Sorting a Staphylococcus aureus phage display library against ex vivo biomaterial

Department of Microbiology, Swedish University of Agricultural Sciences, SE-750 07 Uppsala, Sweden Correspondence Lars Frykberg lars.frykberg{at}mikrob.slu.se Received February 18, 2004 Accepted June 25, 2004 A phage display library made from Staphylococcus aureus DNA was sorted against a central ve...

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Veröffentlicht in:Journal of medical microbiology 2004-10, Vol.53 (10), p.945-951
Hauptverfasser: Bjerketorp, Joakim, Rosander, Anna, Nilsson, Martin, Jacobsson, Karin, Frykberg, Lars
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container_end_page 951
container_issue 10
container_start_page 945
container_title Journal of medical microbiology
container_volume 53
creator Bjerketorp, Joakim
Rosander, Anna
Nilsson, Martin
Jacobsson, Karin
Frykberg, Lars
description Department of Microbiology, Swedish University of Agricultural Sciences, SE-750 07 Uppsala, Sweden Correspondence Lars Frykberg lars.frykberg{at}mikrob.slu.se Received February 18, 2004 Accepted June 25, 2004 A phage display library made from Staphylococcus aureus DNA was sorted against a central venous catheter (CVC) that had been removed from a patient 2 days after insertion. After the first panning, approximately 50 % of the clones encoded proteins known to interact with mammalian proteins. After the second and third pannings, fibrinogen-binding and ß 2 -glycoprotein I (ß 2 -GPI)-binding phage particles were clearly dominating. Proteins adsorbed to different CVCs were investigated using specific antibodies. Among the proteins probed for, fibrinogen was most abundant, but, interestingly, ß 2 -GPI was also detected on all tested CVCs. Abbreviations: CF, clumping factor; CVC, central venous catheter; Fg, fibrinogen; Fn, fibronectin; ß 2 -GPI, ß 2 -glycoprotein I.
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After the first panning, approximately 50 % of the clones encoded proteins known to interact with mammalian proteins. After the second and third pannings, fibrinogen-binding and ß 2 -glycoprotein I (ß 2 -GPI)-binding phage particles were clearly dominating. Proteins adsorbed to different CVCs were investigated using specific antibodies. Among the proteins probed for, fibrinogen was most abundant, but, interestingly, ß 2 -GPI was also detected on all tested CVCs. 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After the first panning, approximately 50 % of the clones encoded proteins known to interact with mammalian proteins. After the second and third pannings, fibrinogen-binding and ß 2 -glycoprotein I (ß 2 -GPI)-binding phage particles were clearly dominating. Proteins adsorbed to different CVCs were investigated using specific antibodies. Among the proteins probed for, fibrinogen was most abundant, but, interestingly, ß 2 -GPI was also detected on all tested CVCs. 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source MEDLINE; Microbiology Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Bacterial Adhesion
Bacterial Proteins - metabolism
Bacteriology
beta 2-Glycoprotein I
Biocompatible Materials
Biological and medical sciences
Carrier Proteins - metabolism
Catheterization, Central Venous
Fibrinogen - metabolism
Fundamental and applied biological sciences. Psychology
Glycoproteins - metabolism
Infectious diseases
Medical sciences
Microbiology
Miscellaneous
Peptide Library
Protein Binding
Staphylococcus aureus
Staphylococcus aureus - genetics
Staphylococcus aureus - physiology
title Sorting a Staphylococcus aureus phage display library against ex vivo biomaterial
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