Literature DB >> 10350066

Comparison of Escherichia coli and rabbit reticulocyte ribosome display systems.

J Hanes1, L Jermutus, C Schaffitzel, A Plückthun.   

Abstract

Ribosome display is a technology for library selection and simultaneous molecular evolution in vitro. We present here a comparison between an optimized Escherichia coli system and different rabbit reticulocyte ribosome display systems, optimized in a number of parameters, as a coupled eukaryotic system had been suggested to result in high enrichment factors [He and Taussig (1997) Nucleic Acids Res. 25, 5132-5134]. With all systems, antibody scFv fragments, complexed to the ribosomes and the corresponding mRNA, were enriched by binding to their cognate antigen and enrichment was always dependent on the absence of a stop codon and the presence of cognate antigen. However, the efficiency of the E. coli ribosome display system was 100-fold higher than an optimized uncoupled rabbit reticulocyte ribosome display system, with separate in vitro transcription and translation, which was in turn several-fold more efficient than the reported coupled system. Neither the E. coli nor the rabbit reticulocyte ribosome display system was dependent on the orientation of the domains of an antibody scFv fragment or on the spacer sequence. In summary, we could not detect any intrinsic advantage of using a eukaryotic translation system for ribosome display.

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Year:  1999        PMID: 10350066     DOI: 10.1016/s0014-5793(99)00475-5

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  9 in total

1.  Unbinding forces of single antibody-antigen complexes correlate with their thermal dissociation rates.

Authors:  F Schwesinger; R Ros; T Strunz; D Anselmetti; H J Güntherodt; A Honegger; L Jermutus; L Tiefenauer; A Pluckthun
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-29       Impact factor: 11.205

2.  Effects on RNAi of the tight structure, sequence and position of the targeted region.

Authors:  Koichi Yoshinari; Makoto Miyagishi; Kazunari Taira
Journal:  Nucleic Acids Res       Date:  2004-02-03       Impact factor: 16.971

3.  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

4.  A Cell-free Expression Pipeline for the Generation and Functional Characterization of Nanobodies.

Authors:  Lisa Haueis; Marlitt Stech; Stefan Kubick
Journal:  Front Bioeng Biotechnol       Date:  2022-04-28

5.  Tailoring in vitro evolution for protein affinity or stability.

Authors:  L Jermutus; A Honegger; F Schwesinger; J Hanes; A Plückthun
Journal:  Proc Natl Acad Sci U S A       Date:  2001-01-02       Impact factor: 11.205

6.  Characterization of Anti-Citrinin Specific ScFvs Selected from Non-Immunized Mouse Splenocytes by Eukaryotic Ribosome Display.

Authors:  Haiwei Cheng; Yifei Chen; Yi Yang; Xueqiu Chen; Xiaolu Guo; Aifang Du
Journal:  PLoS One       Date:  2015-07-01       Impact factor: 3.240

Review 7.  Ribosome Display Technology: Applications in Disease Diagnosis and Control.

Authors:  Adinarayana Kunamneni; Christian Ogaugwu; Steven Bradfute; Ravi Durvasula
Journal:  Antibodies (Basel)       Date:  2020-06-27

8.  RNA mutagenesis yields highly diverse mRNA libraries for in vitro protein evolution.

Authors:  George Kopsidas; Rachael K Carman; Emma L Stutt; Anna Raicevic; Anthony S Roberts; Mary-Anne V Siomos; Nada Dobric; Luisa Pontes-Braz; Greg Coia
Journal:  BMC Biotechnol       Date:  2007-04-11       Impact factor: 2.563

9.  Selection of anti-sulfadimidine specific ScFvs from a hybridoma cell by eukaryotic ribosome display.

Authors:  Yonghua Qi; Congming Wu; Suxia Zhang; Zhanhui Wang; Siyang Huang; Lei Dai; Shaochen Wang; Lining Xia; Kai Wen; Xingyuan Cao; Yongning Wu; Jianzhong Shen
Journal:  PLoS One       Date:  2009-07-29       Impact factor: 3.240

  9 in total

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