Literature DB >> 15504701

Rapid translation system: a novel cell-free way from gene to protein.

Michael Hoffmann1, Cordula Nemetz, Kairat Madin, Bernd Buchberger.   

Abstract

Proteome research has recently been stimulated by important technological advances in the field of recombinant protein expression. One major breakthrough was the development of a new generation of cell-free transcription/translation systems. The open and flexible character of these systems allows direct control over expression conditions via the addition of supplements to the expression reaction. The possibility of working with linear expression templates instead of cloned plasmids and the ease of downstream processing, circumventing the need for cell-lysis, makes them ideally suited for high-throughput screening applications. Among these novel cell-free systems, the Rapid Translation System (RTS) developed by Roche is the first one that is scalable from micrograms to milligrams of protein. This review describes the basic principles of RTS which differentiate it from traditional in vitro expression technologies, starting from template generation to high-end applications like labeling for structural biology research. Recent results obtained by RTS users from different institutions are presented to illustrate each step of a novel cell-free protein expression workflow and its benefits compared to traditional cell-based expression.

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Year:  2004        PMID: 15504701     DOI: 10.1016/S1387-2656(04)10001-X

Source DB:  PubMed          Journal:  Biotechnol Annu Rev        ISSN: 1387-2656


  10 in total

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Journal:  Methods       Date:  2006-11       Impact factor: 3.608

2.  Cell-free expression and functionality analysis of the tobacco lectin.

Authors:  Gianni Vandenborre; Nausicaä Lannoo; Guy Smagghe; Erica Daniel; Andrew Breite; Thomas Soin; Linda Jacobsen; Els J M Van Damme
Journal:  In Vitro Cell Dev Biol Anim       Date:  2008-06-17       Impact factor: 2.416

3.  "System 48" high-throughput cloning and protein expression analysis.

Authors:  James M Abdullah; Andrzej Joachimiak; Frank R Collart
Journal:  Methods Mol Biol       Date:  2009

4.  The substrate recognition domains of the N-end rule pathway.

Authors:  Takafumi Tasaki; Adriana Zakrzewska; Drew D Dudgeon; Yonghua Jiang; John S Lazo; Yong Tae Kwon
Journal:  J Biol Chem       Date:  2008-11-13       Impact factor: 5.157

5.  Real-time assay for testing components of protein synthesis.

Authors:  Gabriel Rosenblum; Chunlai Chen; Jaskiran Kaur; Xiaonan Cui; Yale E Goldman; Barry S Cooperman
Journal:  Nucleic Acids Res       Date:  2012-03-14       Impact factor: 16.971

6.  Towards the construction of expressed proteomes using a Leishmania tarentolae based cell-free expression system.

Authors:  Oleksiy Kovtun; Sergey Mureev; Wayne Johnston; Kirill Alexandrov
Journal:  PLoS One       Date:  2010-12-21       Impact factor: 3.752

7.  Antibodies on demand: a fast method for the production of human scFvs with minimal amounts of antigen.

Authors:  Ingrid Babel; Rodrigo Barderas; Alberto Peláez-García; J Ignacio Casal
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8.  Use of pIVEX plasmids for protein overproduction in Escherichia coli.

Authors:  Julie Rogé; Jean-Michel Betton
Journal:  Microb Cell Fact       Date:  2005-06-02       Impact factor: 5.328

9.  Functional expression of a single-chain antibody to ErbB-2 in plants and cell-free systems.

Authors:  Patrizia Galeffi; Alessio Lombardi; Immacolata Pietraforte; Flavia Novelli; Monica Di Donato; Maria Sperandei; Andrea Tornambé; Rocco Fraioli; Aline Martayan; Pier Giorgio Natali; Maria Benevolo; Marcella Mottolese; Francisco Ylera; Cristina Cantale; Patrizio Giacomini
Journal:  J Transl Med       Date:  2006-09-29       Impact factor: 5.531

Review 10.  Bacterial cell-free expression technology to in vitro systems engineering and optimization.

Authors:  Filippo Caschera
Journal:  Synth Syst Biotechnol       Date:  2017-08-07
  10 in total

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