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2000
Volume 22, Issue 3
  • ISSN: 0929-8665
  • E-ISSN: 1875-5305

Abstract

Proline cis-trans isomerization plays a key role in the rate-determining steps of protein folding, and many different peptide-proline cis-trans isomerases (PPIases) catalyze this reaction. The acceleration of isomerization would be beneficial for in vitro refolding of protein preparations for industrial and research purposes. So we analyzed whether low-molecular-weight compounds that have been reported to enhance protein refolding have the activity to accelerate the isomerization. To evaluate the effects of chemicals on the isomerization rate, we set up a new NMR (EXSY) method that is invulnerable to their inhibitory activity, if any, and to their large NMR signals. With this method, we found that dimethylbenzylammonium propane sulfonate (NDSB-256) increase the isomerization rate in a concentration-dependent manner for the first time. Acceleration by imidazole (suggested but not experimentally confirmed) was also demonstrated. Arginine, a most popular refolding additive, did not show any significant effects on the isomerization reaction as expected.

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/content/journals/ppl/10.2174/0929866521666141124103904
2015-03-01
2025-05-11
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  • Article Type:
    Research Article
Keyword(s): Cis-trans isomerization; COS; EXSY; glycylproline; imidazole; NDSB; proline; refolding additive
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