Literature DB >> 20204860

Ribosome display with the PURE technology.

Takuya Ueda1, Takashi Kanamori, Hiroyuki Ohashi.   

Abstract

The ribosome display utilizes the formation of the mRNA-ribosome-polypeptide ternary complex in the cell-free protein synthesis system as the linking of the genotype (mRNA) to the phenotype (polypeptide). However, the presence of intrinsic components such as nucleases in the cell-extract based cell-free protein synthesis systems inevitably reduces the stability of the ternary complex, which would prevent attainment of reliable results. We have developed an efficient and highly controllable ribosome display system using the Protein synthesis Using Recombinant Elements (PURE) system. The mRNA-ribosome-polypeptide ternary complex is highly stable in the PURE system and then the selected mRNA can be easily recovered, because activities of nucleases and other inhibitory factors are very low in the PURE system. Furthermore, omission of the release factors within the original PURE system can aid stalling of the ribosome at the termination codon to form the mRNA-ribosome-polypeptide ternary complex. We believe that these advantages assure the usability of the modified PURE system for ribosome display.

Mesh:

Substances:

Year:  2010        PMID: 20204860     DOI: 10.1007/978-1-60327-331-2_18

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


  8 in total

1.  Overview of cell-free protein synthesis: historic landmarks, commercial systems, and expanding applications.

Authors:  Shaorong Chong
Journal:  Curr Protoc Mol Biol       Date:  2014-10-01

2.  Streamlined protocol for mRNA display.

Authors:  Pamela A Barendt; Daphne T W Ng; Casey N McQuade; Casim A Sarkar
Journal:  ACS Comb Sci       Date:  2013-01-25       Impact factor: 3.784

Review 3.  Cell-free protein synthesis: the state of the art.

Authors:  James W Whittaker
Journal:  Biotechnol Lett       Date:  2012-10-21       Impact factor: 2.461

4.  Reconstitution of translation from Thermus thermophilus reveals a minimal set of components sufficient for protein synthesis at high temperatures and functional conservation of modern and ancient translation components.

Authors:  Ying Zhou; Haruichi Asahara; Eric A Gaucher; Shaorong Chong
Journal:  Nucleic Acids Res       Date:  2012-06-20       Impact factor: 16.971

5.  A highly scalable peptide-based assay system for proteomics.

Authors:  Igor A Kozlov; Elliot R Thomsen; Sarah E Munchel; Patricia Villegas; Petr Capek; Austin J Gower; Stephanie J K Pond; Eugene Chudin; Mark S Chee
Journal:  PLoS One       Date:  2012-06-12       Impact factor: 3.240

6.  Atomic mutagenesis of stop codon nucleotides reveals the chemical prerequisites for release factor-mediated peptide release.

Authors:  Thomas Philipp Hoernes; Nina Clementi; Michael Andreas Juen; Xinying Shi; Klaus Faserl; Jessica Willi; Catherina Gasser; Christoph Kreutz; Simpson Joseph; Herbert Lindner; Alexander Hüttenhofer; Matthias David Erlacher
Journal:  Proc Natl Acad Sci U S A       Date:  2018-01-03       Impact factor: 11.205

7.  Retrospective analysis of the preparation and application of immunotherapy in cancer treatment (Review).

Authors:  Jiachen Lu; Jianing Ding; Zhaoxia Liu; Tingtao Chen
Journal:  Int J Oncol       Date:  2022-01-04       Impact factor: 5.650

8.  Development of Next-Generation Peptide Binders Using In vitro Display Technologies and Their Potential Applications.

Authors:  Akira Wada
Journal:  Front Immunol       Date:  2013-08-01       Impact factor: 7.561

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.