Literature DB >> 12633996

mRNA display: ligand discovery, interaction analysis and beyond.

Terry T Takahashi1, Ryan J Austin, Richard W Roberts.   

Abstract

In vitro peptide and protein selection using mRNA display enables the discovery and directed evolution of new molecules from combinatorial libraries. These selected molecules can serve as tools to control and understand biological processes, enhance our understanding of molecular interactions and potentially treat disease in therapeutic applications. In mRNA display, mRNA molecules are covalently attached to the peptide or protein they encode. These mRNA-protein fusions enable in vitro selection of peptide and protein libraries of >10(13) different sequences. mRNA display has been used to discover novel peptide and protein ligands for RNA, small molecules and proteins, as well as to define cellular interaction partners of proteins and drugs. In addition, several unique applications are possible with mRNA display, including self-assembling protein chips and library construction with unnatural amino acids and chemically modified peptides.

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Year:  2003        PMID: 12633996     DOI: 10.1016/S0968-0004(03)00036-7

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  38 in total

1.  mRNA Display Discovery of a Novel Programmed Death Ligand 1 (PD-L1) Binding Peptide (a Peptide Ligand for PD-L1).

Authors:  Golnaz Kamalinia; Brian J Engel; Anupallavi Srinivasamani; Brian J Grindel; Justin N Ong; Michael A Curran; Terry T Takahashi; Steven W Millward; Richard W Roberts
Journal:  ACS Chem Biol       Date:  2020-04-30       Impact factor: 5.100

2.  In vitro selection of Jun-associated proteins using mRNA display.

Authors:  Kenichi Horisawa; Seiji Tateyama; Masamichi Ishizaka; Nobutaka Matsumura; Hideaki Takashima; Etsuko Miyamoto-Sato; Nobuhide Doi; Hiroshi Yanagawa
Journal:  Nucleic Acids Res       Date:  2004-12-02       Impact factor: 16.971

3.  Consolidating critical binding determinants by noncyclic rearrangement of protein secondary structure.

Authors:  Ramon K Tabtiang; Brent O Cezairliyan; Robert A Grant; Jesse C Cochrane; Robert T Sauer
Journal:  Proc Natl Acad Sci U S A       Date:  2005-02-02       Impact factor: 11.205

4.  Turning G proteins on and off using peptide ligands.

Authors:  William W Ja; Ofer Wiser; Ryan J Austin; Lily Y Jan; Richard W Roberts
Journal:  ACS Chem Biol       Date:  2006-10-24       Impact factor: 5.100

5.  Design, expression, and stability of a diverse protein library based on the human fibronectin type III domain.

Authors:  C Anders Olson; Richard W Roberts
Journal:  Protein Sci       Date:  2007-03       Impact factor: 6.725

6.  mRNA display for the selection and evolution of enzymes from in vitro-translated protein libraries.

Authors:  Burckhard Seelig
Journal:  Nat Protoc       Date:  2011-03-31       Impact factor: 13.491

Review 7.  Nucleic Acid-Barcoding Technologies: Converting DNA Sequencing into a Broad-Spectrum Molecular Counter.

Authors:  Glen Liszczak; Tom W Muir
Journal:  Angew Chem Int Ed Engl       Date:  2019-02-06       Impact factor: 15.336

Review 8.  Synthetic, Switchable Enzymes.

Authors:  Vic Norris; Sergey N Krylov; Pratul K Agarwal; Glenn J White
Journal:  J Mol Microbiol Biotechnol       Date:  2017-04-28

9.  Translation of DNA into a library of 13,000 synthetic small-molecule macrocycles suitable for in vitro selection.

Authors:  Brian N Tse; Thomas M Snyder; Yinghua Shen; David R Liu
Journal:  J Am Chem Soc       Date:  2008-10-29       Impact factor: 15.419

10.  Identification of novel SHPS-1-associated proteins and their roles in regulation of insulin-like growth factor-dependent responses in vascular smooth muscle cells.

Authors:  Xinchun Shen; Gang Xi; Yashwanth Radhakrishnan; David R Clemmons
Journal:  Mol Cell Proteomics       Date:  2009-03-18       Impact factor: 5.911

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