Literature DB >> 8125285

A T7 expression vector for producing N- and C-terminal fusion proteins with glutathione S-transferase.

A D Sharrocks1.   

Abstract

The pGEX system for protein production in E. coli is widely used in molecular biology. A bacterial expression vector, pETGEXCT, which incorporates features of the pGEX and pET expression systems was designed. pETGEXCT allows the production of N- and C-terminal fusions to glutathione S-transferase (GST) under the tight control of the T7 promoter. Use of this vector can circumvent problems associated with unstable or inactive fusions to the N terminus of GST. Indeed, it is demonstrated that fusions to the N terminus of the eukaryotic DNA-binding protein, RSRFC4, cannot be tolerated. Fusion of RSRFC4 to the N terminus of GST in the pETGEXCT vector is a prerequisite to purify the RSRFC4 DNA-binding domain in an active form using glutathione-agarose affinity chromatography.

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Year:  1994        PMID: 8125285     DOI: 10.1016/0378-1119(94)90789-7

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  32 in total

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Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

5.  Interaction of SNAREs with ArfGAPs precedes recruitment of Sec18p/NSF.

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Authors:  Marcus C S Lee; Pedro A Moura; Elizabeth A Miller; David A Fidock
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7.  Insights into the Clp/HSP100 chaperone system from chloroplasts of Arabidopsis thaliana.

Authors:  Germán L Rosano; Eduardo M Bruch; Eduardo A Ceccarelli
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8.  5-Hydroxymethylcytosine in E-box motifs ACAT|GTG and ACAC|GTG increases DNA-binding of the B-HLH transcription factor TCF4.

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Journal:  EMBO J       Date:  2004-09-30       Impact factor: 11.598

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