Literature DB >> 16076456

Protein synthesis by pure translation systems.

Yoshihiro Shimizu1, Takashi Kanamori, Takuya Ueda.   

Abstract

We have developed a partially recombinant, cell-free, protein-synthesis system reconstituted solely from those essential elements of the Escherichia coli translation system, termed protein synthesis using recombinant elements (PURE). It provides higher reaction controllability in comparison to crude cell-free protein-synthesis systems for translation studies and biotechnology applications. The PURE system stands out among translation methods in that it provides not only a simple and unique "reverse" purification method of separating the synthesized protein from reaction mixture, but also that the system can be tailor-made according to individual protein requirements. In this paper, two new approaches to obtaining active proteins are described: the use of molecular chaperones, and modification of the reaction conditions. Several possible applications of the PURE system are also discussed.

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Year:  2005        PMID: 16076456     DOI: 10.1016/j.ymeth.2005.04.006

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


  96 in total

1.  Knot formation in newly translated proteins is spontaneous and accelerated by chaperonins.

Authors:  Anna L Mallam; Sophie E Jackson
Journal:  Nat Chem Biol       Date:  2011-12-18       Impact factor: 15.040

2.  The PURE system for the cell-free synthesis of membrane proteins.

Authors:  Yutetsu Kuruma; Takuya Ueda
Journal:  Nat Protoc       Date:  2015-08-13       Impact factor: 13.491

3.  Continued protein synthesis at low [ATP] and [GTP] enables cell adaptation during energy limitation.

Authors:  Michael C Jewett; Mark L Miller; Yvonne Chen; James R Swartz
Journal:  J Bacteriol       Date:  2008-11-21       Impact factor: 3.490

4.  Bimodal protein solubility distribution revealed by an aggregation analysis of the entire ensemble of Escherichia coli proteins.

Authors:  Tatsuya Niwa; Bei-Wen Ying; Katsuyo Saito; WenZhen Jin; Shoji Takada; Takuya Ueda; Hideki Taguchi
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-27       Impact factor: 11.205

5.  Bases in the anticodon loop of tRNA(Ala)(GGC) prevent misreading.

Authors:  Hiroshi Murakami; Atsushi Ohta; Hiroaki Suga
Journal:  Nat Struct Mol Biol       Date:  2009-03-22       Impact factor: 15.369

6.  Artificial cells: crowded genes perform differently.

Authors:  Friedrich C Simmel
Journal:  Nat Nanotechnol       Date:  2013-08       Impact factor: 39.213

Review 7.  Genome engineering.

Authors:  Peter A Carr; George M Church
Journal:  Nat Biotechnol       Date:  2009-12       Impact factor: 54.908

8.  Peptide release on the ribosome depends critically on the 2' OH of the peptidyl-tRNA substrate.

Authors:  Julie L Brunelle; Jeffrey J Shaw; Elaine M Youngman; Rachel Green
Journal:  RNA       Date:  2008-06-20       Impact factor: 4.942

9.  Cell-free expression and stable isotope labelling strategies for membrane proteins.

Authors:  Solmaz Sobhanifar; Sina Reckel; Friederike Junge; Daniel Schwarz; Lei Kai; Mikhail Karbyshev; Frank Löhr; Frank Bernhard; Volker Dötsch
Journal:  J Biomol NMR       Date:  2009-08-13       Impact factor: 2.835

10.  Evidence for context-dependent complementarity of non-Shine-Dalgarno ribosome binding sites to Escherichia coli rRNA.

Authors:  Pamela A Barendt; Najaf A Shah; Gregory A Barendt; Parth A Kothari; Casim A Sarkar
Journal:  ACS Chem Biol       Date:  2013-03-07       Impact factor: 5.100

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