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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2-3
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pubmed:dateCreated |
1994-1-3
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pubmed:abstractText |
The pharmacological profile of [125I][Tyr4]bombesin binding to gastrin-releasing peptide- and neuromedin B-preferring sites has been investigated in rat cerebral cortex and olfactory bulb membranes, respectively. [125I][Tyr4]bombesin specific binding to cerebral cortex membranes was displayed biphasically by gastrin releasing peptide and [D-Phe6]bombesin-(6-13)-ethyl amide. In the presence of 10 mM neuromedin B, displacement curves for bombesin-related peptides were monophasic with gastrin releasing peptide displaying approximately 100-fold higher affinity than neuromedin B. In olfactory bulb membranes, [125I][Tyr4]bombesin binding was also displaced biphasically by gastrin releasing peptide, [D-Phe6]bombesin-(6-13)-ethyl amide and neuromedin B. In the presence of 10 microM [D-Phe6]bombesin-(6-13)-ethyl ester, displacement curves were monophasic with neuromedin B possessing approximately 10-fold higher affinity than gastrin-releasing peptide. Under these conditions, successive deletion of N-terminal amino acids from bombesin-(1-14) was well tolerated at both sites, with little loss in affinity up to bombesin-(5-14). A 5- to 10-fold drop in affinity was observed at both sites with bombesin-(6-14), whilst the octapeptide acetyl-bombesin-(7-14) displayed similar affinities to bombesin-(1-14). Bombesin-(8-14), -(9-14) and -(10-14) were essentially inactive (IC50 > 10 microM). C-terminal deletion of Met24 (bombesin-(1-13)) resulted in 100-fold loss of affinity at the gastrin-releasing peptide site and complete loss of affinity at the neuromedin B site. Fragments smaller than bombesin-(1-13) were virtually inactive at either site.(ABSTRACT TRUNCATED AT 250 WORDS)
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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/Bombesin,
http://linkedlifedata.com/resource/pubmed/chemical/Gastrin-Releasing Peptide,
http://linkedlifedata.com/resource/pubmed/chemical/Gastrointestinal Hormones,
http://linkedlifedata.com/resource/pubmed/chemical/Neurokinin B,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/bombesin, Tyr(4)-,
http://linkedlifedata.com/resource/pubmed/chemical/neuromedin B
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0014-2999
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
24
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pubmed:volume |
240
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
177-84
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pubmed:dateRevised |
2003-11-14
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pubmed:meshHeading |
pubmed-meshheading:8243536-Amino Acid Sequence,
pubmed-meshheading:8243536-Animals,
pubmed-meshheading:8243536-Binding, Competitive,
pubmed-meshheading:8243536-Binding Sites,
pubmed-meshheading:8243536-Bombesin,
pubmed-meshheading:8243536-Cerebral Cortex,
pubmed-meshheading:8243536-Gastrin-Releasing Peptide,
pubmed-meshheading:8243536-Gastrointestinal Hormones,
pubmed-meshheading:8243536-Male,
pubmed-meshheading:8243536-Molecular Sequence Data,
pubmed-meshheading:8243536-Neurokinin B,
pubmed-meshheading:8243536-Olfactory Bulb,
pubmed-meshheading:8243536-Peptide Fragments,
pubmed-meshheading:8243536-Peptides,
pubmed-meshheading:8243536-Rats,
pubmed-meshheading:8243536-Rats, Sprague-Dawley,
pubmed-meshheading:8243536-Structure-Activity Relationship
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pubmed:year |
1993
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pubmed:articleTitle |
Structure-activity requirements of bombesin for gastrin-releasing peptide- and neuromedin B-preferring bombesin receptors in rat brain.
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pubmed:affiliation |
Parke-Davis Neuroscience Research Centre, Addenbrookes Hospital Site, Cambridge, UK.
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pubmed:publicationType |
Journal Article
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