pC6-2/caspase-6 system to purify glutathione-S-transferase-free recombinant fusion proteins expressed in Escherichia coli. (Q53554762)

15 May 2018

title

pC6-2/caspase-6 system to purify glutathione-S-transferase-free recombinant fusion proteins expressed in Escherichia coli. (English)

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15 May 2018

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Prabhat Kumar Purbey

1

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15 May 2018

P Cyril Jayakumar

series ordinal

2

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15 May 2018

Milind S Patole

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3

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15 May 2018

Sanjeev Galande

series ordinal

4

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15 May 2018

publication date

1 January 2006

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15 May 2018

published in

Nature Protocols

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15 May 2018

volume

1

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15 May 2018

issue

4

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15 May 2018

page(s)

1820-1827

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15 May 2018

https://scigraph.springernature.com/pub.10.1038/nprot.2006.310

exact match

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cites work

Caspases and apoptosis

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A novel DNA-binding motif in the nuclear matrix attachment DNA-binding protein SATB1

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Single-step purification of polypeptides expressed in Escherichia coli as fusions with glutathione S-transferase

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The conserved residue tyrosine 34 is essential for maximal activity of iron-superoxide dismutase from Escherichia coli.

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A critical review of the methods for cleavage of fusion proteins with thrombin and factor Xa.

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Eukaryotic proteins expressed in Escherichia coli: An improved thrombin cleavage and purification procedure of fusion proteins with glutathione S-transferase

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Caspases: preparation and characterization

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SATB1 cleavage by caspase 6 disrupts PDZ domain-mediated dimerization, causing detachment from chromatin early in T-cell apoptosis

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GST fusion vector with caspase-6 cleavage site for removal of fusion tag during column purification

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An atypical homeodomain in SATB1 promotes specific recognition of the key structural element in a matrix attachment region

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Novel protein purification system utilizing an N-terminal fusion protein and a caspase-3 cleavable linker

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A tissue-specific MAR/SAR DNA-binding protein with unusual binding site recognition

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Artificial chaperone-assisted refolding of denatured-reduced lysozyme: modulation of the competition between renaturation and aggregation

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Overproduction and purification of sigma 32, the Escherichia coli heat shock transcription factor.

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Caspase processing and nuclear export of CTP:phosphocholine cytidylyltransferase alpha during farnesol-induced apoptosis

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Transcription factor AP-2alpha is preferentially cleaved by caspase 6 and degraded by proteasome during tumor necrosis factor alpha-induced apoptosis in breast cancer cells

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The viral nucleocapsid protein of transmissible gastroenteritis coronavirus (TGEV) is cleaved by caspase-6 and -7 during TGEV-induced apoptosis

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Caspase-6 gene disruption reveals a requirement for lamin A cleavage in apoptotic chromatin condensation

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Cleavage at the caspase-6 site is required for neuronal dysfunction and degeneration due to mutant huntingtin

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Caspase-mediated degradation of human 5-lipoxygenase in B lymphocytic cells

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Breaking the connection: caspase 6 disconnects intermediate filament-binding domain of periplakin from its actin-binding N-terminal region

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Notch1 antiapoptotic activity is abrogated by caspase cleavage in dying T lymphocytes.

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Early N-terminal changes and caspase-6 cleavage of tau in Alzheimer's disease.

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Caspase-6 mediated cleavage of guanylate cyclase alpha 1 during deoxycholate-induced apoptosis: protective role of the nitric oxide signaling module

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Caspase proteolysis of desmin produces a dominant-negative inhibitor of intermediate filaments and promotes apoptosis

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31 March 2020

Identifiers

DOI

10.1038/NPROT.2006.310

1 reference

15 May 2018

Dimensions Publication ID

1010107514

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1 reference

15 May 2018