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  2. Phage display - Wikipedia

    en.wikipedia.org/wiki/Phage_display

    Phage display is also a widely used method for in vitro protein evolution (also called protein engineering). As such, phage display is a useful tool in drug discovery. It is used for finding new ligands (enzyme inhibitors, receptor agonists and antagonists) to target proteins.

  3. Phage monographs - Wikipedia

    en.wikipedia.org/wiki/Phage_monographs

    The 'Nuts and Bolts' of Phage Therapy. a special issue of the journal, Current Pharmaceutical Biotechnology, consisting of six articles on phage therapy, plus an editorial. Carnazza, S., Guglielmino, S. eds. 2010. Phage Display As a Tool for Synthetic Biology. Nova Science Publishers, Hauppauge, New York. ISBN 978-1-60876-987-2, Google Books

  4. John McCafferty - Wikipedia

    en.wikipedia.org/wiki/John_McCafferty

    John McCafferty is a British scientist, one of the founders of Cambridge Antibody Technology alongside Sir Gregory Winter and David Chiswell. He is well known as one of the inventors of scFv antibody fragment phage display, [1] a technology that revolutionised the monoclonal antibody drug discovery.

  5. MorphoSys - Wikipedia

    en.wikipedia.org/wiki/MorphoSys

    MorphoSys’ main technology is HuCAL (Human Combinatorial Antibody Library), which is a collection of more than ten billion fully human antibodies in the form of a phage display bank and a system for their optimization. [27] Another technology recently developed is the OkapY bispecific antibody technology.

  6. Protein engineering - Wikipedia

    en.wikipedia.org/wiki/Protein_engineering

    Phage display methods are one option for screening proteins. This method involves the fusion of genes encoding the variant polypeptides with phage coat protein genes. Protein variants expressed on phage surfaces are selected by binding with immobilized targets in vitro.

  7. Biopanning - Wikipedia

    en.wikipedia.org/wiki/Biopanning

    The first step is to have phage display libraries prepared. This involves inserting foreign desired gene segments into a region of the bacteriophage genome, so that the peptide product will be displayed on the surface of the bacteriophage virion. The most often used are genes pIII or pVIII of bacteriophage M13. [5]

  8. George Smith (chemist) - Wikipedia

    en.wikipedia.org/wiki/George_Smith_(chemist)

    Smith first described the technique in 1985 when he displayed peptides on filamentous phage by fusing the peptide of interest onto gene III of filamentous phage. [8] He was awarded the 2018 Nobel Prize in Chemistry for this work, sharing his prize with Greg Winter and Frances Arnold.

  9. Cambridge Antibody Technology - Wikipedia

    en.wikipedia.org/wiki/Cambridge_Antibody_Technology

    Cambridge Antibody Technology Group Plc, (commonly referred to as CAT) was a biotechnology company headquartered in Cambridge, England, United Kingdom.Its core focus was on antibody therapeutics, primarily using Phage Display and Ribosome Display technology.