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PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
25
pubmed:dateCreated
1990-10-9
pubmed:abstractText
We have isolated four insulin-like growth factor binding proteins (IGFBPs) from adult human serum by insulin-like growth factor (IGF) I affinity chromatography and high performance liquid chromatography. A 36-kDa binding protein (BP), not digestible with N-glycanase, is increased in patients with extrapancreatic tumor hypoglycemia and during IGF I administration in healthy adults. Its 38 NH2-terminal amino acids are identical to those of an IGFBP sequence derived from a human cDNA that cross-hybridizes with the rat IGFBP-2 cDNA. With probes encoding a NH2-terminal, COOH-terminal, and a middle region of this protein we have obtained three cDNA clones from a Hep G2 cDNA library; one encodes human IGFBP-2, and the other two presumably represent unspliced heteronuclear and alternatively spliced mRNA, respectively. A 28-30-kDa IGFBP represents a novel BP species in human serum. Its 30 NH2-terminal amino acids are not homologous to IGFBP-1, -2, or -3. It is not digestible with N-glycanase and does not bind 125I-IGF I. The NH2-terminal sequences of a 42/45- and a 31-kDa IGFBP are identical to that of human IGFBP-3. The 42/45-kDa proteins are two glycosylation variants of BP-3. The 31-kDa protein presumably is a degradation product of BP-3 that lacks the COOH terminus. It is likely that the different IGFBPs modulate auto-/paracrine and endocrine effects of IGFs on growth and metabolism in a different and specific manner.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
5
pubmed:volume
265
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
14892-8
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:1697583-Adult, pubmed-meshheading:1697583-Amino Acid Sequence, pubmed-meshheading:1697583-Animals, pubmed-meshheading:1697583-Base Sequence, pubmed-meshheading:1697583-Carcinoma, Hepatocellular, pubmed-meshheading:1697583-Carrier Proteins, pubmed-meshheading:1697583-Cell Line, pubmed-meshheading:1697583-Chromatography, Affinity, pubmed-meshheading:1697583-Cloning, Molecular, pubmed-meshheading:1697583-Gene Library, pubmed-meshheading:1697583-Humans, pubmed-meshheading:1697583-Hypoglycemia, pubmed-meshheading:1697583-Insulin-Like Growth Factor Binding Proteins, pubmed-meshheading:1697583-Insulin-Like Growth Factor I, pubmed-meshheading:1697583-Ligands, pubmed-meshheading:1697583-Liver Neoplasms, pubmed-meshheading:1697583-Molecular Sequence Data, pubmed-meshheading:1697583-Neoplasms, pubmed-meshheading:1697583-Oligonucleotide Probes, pubmed-meshheading:1697583-Plasmids, pubmed-meshheading:1697583-RNA, Messenger, pubmed-meshheading:1697583-Reference Values, pubmed-meshheading:1697583-Sequence Homology, Nucleic Acid, pubmed-meshheading:1697583-Somatomedins
pubmed:year
1990
pubmed:articleTitle
Isolation from adult human serum of four insulin-like growth factor (IGF) binding proteins and molecular cloning of one of them that is increased by IGF I administration and in extrapancreatic tumor hypoglycemia.
pubmed:affiliation
Department of Medicine, University Hospital, Zurich CH-8091, Switzerland.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't