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A novel protein refolding method using a zeolite.

Hiroyuki Chiku·Akiko Kawai·Toyotaka Ishibashi·Masahide Takehara·Takuro Yanai·Fujio Mizukami·Kengo Sakaguchi
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Abstract

We have succeeded in developing a simple and effective protein refolding method using the inorganic catalyst, beta-zeolite. The method involves the adsorption of proteins solubilized with 6M guanidine hydrochloride from inclusion body (IB) preparations onto the zeolite. The denaturant is then removed, and the proteins in the IBs are released from the zeolite with polyoxyethylene detergent and salt. All of the IBs tested (11 different species) were successfully refolded under these conditions. The refolded proteins are biochemically active, and NMR analysis of one of the proteins (replication protein A 8) supports the conclusion that correct refolding does occur. Based on these results, we discuss the refolding mechanism.

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AnimalsEscherichia coliGuanidineInclusion BodiesProtein FoldingRecombinant ProteinsReplication Protein AZeolitesJournal Article

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Hiroyuki Chiku, Akiko Kawai, Toyotaka Ishibashi, Masahide Takehara, Takuro Yanai, Fujio Mizukami, Kengo Sakaguchi. 2005-11-08. A novel protein refolding method using a zeolite.. https://doi.org/10.1016/j.ab.2005.10.032

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