| Literature DB >> 25615978 |
Andreas Naschberger1, Barbara G Fürnrohr1, Theresia Dunzendorfer-Matt1, Christopher A Bonagura2, David Wright2, Klaus Scheffzek1, Bernhard Rupp3.
Abstract
The protease in the commonly used commercial low-foam enzyme cleaner Zymit cannot be completely blocked by EDTA, a widely used inhibitor of metalloproteases, at concentrations of up to 5 mM. Severe protein degradation was observed in crystallization drops after EDTA-containing wash steps unless residual Zymit protease was removed with NaOH at a concentration of at least 0.1 M. Wash steps with 0.1% SDS were also ineffective in completely removing the remaining Zymit activity. Protocols including wash steps with at least 0.1 M NaOH, as for example specified in the original ZENM protocol, are recommended to completely deactivate Zymit protease activity.Entities:
Keywords: Zymit; cleaning protocol; crystallization robotics; protease; protease inhibitor
Mesh:
Substances:
Year: 2015 PMID: 25615978 PMCID: PMC4304757 DOI: 10.1107/S2053230X14026053
Source DB: PubMed Journal: Acta Crystallogr F Struct Biol Commun ISSN: 2053-230X Impact factor: 1.056