Literature DB >> 21365492

Construction of yeast surface-displayed cDNA libraries.

Scott Bidlingmaier1, Bin Liu.   

Abstract

Using yeast display, heterologous protein fragments can be efficiently displayed at high copy levels on the Saccharomyces cerevisiae cell wall. Yeast display can be used to screen large expressed protein libraries for proteins or protein fragments with specific binding properties. Recently, yeast surface-displayed cDNA libraries have been constructed and used to identify proteins that bind to various target molecules such as peptides, small molecules, and antibodies. Because yeast protein expression pathways are similar to those found in mammalian cells, human protein fragments displayed on the yeast cell wall are likely to be properly folded and functional. Coupled with fluorescence-activated cell sorting, yeast surface-displayed cDNA libraries potentially allow the selection of protein fragments or domains with affinity for any soluble molecule that can be fluorescently detected. In this report, we describe protocols for the construction and validation of yeast surface-displayed cDNA libraries using preexisting yeast two-hybrid cDNA libraries as a starting point.

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Year:  2011        PMID: 21365492      PMCID: PMC3228857          DOI: 10.1007/978-1-61779-065-2_13

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  16 in total

Review 1.  Direct selection of cDNAs from filamentous phage surface display libraries: potential and limitations.

Authors:  Claudio Rhyner; Rimantas Kodzius; Reto Crameri
Journal:  Curr Pharm Biotechnol       Date:  2002-03       Impact factor: 2.837

Review 2.  Direct selection of cDNAs by phage display.

Authors:  R Crameri; G Achatz; M Weichel; C Rhyner
Journal:  Methods Mol Biol       Date:  2002

3.  T7 phage display: a novel genetic selection system for cloning RNA-binding proteins from cDNA libraries.

Authors:  S Danner; J G Belasco
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-23       Impact factor: 11.205

4.  A tethered catalysis, two-hybrid system to identify protein-protein interactions requiring post-translational modifications.

Authors:  Dawei Guo; Tony R Hazbun; Xin-Jing Xu; Sze-Ling Ng; Stanley Fields; Min-Hao Kuo
Journal:  Nat Biotechnol       Date:  2004-06-20       Impact factor: 54.908

5.  Construction and application of a yeast surface-displayed human cDNA library to identify post-translational modification-dependent protein-protein interactions.

Authors:  Scott Bidlingmaier; Bin Liu
Journal:  Mol Cell Proteomics       Date:  2005-12-01       Impact factor: 5.911

Review 6.  The two-hybrid system: an assay for protein-protein interactions.

Authors:  S Fields; R Sternglanz
Journal:  Trends Genet       Date:  1994-08       Impact factor: 11.639

7.  Serological identification of breast cancer-related antigens from a Saccharomyces cerevisiae surface display library.

Authors:  Andreas Wadle; Axel Mischo; Jochen Imig; Beate Wüllner; Dan Hensel; Kristin Wätzig; Frank Neumann; Boris Kubuschok; Werner Schmidt; Lloyd J Old; Michael Pfreundschuh; Christoph Renner
Journal:  Int J Cancer       Date:  2005-10-20       Impact factor: 7.396

8.  Identification of MCAM/CD146 as the target antigen of a human monoclonal antibody that recognizes both epithelioid and sarcomatoid types of mesothelioma.

Authors:  Scott Bidlingmaier; Jiang He; Yong Wang; Feng An; Jinjin Feng; Dario Barbone; Dongwei Gao; Ben Franc; V Courtney Broaddus; Bin Liu
Journal:  Cancer Res       Date:  2009-02-03       Impact factor: 12.701

9.  Interrogating yeast surface-displayed human proteome to identify small molecule-binding proteins.

Authors:  Scott Bidlingmaier; Bin Liu
Journal:  Mol Cell Proteomics       Date:  2007-07-28       Impact factor: 5.911

10.  Selection of ligands by panning of domain libraries displayed on phage lambda reveals new potential partners of synaptojanin 1.

Authors:  A Zucconi; L Dente; E Santonico; L Castagnoli; G Cesareni
Journal:  J Mol Biol       Date:  2001-04-13       Impact factor: 5.469

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  8 in total

1.  Utilizing Yeast Surface Human Proteome Display Libraries to Identify Small Molecule-Protein Interactions.

Authors:  Scott Bidlingmaier; Bin Liu
Journal:  Methods Mol Biol       Date:  2015

2.  Combining Phage and Yeast Cell Surface Antibody Display to Identify Novel Cell Type-Selective Internalizing Human Monoclonal Antibodies.

Authors:  Scott Bidlingmaier; Yang Su; Bin Liu
Journal:  Methods Mol Biol       Date:  2015

Review 3.  Identification of Posttranslational Modification-Dependent Protein Interactions Using Yeast Surface Displayed Human Proteome Libraries.

Authors:  Scott Bidlingmaier; Bin Liu
Journal:  Methods Mol Biol       Date:  2015

Review 4.  Mosquito Saliva Reshapes Alphavirus Infection and Immunopathogenesis.

Authors:  Siew-Wai Fong; R Manjunatha Kini; Lisa F P Ng
Journal:  J Virol       Date:  2018-05-29       Impact factor: 5.103

5.  Proteome-wide Identification of Novel Ceramide-binding Proteins by Yeast Surface cDNA Display and Deep Sequencing.

Authors:  Scott Bidlingmaier; Kevin Ha; Nam-Kyung Lee; Yang Su; Bin Liu
Journal:  Mol Cell Proteomics       Date:  2016-01-04       Impact factor: 5.911

6.  Yeast surface display is a novel tool for the rapid immunological characterization of plant-derived food allergens.

Authors:  Milica Popovic; Radivoje Prodanovic; Raluca Ostafe; Stefan Schillberg; Rainer Fischer; Marija Gavrovic-Jankulovic
Journal:  Immunol Res       Date:  2015-03       Impact factor: 2.829

7.  Identification of Novel Protein-Ligand Interactions by Exon Microarray Analysis of Yeast Surface Displayed cDNA Library Selection Outputs.

Authors:  Scott Bidlingmaier; Bin Liu
Journal:  Methods Mol Biol       Date:  2015

8.  Yeast Surface Display: New Opportunities for a Time-Tested Protein Engineering System.

Authors:  Maryam Raeeszadeh-Sarmazdeh; Eric T Boder
Journal:  Methods Mol Biol       Date:  2022
  8 in total

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