Source:http://linkedlifedata.com/resource/pubmed/id/11931616
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2002-4-4
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pubmed:abstractText |
The osteogenic growth peptide (OGP) is a key factor in the mechanism of the systemic osteogenic response to local bone marrow injury. When administered in vivo, OGP stimulates osteogenesis and hematopoiesis. The C-terminal pentapeptide OGP(10-14) is the minimal amino acid sequence that retains the full OGP-like activity. Apparently, it is also the physiologic active form of OGP. Residues Tyr(10), Phe(12), Gly(13), and Gly(14) of OGP are essential for the OGP(10-14) activity. The present study explored the functional role of the peptide bonds, carboxyl and amino terminal groups, and conformational freedom in OGP(10-14). Transformations replacing the peptide bonds with surrogates such as Psi(CH(2)NH), Psi(CONMe), and Psi(CH(2)CH(2)) demonstrated that amide bonds do not contribute significantly to OGP(10-14) bioactivity. End-to-end cyclization yielded the fully bioactive cyclic pentapeptide c(Tyr-Gly-Phe-Gly-Gly). The retroinverso analogue c(Gly-Gly-phe-Gly-tyr), a cyclostereoisomer of c(Tyr-Gly-Phe-Gly-Gly), is at least as potent as the parent cyclic pentapeptide. The unique structure-activity relations revealed in this study suggest that the spatial presentation of the Tyr and Phe side chains has a major role in the productive interaction of OGP(10-14) and its truncated and conformationally constrained analogues with their cognate cellular target.
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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/Endorphins,
http://linkedlifedata.com/resource/pubmed/chemical/Growth Substances,
http://linkedlifedata.com/resource/pubmed/chemical/Histones,
http://linkedlifedata.com/resource/pubmed/chemical/Intercellular Signaling Peptides...,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides, Cyclic,
http://linkedlifedata.com/resource/pubmed/chemical/historphin,
http://linkedlifedata.com/resource/pubmed/chemical/osteogenic growth peptide
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0022-2623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
11
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pubmed:volume |
45
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1624-32
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11931616-Animals,
pubmed-meshheading:11931616-Cell Division,
pubmed-meshheading:11931616-Cell Line,
pubmed-meshheading:11931616-Colony-Forming Units Assay,
pubmed-meshheading:11931616-Endorphins,
pubmed-meshheading:11931616-Female,
pubmed-meshheading:11931616-Growth Substances,
pubmed-meshheading:11931616-Histones,
pubmed-meshheading:11931616-Intercellular Signaling Peptides and Proteins,
pubmed-meshheading:11931616-Mice,
pubmed-meshheading:11931616-Ovariectomy,
pubmed-meshheading:11931616-Peptide Fragments,
pubmed-meshheading:11931616-Peptides,
pubmed-meshheading:11931616-Peptides, Cyclic,
pubmed-meshheading:11931616-Rats,
pubmed-meshheading:11931616-Stereoisomerism,
pubmed-meshheading:11931616-Structure-Activity Relationship
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pubmed:year |
2002
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pubmed:articleTitle |
Bioactive pseudopeptidic analogues and cyclostereoisomers of osteogenic growth peptide C-terminal pentapeptide, OGP(10-14).
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pubmed:affiliation |
Bone Laboratory and Department of Oral Biology, Institute of Dental Sciences, The Hebrew University of Jerusalem, Jerusalem 91120, Israel.
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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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