Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2000-2-14
pubmed:abstractText
Proteoglycans, once thought to primarily serve as structural components of extracellular matrix, are now being focused on for their role in tissue and cell regulation, particularly angiogenesis. Many growth factors, notably the fibroblast growth family (FGF) which now numbers 19 members, bind to heparin and heparan sulfate proteoglycans and this binding has been shown to have a significant impact on the availability and activity of these growth factors. Proteoglycans can serve as both temporal and spatial regulators and effective inhibitor design may depend on disruption of these interactions. We have developed a simple assay for evaluating small inhibitors of proteoglycan-ligand binding. The assay is based on cell-free incubation of the reactants and filtration across a cationic membrane. Conditions were established that allow one to semiquantitatively determine binding constants for both direct proteoglycan as well as soluble inhibitor affinity. The assay has been demonstrated using a model heparan sulfate proteoglycan preparation (perlecan from cultured bovine endothelial cells) and FGF-2. Protamine sulfate, sucrose octasulfate, and heparin were analyzed as model inhibitor molecules. This type of assay may have wide application as a fast and easy screening tool for small potential agonists and antagonists of proteoglycan-protein interactions.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Culture Media, Conditioned, http://linkedlifedata.com/resource/pubmed/chemical/Fibroblast Growth Factor 2, http://linkedlifedata.com/resource/pubmed/chemical/Heparan Sulfate Proteoglycans, http://linkedlifedata.com/resource/pubmed/chemical/Heparin, http://linkedlifedata.com/resource/pubmed/chemical/Heparitin Sulfate, http://linkedlifedata.com/resource/pubmed/chemical/Insulin-Like Growth Factor I, http://linkedlifedata.com/resource/pubmed/chemical/Ligands, http://linkedlifedata.com/resource/pubmed/chemical/Protamines, http://linkedlifedata.com/resource/pubmed/chemical/Proteoglycans, http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Sucrose, http://linkedlifedata.com/resource/pubmed/chemical/perlecan, http://linkedlifedata.com/resource/pubmed/chemical/sucrose octasulfate
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0090-6964
pubmed:author
pubmed:issnType
Print
pubmed:volume
28
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
119-27
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:10645795-Animals, pubmed-meshheading:10645795-Biomedical Engineering, pubmed-meshheading:10645795-Cattle, pubmed-meshheading:10645795-Cell-Free System, pubmed-meshheading:10645795-Cells, Cultured, pubmed-meshheading:10645795-Culture Media, Conditioned, pubmed-meshheading:10645795-Drug Evaluation, Preclinical, pubmed-meshheading:10645795-Endothelium, Vascular, pubmed-meshheading:10645795-Fibroblast Growth Factor 2, pubmed-meshheading:10645795-Heparan Sulfate Proteoglycans, pubmed-meshheading:10645795-Heparin, pubmed-meshheading:10645795-Heparitin Sulfate, pubmed-meshheading:10645795-Humans, pubmed-meshheading:10645795-Insulin-Like Growth Factor I, pubmed-meshheading:10645795-Kinetics, pubmed-meshheading:10645795-Ligands, pubmed-meshheading:10645795-Protamines, pubmed-meshheading:10645795-Protein Binding, pubmed-meshheading:10645795-Proteoglycans, pubmed-meshheading:10645795-Recombinant Proteins, pubmed-meshheading:10645795-Sucrose
pubmed:year
2000
pubmed:articleTitle
A simple assay for evaluating inhibitors of proteoglycan-ligand binding.
pubmed:affiliation
Department of Chemical Engineering, Virginia Polytechnic Institute and State University, Blacksburg 24061-0211, USA. kforsten@vt.edu
pubmed:publicationType
Journal Article, In Vitro, Research Support, U.S. Gov't, P.H.S., Research Support, U.S. Gov't, Non-P.H.S.