Literature DB >> 11243841

Selection of RNA-binding peptides using mRNA-peptide fusions.

J E Barrick1, T T Takahashi, A Balakin, R W Roberts.   

Abstract

We have been working to apply in vitro selection to isolate novel RNA-binding peptides. To do this, we use mRNA-protein fusions, peptides covalently attached to their own mRNA. Here, we report selection protocols developed using the arginine-rich domain of bacteriophage lambda-N protein and its binding target, the boxB RNA. Systematic investigation of possible paths for a selection round has allowed us to design a reliable and efficient protocol to enrich RNA-binding peptides from nonfunctional members of a complex mixture. The protocols we have developed should greatly facilitate the isolation of new molecules using the fusion system.

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Year:  2001        PMID: 11243841     DOI: 10.1006/meth.2000.1139

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  12 in total

1.  Large libraries reveal diverse solutions to an RNA recognition problem.

Authors:  J E Barrick; T T Takahashi; J Ren; T Xia; R W Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-23       Impact factor: 11.205

2.  The RNA-protein complex: direct probing of the interfacial recognition dynamics and its correlation with biological functions.

Authors:  Tianbing Xia; Hans-Christian Becker; Chaozhi Wan; Adam Frankel; Richard W Roberts; Ahmed H Zewail
Journal:  Proc Natl Acad Sci U S A       Date:  2003-06-18       Impact factor: 11.205

3.  The RNA-binding domain of bacteriophage P22 N protein is highly mutable, and a single mutation relaxes specificity toward lambda.

Authors:  Alexis I Cocozaki; Ingrid R Ghattas; Colin A Smith
Journal:  J Bacteriol       Date:  2008-09-26       Impact factor: 3.490

4.  Sequence analysis of an artificial family of RNA-binding peptides.

Authors:  Jeffrey E Barrick; Richard W Roberts
Journal:  Protein Sci       Date:  2002-11       Impact factor: 6.725

5.  Directed Evolution of Glycopeptides Using mRNA Display.

Authors:  Satoru Horiya; Jennifer K Bailey; Isaac J Krauss
Journal:  Methods Enzymol       Date:  2017-08-18       Impact factor: 1.600

6.  Highly stable and efficient mRNA templates for mRNA-protein fusions and C-terminally labeled proteins.

Authors:  Etsuko Miyamoto-Sato; Hideaki Takashima; Shinichiro Fuse; Kaori Sue; Masamichi Ishizaka; Seiji Tateyama; Kenichi Horisawa; Tatsuya Sawasaki; Yaeta Endo; Hiroshi Yanagawa
Journal:  Nucleic Acids Res       Date:  2003-08-01       Impact factor: 16.971

7.  Synthesis of HIV-1 Psi-site RNA sequences with site specific incorporation of the fluorescent base analog 2-aminopurine.

Authors:  Chang Zhao; John P Marino
Journal:  Tetrahedron       Date:  2007-04-23       Impact factor: 2.457

Review 8.  Directing evolution of novel ligands by mRNA display.

Authors:  Golnaz Kamalinia; Brian J Grindel; Terry T Takahashi; Steven W Millward; Richard W Roberts
Journal:  Chem Soc Rev       Date:  2021-06-24       Impact factor: 60.615

9.  The effect of RNA base lesions on mRNA translation.

Authors:  Alessandro Calabretta; Pascal A Küpfer; Christian J Leumann
Journal:  Nucleic Acids Res       Date:  2015-04-20       Impact factor: 16.971

10.  An Efficient Ligation Method in the Making of an in vitro Virus for in vitro Protein Evolution.

Authors:  Ichiro Tabuchi; Sayaka Soramoto; Miho Suzuki; Koichi Nishigaki; Naoto Nemoto; Yuzuru Husimi
Journal:  Biol Proced Online       Date:  2002-10-28       Impact factor: 3.244

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