Literature DB >> 11403575

Intein-mediated ligation and cyclization of expressed proteins.

M Q Xu1, T C Evans.   

Abstract

Protein splicing is a posttranslational processing event that releases an internal protein sequence from a protein precursor. During the splicing process the internal protein sequence, termed an intein, embedded in the protein precursor self-catalyzes its excision and the ligation of the flanking protein regions, termed exteins. The dissection of the splicing pathway, which involves the precise cleavage and formation of peptide bonds, and the identification of key catalytic residues at the splice junctions have led to the modulation of the protein splicing process as a protein engineering tool. Novel strategies have been developed to use intein-catalyzed reactions for the production and manipulation of proteins and peptides. These new approaches have broken down the size limitation barrier of chemical synthetic methods and are less technically demanding. The purpose of this article is to describe how to use self-splicing inteins in protein semisynthesis and backbone cyclization. The first two sections of the article provide a brief review of the distinct chemical steps that underlie protein splicing and intein enabled technology. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11403575     DOI: 10.1006/meth.2001.1187

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


  28 in total

1.  Phosphorylation of eIF4E attenuates its interaction with mRNA 5' cap analogs by electrostatic repulsion: intein-mediated protein ligation strategy to obtain phosphorylated protein.

Authors:  Joanna Zuberek; Aleksandra Wyslouch-Cieszynska; Anna Niedzwiecka; Michal Dadlez; Janusz Stepinski; Wojciech Augustyniak; Anne-Claude Gingras; Zhibo Zhang; Stephen K Burley; Nahum Sonenberg; Ryszard Stolarski; Edward Darzynkiewicz
Journal:  RNA       Date:  2003-01       Impact factor: 4.942

2.  N-terminal cysteinyl proteins can be prepared using thrombin cleavage.

Authors:  Dongsheng Liu; Rong Xu; Kaushik Dutta; David Cowburn
Journal:  FEBS Lett       Date:  2008-03-10       Impact factor: 4.124

3.  Recombinant chymosin used for exact and complete removal of a prochymosin derived fusion tag releasing intact native target protein.

Authors:  Sune F L Justesen; Kasper Lamberth; Lise-Lotte B Nielsen; Claus Schafer-Nielsen; Søren Buus
Journal:  Protein Sci       Date:  2009-05       Impact factor: 6.725

4.  A circularly permuted beta-lactamase as a novel reporter for evaluation of protein cyclization efficiency.

Authors:  Jeong Seon Kwon; Jyotiranjan Bal; Hai Min Hwang; Jeong-Yoon Kim
Journal:  J Microbiol       Date:  2008-08-31       Impact factor: 3.422

Review 5.  Recent advances in segmental isotope labeling of proteins: NMR applications to large proteins and glycoproteins.

Authors:  Lenka Skrisovska; Mario Schubert; Frédéric H-T Allain
Journal:  J Biomol NMR       Date:  2009-08-19       Impact factor: 2.835

6.  Controllable protein cleavages through intein fragment complementation.

Authors:  Gerrit Volkmann; Wenchang Sun; Xiang-Qin Liu
Journal:  Protein Sci       Date:  2009-11       Impact factor: 6.725

7.  Butelase 1 is an Asx-specific ligase enabling peptide macrocyclization and synthesis.

Authors:  Giang K T Nguyen; Shujing Wang; Yibo Qiu; Xinya Hemu; Yilong Lian; James P Tam
Journal:  Nat Chem Biol       Date:  2014-07-20       Impact factor: 15.040

8.  Microbial polyhydroxyalkanote synthesis repression protein PhaR as an affinity tag for recombinant protein purification.

Authors:  Shuang Zhang; Zhi Hui Wang; Guo Qiang Chen
Journal:  Microb Cell Fact       Date:  2010-05-10       Impact factor: 5.328

Review 9.  Inteins, valuable genetic elements in molecular biology and biotechnology.

Authors:  Skander Elleuche; Stefanie Pöggeler
Journal:  Appl Microbiol Biotechnol       Date:  2010-05-07       Impact factor: 4.813

10.  Expressed protein ligation using an N-terminal cysteine containing fragment generated in vivo from a pelB fusion protein.

Authors:  Paul S Hauser; Robert O Ryan
Journal:  Protein Expr Purif       Date:  2007-04-10       Impact factor: 1.650

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