Besides detergents and I do not know what secret ingredients, the mixture includes *two* proteolytic enzymes.

If I were to design the mixture for needle cleaning, to digest different types of proteins, I would probably not use a costly enzyme with high substrate specificity, I would use proteases as found in washing powders such as savinase and neutrase (metalloenzyme) or any other combination of two out of six enzymes as offered by Novo Nordisk......


Jeroen


Am 09.09.19 um 00:01 schrieb Jorg Stetefeld:

Hi everyone,


this is Joerg Stetefeld.


I would like to approach the community in a peculiar case of a specific proteolytic cleavage during crystallization attempts.

Performing several crystallization screens we figured out that ZYMIT (https://www.ipcol.com/cleaners/zymit-low-foam) is the reason for a highly specific, but undesireable cleavage of protein components in our setups. Most remarkably, the cleavage site of our crystallisation target is not described in any protease database, and is highly inaccessible.



According to a publication by Naschberger /et al/, 2014 (doi:10.1107/S2053230X14026053) the authors very nicely describe the phenomenon. They also describe a very elegant protease removal protocol, which works in our hands very well.

At this point, however, I would like to know what is “behind” ZYMIT? Naschberger /et al/ say “Zymit contains an unspecified‘protease enzyme’ as a trade secret (http://www.ipcol.com/pdfs/Zymit_msds.pdf)”.


Does anyone has more insight into the secrets of ZYMIT? Our attempts to contact several vendors here in Canada/ abroad failed and a further characterisation of its nature would help us to understand this particular phenomenon of proteolytic cleavage.



Thank you very much in advance- Your advise is appreciated.


js





Jörg Stetefeld


**

<https://stetefeldlab.ca/>https://stetefeldlab.ca/<https://stetefeldlab.ca/>



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*Dr.math. et dis. nat.Jeroen R. Mesters*
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