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dc.creatorPatti, Joseph M.
dc.creatorFoster, Timothy J.
dc.creatorJosefsson, Elisabet
dc.creatorEidhin, Deidre Ni
dc.creatorHook, Magnus A. O.
dc.creatorPerkins, Samuel E.
dc.date.accessioned2019-06-17T16:58:03Z
dc.date.available2019-06-17T16:58:03Z
dc.date.issued2004-01-20
dc.identifier.urihttp://hdl.handle.net/1969.1/176745
dc.description.abstractIsolated extracellular matrix-binding proteins, designated ClfB, SdrC, SdrD and SdrE, and their corresponding amino acid and nucleic acid sequences and motifs are described. The proteins, peptides, fragments thereof or antigenic portions thereof are useful for the prevention, inhibition, treatment and diagnosis of S. aureus infection and as scientific research tools. Further, antibodies or antibody fragments to the proteins, peptides, fragments thereof or antigenic portions thereof are also useful for the prevention, inhibition, treatment and diagnosis of S. aureus infection. In particular, the proteins or antibodies thereof may be administered to wounds or used to coat biomaterials to act as blocking agents to prevent or inhibit the binding of S. aureus to wounds or biomaterials. ClfB is a cell-wall associated protein having a predicted molecular weight of approximately 88 kDa and an apparent molecular weight of approximately 124 kDa, which binds both soluble and immobilized fibrinogen. ClfB binds both the alpha and beta chains of fibrinogen and acts as a clumping factor. SdrC, SdrD and SdrE are cell-wall associated proteins that exhibit cation-dependent ligand binding to the extracellular matrix. It has been discovered that in the A region of SdrC, SdrD, SdrE, ClfA and ClfB, there is a highly conserved amino acid sequence that can be used to derive a consensus motif of TYTFTDYVD (SEQ ID NO: 16).en
dc.languageeng
dc.publisherUnited States. Patent and Trademark Office
dc.rightsPublic Domain (No copyright - United States)en
dc.rights.urihttp://rightsstatements.org/vocab/NoC-US/1.0/
dc.titleExtracellular matrix-binding proteins from staphylococcus aureusen
dc.typeUtility patenten
dc.format.digitalOriginreformatted digitalen
dc.description.countryUS
dc.contributor.assigneeInhibitex, Inc.
dc.contributor.assigneeBioresearch, Ireland
dc.contributor.assigneeThe Texas A&M University System
dc.identifier.patentapplicationnumber09/200650
dc.subject.uspcprimary435/320.1
dc.subject.uspcother536/23.7
dc.date.filed1998-11-25
dc.publisher.digitalTexas A&M University. Libraries


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