Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
1988-5-18
pubmed:abstractText
Two monoclonal anti-idiotypic antibodies (anti-Id-135 and anti-Id-14, both of the IgM class) which interact with the binding site of opioid receptors were generated. A monoclonal anti-beta-endorphin antibody (3-E7) which displays binding characteristics for opioid ligands similar to opioid receptors served as the antigen (Gramsch, C., Meo, T., Riethmüller, G., and Herz, A., (1983) J. Neurochem. 40, 1220-1226; Meo, T., Gramsch, C., Inan, R., Höllt, V., Weber, E., Herz, A., and Riethmüller, G. (1983) Proc. Natl. Acad. Sci. U.S.A. 80, 4048-4088) and the hybridomas obtained were screened for anti-idiotypic antibodies with Fab fragments of 3-E7. The anti-idiotypes were then screened for opioid binding to rat brain membrane receptors, yielding several positive clones two of which were more intensively studied. Both anti-idiotypic antibodies were about equally potent in displacing the mu- and delta-opioid receptor ligands [3H]dihydromorphine, 125I-labeled beta-endorphin, [D-Ala2, D-Leu5-3H]enkephalin and [3H]naloxone from rat brain membrane opioid receptors; no interaction was observed with the kappa-ligands [3H]ethylketazocine or [3H]bremazocine. The anti-idiotypic antibodies were able to precipitate [3H] diprenorphine binding sites from solubilized opioid receptor preparations. In addition, both antibodies showed opioid antagonistic properties as demonstrated by their abilities to block the inhibitory effect of [D-Ala2, D-Leu5-3H]enkephalin on prostaglandin E1-stimulated cAMP accumulation in NG 108-15 hybrid cells. Our findings demonstrate the successful generation of monoclonal antibodies interacting with membrane-bound and solubilized opioid receptors of the mu- and delta-type.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antibodies, Monoclonal, http://linkedlifedata.com/resource/pubmed/chemical/Antigens, http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP, http://linkedlifedata.com/resource/pubmed/chemical/Dihydromorphine, http://linkedlifedata.com/resource/pubmed/chemical/Enkephalin, Leucine, http://linkedlifedata.com/resource/pubmed/chemical/Enkephalin, Leucine-2-Alanine, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin G, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin Idiotypes, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulin M, http://linkedlifedata.com/resource/pubmed/chemical/Naloxone, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Opioid, http://linkedlifedata.com/resource/pubmed/chemical/beta-Endorphin
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
25
pubmed:volume
263
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5853-9
pubmed:dateRevised
2003-11-14
pubmed:meshHeading
pubmed-meshheading:2833518-Animals, pubmed-meshheading:2833518-Antibodies, Monoclonal, pubmed-meshheading:2833518-Antigens, pubmed-meshheading:2833518-Brain, pubmed-meshheading:2833518-Cell Membrane, pubmed-meshheading:2833518-Cyclic AMP, pubmed-meshheading:2833518-Dihydromorphine, pubmed-meshheading:2833518-Enkephalin, Leucine, pubmed-meshheading:2833518-Enkephalin, Leucine-2-Alanine, pubmed-meshheading:2833518-Hybridomas, pubmed-meshheading:2833518-Immunoglobulin G, pubmed-meshheading:2833518-Immunoglobulin Idiotypes, pubmed-meshheading:2833518-Immunoglobulin M, pubmed-meshheading:2833518-Immunosorbent Techniques, pubmed-meshheading:2833518-Mice, pubmed-meshheading:2833518-Mice, Inbred BALB C, pubmed-meshheading:2833518-Naloxone, pubmed-meshheading:2833518-Rats, pubmed-meshheading:2833518-Receptors, Opioid, pubmed-meshheading:2833518-Tumor Cells, Cultured, pubmed-meshheading:2833518-beta-Endorphin
pubmed:year
1988
pubmed:articleTitle
Monoclonal anti-idiotypic antibodies to opioid receptors.
pubmed:affiliation
Department of Neuropharmacology, Max-Planck-Institut für Psychiatrie, Planegg-Martinsried, Federal Republic of Germany.
pubmed:publicationType
Journal Article