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Peptides that mimic glycosaminoglycans: high-affinity ligands for a hyaluronan binding domain.

Identifieur interne : 003430 ( Main/Exploration ); précédent : 003429; suivant : 003431

Peptides that mimic glycosaminoglycans: high-affinity ligands for a hyaluronan binding domain.

Auteurs : M R Ziebell [États-Unis] ; Z G Zhao ; B. Luo ; Y. Luo ; E A Turley ; G D Prestwich

Source :

RBID : pubmed:11731299

Descripteurs français

English descriptors

Abstract

Hyaluronan (HA) is a non-sulfated glycosaminoglycan (GAG) that promotes motility, adhesion, and proliferation in mammalian cells, as mediated by cell-surface HA receptors. We sought to identify non-carbohydrate ligands that would bind to and activate cell-surface HA receptors. Such analogs could have important therapeutic uses in the treatment of cancer, wound healing, and arthritis, since such ligands would be resistant to degradation by hyaluronidase (HAse).

DOI: 10.1016/s1074-5521(01)00078-3
PubMed: 11731299


Affiliations:


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Le document en format XML

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<nlm:affiliation>Department of Physiology and Biophysics, The University at Stony Brook, NY 11794-8661, USA.</nlm:affiliation>
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<name sortKey="Zhao, Z G" sort="Zhao, Z G" uniqKey="Zhao Z" first="Z G" last="Zhao">Z G Zhao</name>
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<term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Binding Sites</term>
<term>Binding, Competitive</term>
<term>Extracellular Matrix Proteins (antagonists & inhibitors)</term>
<term>Extracellular Matrix Proteins (metabolism)</term>
<term>Glycosaminoglycans (antagonists & inhibitors)</term>
<term>Glycosaminoglycans (chemistry)</term>
<term>Humans</term>
<term>Hyaluronan Receptors (metabolism)</term>
<term>Hyaluronic Acid (antagonists & inhibitors)</term>
<term>Hyaluronic Acid (chemistry)</term>
<term>Ligands</term>
<term>Models, Molecular</term>
<term>Molecular Mimicry</term>
<term>Oligopeptides (chemistry)</term>
<term>Oligopeptides (metabolism)</term>
<term>Peptide Library</term>
<term>Protein Binding</term>
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<term>Acide hyaluronique ()</term>
<term>Acide hyaluronique (antagonistes et inhibiteurs)</term>
<term>Animaux</term>
<term>Banque de peptides</term>
<term>Fixation compétitive</term>
<term>Glycosaminoglycanes ()</term>
<term>Glycosaminoglycanes (antagonistes et inhibiteurs)</term>
<term>Humains</term>
<term>Liaison aux protéines</term>
<term>Ligands</term>
<term>Mimétisme moléculaire</term>
<term>Modèles moléculaires</term>
<term>Oligopeptides ()</term>
<term>Oligopeptides (métabolisme)</term>
<term>Protéines de la matrice extracellulaire (antagonistes et inhibiteurs)</term>
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<term>Relation structure-activité</term>
<term>Sites de fixation</term>
<term>Séquence d'acides aminés</term>
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<term>Extracellular Matrix Proteins</term>
<term>Glycosaminoglycans</term>
<term>Hyaluronic Acid</term>
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<term>Glycosaminoglycans</term>
<term>Hyaluronic Acid</term>
<term>Oligopeptides</term>
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<term>Amino Acid Sequence</term>
<term>Animals</term>
<term>Binding Sites</term>
<term>Binding, Competitive</term>
<term>Humans</term>
<term>Ligands</term>
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<term>Molecular Mimicry</term>
<term>Peptide Library</term>
<term>Protein Binding</term>
<term>Structure-Activity Relationship</term>
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<term>Oligopeptides</term>
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<div type="abstract" xml:lang="en">Hyaluronan (HA) is a non-sulfated glycosaminoglycan (GAG) that promotes motility, adhesion, and proliferation in mammalian cells, as mediated by cell-surface HA receptors. We sought to identify non-carbohydrate ligands that would bind to and activate cell-surface HA receptors. Such analogs could have important therapeutic uses in the treatment of cancer, wound healing, and arthritis, since such ligands would be resistant to degradation by hyaluronidase (HAse).</div>
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