb derived from idiotypically manipulated mice molecularly resembled the A48 and UPC 10 prototypes of this system by utilizing a VHX24-Vk10 combination. Id expression by these antibodies was not restricted by a particular D region sequence, JH, or JK segment, but quantitative differences in Id expression were associated with utilization of different members of the VK10 germ-line gene families. The VL sequences of these A48 RI+ mAb has identified amino acid residues lying in four different idiotope-determining regions which may contribute to the structural correlate of this Id. A comparative sequence analysis of the VH regions of these VHX24 utilizing A48 RI+ mAb with several A48 RI+ mAb utilizing VHJ558 or VH7183 VH genes as well as a hybrid transfectoma antibody derived from two A48 RI-, VHJ558 utilizing hybridomas, all suggested that four nonconsecutive positions which lie outside the idiotope-determining regions may contribute structural elements toward expression of this Id. The VH and VL regions of the A48RI+, VHX24-Vk 10+ mAb showed low to moderate levels of somatic mutation which showed different patterns of distribution between the complementary determining region (CDR) and framework regions in the H and L chains. Although the VK sequences contained 50% of the replacement mutations in the CDR, with a replacement/silent mutation ratio of 10, the CDR of the VH sequences contained only 31% of the replacement mutations with a replacement/silent mutation ratio of 0.69.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Fructans,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Heavy Chains,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Idiotypes,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Variable Region,
http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin kappa-Chains
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
|
pubmed:issn |
0022-1767
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
|
pubmed:volume |
144
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pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
614-24
|
pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2104900-Amino Acid Sequence,
pubmed-meshheading:2104900-Animals,
pubmed-meshheading:2104900-Antibodies, Monoclonal,
pubmed-meshheading:2104900-Base Sequence,
pubmed-meshheading:2104900-Fructans,
pubmed-meshheading:2104900-Gene Rearrangement, B-Lymphocyte,
pubmed-meshheading:2104900-Genes, Immunoglobulin,
pubmed-meshheading:2104900-Immunoglobulin Heavy Chains,
pubmed-meshheading:2104900-Immunoglobulin Idiotypes,
pubmed-meshheading:2104900-Immunoglobulin Variable Region,
pubmed-meshheading:2104900-Immunoglobulin kappa-Chains,
pubmed-meshheading:2104900-Mice,
pubmed-meshheading:2104900-Molecular Sequence Data
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pubmed:year |
1990
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pubmed:articleTitle |
A molecular and structural analysis of the VH and VK regions of monoclonal antibodies bearing the A48 regulatory idiotype.
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pubmed:affiliation |
Department of Microbiology, Mount Sinai School of Medicine, New York, NY 10029.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
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