Literature DB >> 9882572

Green fluorescent protein purification by organic extraction.

A V Yakhnin1, L M Vinokurov, A K Surin, Y B Alakhov.   

Abstract

Green fluorescent protein (GFP) is widely used as an excellent reporter molecule in biochemistry and cell biology. Some biochemical and immunological assays require high-purity GFP. However, the majority of current procedures for GFP purification include multiple time-consuming chromatography steps with a low yield of the desired product or require tag-containing proteins. An alternative method is described for the GFP purification without affinity extensions using organic extraction yielding a highly homogeneous protein indistinguishable in spectroscopic properties from that purified by previous methods. Copyright 1998 Academic Press.

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Year:  1998        PMID: 9882572     DOI: 10.1006/prep.1998.0981

Source DB:  PubMed          Journal:  Protein Expr Purif        ISSN: 1046-5928            Impact factor:   1.650


  19 in total

1.  Protein binding and unfolding by the chaperone ClpA and degradation by the protease ClpAP.

Authors:  J R Hoskins; S K Singh; M R Maurizi; S Wickner
Journal:  Proc Natl Acad Sci U S A       Date:  2000-08-01       Impact factor: 11.205

2.  Overlapping recognition determinants within the ssrA degradation tag allow modulation of proteolysis.

Authors:  J M Flynn; I Levchenko; M Seidel; S H Wickner; R T Sauer; T A Baker
Journal:  Proc Natl Acad Sci U S A       Date:  2001-09-04       Impact factor: 11.205

3.  SspB delivery of substrates for ClpXP proteolysis probed by the design of improved degradation tags.

Authors:  Greg L Hersch; Tania A Baker; Robert T Sauer
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-05       Impact factor: 11.205

4.  Ultra-high expression of a thermally responsive recombinant fusion protein in E. coli.

Authors:  Dominic C Chow; Matthew R Dreher; Kimberly Trabbic-Carlson; Ashutosh Chilkoti
Journal:  Biotechnol Prog       Date:  2006 May-Jun

5.  Versatile modes of peptide recognition by the ClpX N domain mediate alternative adaptor-binding specificities in different bacterial species.

Authors:  Tahmeena Chowdhury; Peter Chien; Shamsah Ebrahim; Robert T Sauer; Tania A Baker
Journal:  Protein Sci       Date:  2010-02       Impact factor: 6.725

6.  Chemoenzymatic reversible immobilization and labeling of proteins without prior purification.

Authors:  Mohammad Rashidian; James M Song; Rachel E Pricer; Mark D Distefano
Journal:  J Am Chem Soc       Date:  2012-05-08       Impact factor: 15.419

7.  A novel fluorescent protein-based biosensor for gram-negative bacteria.

Authors:  Yan Y Goh; Bow Ho; Jeak L Ding
Journal:  Appl Environ Microbiol       Date:  2002-12       Impact factor: 4.792

8.  Slippery substrates impair function of a bacterial protease ATPase by unbalancing translocation versus exit.

Authors:  Priscilla Hiu-Mei Too; Jenny Erales; Joana Danica Simen; Antonija Marjanovic; Philip Coffino
Journal:  J Biol Chem       Date:  2013-03-25       Impact factor: 5.157

9.  An Arabidopsis homologue of bacterial RecA that complements an E. coli recA deletion is targeted to plant mitochondria.

Authors:  F R Khazi; A C Edmondson; B L Nielsen
Journal:  Mol Genet Genomics       Date:  2003-05-24       Impact factor: 3.291

10.  Species-independent translational leaders facilitate cell-free expression.

Authors:  Sergei Mureev; Oleksiy Kovtun; Uyen T T Nguyen; Kirill Alexandrov
Journal:  Nat Biotechnol       Date:  2009-08-02       Impact factor: 54.908

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