Literature DB >> 14769332

Cell-free N-terminal protein labeling using initiator suppressor tRNA.

Sergey Mamaev1, Jerzy Olejnik, Edyta Krzymanska Olejnik, Kenneth J Rothschild.   

Abstract

A highly efficient method for the introduction of fluorophores and other markers at the N terminus of proteins produced in a cell-free extract has been developed. The method utilizes an amber (CUA) initiator suppressor tRNA chemically aminoacylated with a fluorophore-amino acid conjugate which is introduced into an Escherichia coli S30 cell-free translation system. The DNA template contains a complementary amber (UAG) codon instead of the normal initiation (AUG) codon. Using this approach, the fluorophore BODIPY-F1 (4,4-difluoro-5,7-dimethyl-4-bora-3a,4a- diaza-s-indacene-3-propionic acid) has been incorporated at the N terminus of several model proteins. The specific labeling achieved (27-67%) using this approach is much higher than that of wild-type tRNAs. Several potential biophysical and biotechnological applications of this new technology are described.

Entities:  

Mesh:

Substances:

Year:  2004        PMID: 14769332     DOI: 10.1016/j.ab.2003.11.002

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  11 in total

Review 1.  Hijacking Translation Initiation for Synthetic Biology.

Authors:  Jeffery M Tharp; Natalie Krahn; Umesh Varshney; Dieter Söll
Journal:  Chembiochem       Date:  2020-03-02       Impact factor: 3.164

2.  N-terminal protein modification using simple aminoacyl transferase substrates.

Authors:  Anne M Wagner; Mark W Fegley; John B Warner; Christina L J Grindley; Nicholas P Marotta; E James Petersson
Journal:  J Am Chem Soc       Date:  2011-09-06       Impact factor: 15.419

3.  Mutant methionyl-tRNA synthetase from bacteria enables site-selective N-terminal labeling of proteins expressed in mammalian cells.

Authors:  John T Ngo; Erin M Schuman; David A Tirrell
Journal:  Proc Natl Acad Sci U S A       Date:  2013-03-11       Impact factor: 11.205

4.  Photocleavage-based affinity purification and printing of cell-free expressed proteins: application to proteome microarrays.

Authors:  Mark Lim; Kenneth J Rothschild
Journal:  Anal Biochem       Date:  2008-08-12       Impact factor: 3.365

5.  Single-molecule imaging of a fluorescent unnatural amino acid incorporated into nicotinic receptors.

Authors:  Rigo Pantoja; Erik A Rodriguez; Mohammed I Dibas; Dennis A Dougherty; Henry A Lester
Journal:  Biophys J       Date:  2009-01       Impact factor: 4.033

Review 6.  Recent developments of engineered translational machineries for the incorporation of non-canonical amino acids into polypeptides.

Authors:  Naohiro Terasaka; Yoshihiko Iwane; Anna-Skrollan Geiermann; Yuki Goto; Hiroaki Suga
Journal:  Int J Mol Sci       Date:  2015-03-20       Impact factor: 5.923

7.  Highly chromophoric Cy5-methionine for N-terminal fluorescent tagging of proteins in eukaryotic translation systems.

Authors:  Jung Min Kim; Baik Lin Seong
Journal:  Sci Rep       Date:  2017-09-14       Impact factor: 4.379

Review 8.  Engineering Translation Components Improve Incorporation of Exotic Amino Acids.

Authors:  Takayuki Katoh; Hiroaki Suga
Journal:  Int J Mol Sci       Date:  2019-01-26       Impact factor: 5.923

Review 9.  Isotope-edited IR spectroscopy for the study of membrane proteins.

Authors:  Isaiah T Arkin
Journal:  Curr Opin Chem Biol       Date:  2006-08-28       Impact factor: 8.822

Review 10.  Protein microarrays: high-throughput tools for proteomics.

Authors:  Oda Stoevesandt; Michael J Taussig; Mingyue He
Journal:  Expert Rev Proteomics       Date:  2009-04       Impact factor: 3.940

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.