Purification of Cytosolic Phospholipase A2α C2-domain after Expression in Soluble Form in Escherichia coli
Previous expression/purification strategies for cytosolic phospholipase A 2 α C2-domain in Escherichia coli have relied on refolded protein recovered from inclusion bodies and sometimes containing C-terminal Cys139Ala and Cys141Ser substitutions to eliminate potential refolding complications induced...
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Veröffentlicht in: | Bio-protocol 2021-02, Vol.11 (3), p.e3906-e3906 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Previous expression/purification strategies for cytosolic phospholipase A
2
α C2-domain in
Escherichia coli
have relied on refolded protein recovered from inclusion bodies and sometimes containing C-terminal Cys139Ala and Cys141Ser substitutions to eliminate potential refolding complications induced by Cys residues. The protocol presented herein describes an effective method for the expression of cytosolic phospholipase A
2
α C2-domain in soluble form in
E. coli
and subsequent purification to homogeneity. This protocol, which utilizes a cleavable 6xHis-SUMO tag, has recently been used to gain insights into the structural basis of phosphatidylcholine recognition by the C2-domain of cytosolic phospholipase A
2
α (
Hirano
et al.
, 2019
) |
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ISSN: | 2331-8325 2331-8325 |
DOI: | 10.21769/BioProtoc.3906 |