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Staphylococcal surface display in combinatorial protein engineering and epitope mapping of antibodies
KTH, Skolan för bioteknologi (BIO), Molekylär Bioteknologi.
KTH, Skolan för bioteknologi (BIO), Molekylär Bioteknologi.ORCID-id: 0000-0003-1763-9073
KTH, Skolan för bioteknologi (BIO), Proteomik.ORCID-id: 0000-0002-9977-5724
KTH, Skolan för bioteknologi (BIO), Proteomik.
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2010 (Engelska)Ingår i: Recent Patents on Biotechnology, ISSN 1872-2083, Vol. 4, nr 3, s. 171-182Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

The field of combinatorial protein engineering for generation of new affinity proteins started in the mid 80s by the development of phage display. Although phage display is a prime example of a simple yet highly efficient method, manifested by still being the standard technique 25 years later, new alternative technologies are available today. One of the more successful new display technologies is cell display. Here we review the field of cell display for directed evolution purposes, with focus on a recently developed method employing Gram-positive staphylococci as display host. Patents on the most commonly used cell display systems and on different modifications as well as specific applications of these systems are also included. General strategies for selection of new affinity proteins from cell-displayed libraries are discussed, with detailed examples mainly from studies on the staphylococcal display system. In addition, strategies for characterization of recombinant proteins on the staphylococcal cell surface, with an emphasis on an approach for epitope mapping of antibodies, are included.

Ort, förlag, år, upplaga, sidor
Bentham eBooks, 2010. Vol. 4, nr 3, s. 171-182
Nyckelord [en]
Affibody molecules, Antibody engineering, Bacterial display, Cell surface display, Combinatorial protein engineering, Epitope mapping, Staphylococcal surface display, Yeast display
Nationell ämneskategori
Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)
Identifikatorer
URN: urn:nbn:se:kth:diva-60005DOI: 10.2174/187220810793611536PubMedID: 21171954Scopus ID: 2-s2.0-78650001663OAI: oai:DiVA.org:kth-60005DiVA, id: diva2:477062
Anmärkning
QC 20120113Tillgänglig från: 2012-01-12 Skapad: 2012-01-12 Senast uppdaterad: 2012-01-13Bibliografiskt granskad

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Malm, MagdalenaUhlén, MathiasStåhl, StefanLöfblom, John

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Kronqvist, NinaMalm, MagdalenaRockberg, JohanHjelm, BarbaraUhlén, MathiasStåhl, StefanLöfblom, John
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Molekylär BioteknologiProteomik
Medicinsk bioteknologi (med inriktning mot cellbiologi (inklusive stamcellsbiologi), molekylärbiologi, mikrobiologi, biokemi eller biofarmaci)

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