Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
32
pubmed:dateCreated
2002-8-5
pubmed:abstractText
Heparan sulfate (HS) regulates the kinetics of fibroblast growth factor 2 (FGF2)-stimulated intracellular signaling and differentially activates cell proliferation of cells expressing different FGF receptors (FGFRs). Evidence suggests that HS interacts with both FGFs and FGFRs to form active ternary signaling complexes. Here we compare the interactions of two FGFRs with HS. We show that the ectodomains of FGFR1 IIIc and FGFR2 IIIc exhibit specific interactions with different characteristics for both heparin and porcine mucosal HS. These glycans are both known to activate FGF signaling via these receptors. FGFR2 interacts with a higher apparent affinity than FGFR1 despite both involving 6-O-, 2-O-, and N-sulfates. FGFR1 and FGFR2 bind heparin with mean association rate constants of 1.9 x 10(5) and 2.1 x 10(6) m(-1)s(-1), respectively, and dissociation rate constants of 1.2 x 10(-2) and 2.7 x 10(-2) s(-1), respectively. These produced calculated affinities of 63 and 13 nm, respectively. Hence, FGFR1 and FGFR2 bind to heparin chains with markedly different kinetics and affinities. We propose a mechanistic model where the kinetic parameters of the HS/FGFR interaction are a key element regulating the formation of ternary complexes and the resulting FGF signaling outcomes.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
9
pubmed:volume
277
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
28554-63
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:12034712-Animals, pubmed-meshheading:12034712-Binding, Competitive, pubmed-meshheading:12034712-Biotinylation, pubmed-meshheading:12034712-Cattle, pubmed-meshheading:12034712-Dose-Response Relationship, Drug, pubmed-meshheading:12034712-Electrophoresis, Polyacrylamide Gel, pubmed-meshheading:12034712-Enzyme-Linked Immunosorbent Assay, pubmed-meshheading:12034712-Fibroblast Growth Factors, pubmed-meshheading:12034712-Glycosaminoglycans, pubmed-meshheading:12034712-Heparin, pubmed-meshheading:12034712-Heparitin Sulfate, pubmed-meshheading:12034712-Kinetics, pubmed-meshheading:12034712-Lung, pubmed-meshheading:12034712-Models, Biological, pubmed-meshheading:12034712-Protein Binding, pubmed-meshheading:12034712-Protein Structure, Tertiary, pubmed-meshheading:12034712-Receptor, Fibroblast Growth Factor, Type 1, pubmed-meshheading:12034712-Receptor, Fibroblast Growth Factor, Type 2, pubmed-meshheading:12034712-Receptor Protein-Tyrosine Kinases, pubmed-meshheading:12034712-Receptors, Fibroblast Growth Factor, pubmed-meshheading:12034712-Signal Transduction, pubmed-meshheading:12034712-Swine
pubmed:year
2002
pubmed:articleTitle
Fibroblast growth factor receptors 1 and 2 interact differently with heparin/heparan sulfate. Implications for dynamic assembly of a ternary signaling complex.
pubmed:affiliation
School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, United Kingdom.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't