Source:http://linkedlifedata.com/resource/pubmed/id/19740109
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
20
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pubmed:dateCreated |
2009-10-2
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pubmed:abstractText |
In the present study, we describe the production of transgenic silkworms expressing a recombinant mouse mAb in their cocoons. Two transgenic lines, L- and H-, were generated that carried cDNAs encoding the L- and H-chains of a mouse IgG mAb, respectively, under the control of the enhancer-linked sericin-1 promoter. Cocoon protein analysis indicated that the IgG L- or H-chain was secreted into the cocoons of each line. We also produced a transgenic line designated L/H, which carried both cDNAs, by crossing the L- and H-lines. This line efficiently produced the recombinant mAb as a fully assembled H(2)L(2) tetramer in its cocoons, with negligible L- or H-chain monomer and H-chain dimer production. Thus, the H(2)L(2) tetramer was synthesized in, and secreted from, the middle silk gland cells. Crossing of the L/H-line with a transgenic line expressing a baculovirus-derived trans-activator produced a 2.4-fold increase in mAb expression. The recombinant mAb was extracted from the cocoons with a buffer containing 3 m urea and purified by protein G affinity column chromatography. The antigen-binding affinity of the purified recombinant mAb was identical to that of the native mAb produced by a hybridoma. Analysis of the structure of the N-glycans attached to the recombinant mAb revealed that the mAb contained high mannose-, hybrid- and complex-type N-glycans. By contrast, insect-specific paucimannose-type glycans were not detected. Fucose residues alpha-1,3- and alpha-1,6-linked to the core N-acetylglucosamine residue, both of which are found in insect N-glycans, were not observed in the N-glycans of the mAb.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Anti-Idiotypic,
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Sericins,
http://linkedlifedata.com/resource/pubmed/chemical/Silk,
http://linkedlifedata.com/resource/pubmed/chemical/anti-IgG
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1742-4658
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
276
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
5806-20
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pubmed:meshHeading |
pubmed-meshheading:19740109-Animals,
pubmed-meshheading:19740109-Animals, Genetically Modified,
pubmed-meshheading:19740109-Antibodies, Anti-Idiotypic,
pubmed-meshheading:19740109-Antibodies, Monoclonal,
pubmed-meshheading:19740109-Bombyx,
pubmed-meshheading:19740109-Chromatography, High Pressure Liquid,
pubmed-meshheading:19740109-Mice,
pubmed-meshheading:19740109-Promoter Regions, Genetic,
pubmed-meshheading:19740109-Recombinant Fusion Proteins,
pubmed-meshheading:19740109-Sericins,
pubmed-meshheading:19740109-Silk,
pubmed-meshheading:19740109-Spectrometry, Mass, Matrix-Assisted Laser...
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pubmed:year |
2009
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pubmed:articleTitle |
Production of a recombinant mouse monoclonal antibody in transgenic silkworm cocoons.
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pubmed:affiliation |
Neosilk Co., Ltd, Higashihiroshima, Hiroshima, Japan.
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pubmed:publicationType |
Journal Article
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