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
Hauptverfasser: Hirano, Yoshinori, Gao, Yong-Guang, Simanshu, Dhirendra, Stephenson, Daniel, Vu, Ngoc, Malinina, Lucy, Chalfant, Charles, Pate, Dinshaw, Brown, Rhoderick
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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 )
ISSN:2331-8325
2331-8325
DOI:10.21769/BioProtoc.3906