Hi Gloria,

Both can be made very easily in E.coli.
Both are active at 4°C, but especially 3C, I think.

I have plasmids for both somewhere in the freezer (you might find someone 
closer to you who can send HRV3C, but if you cannot, let me know off list).

I don't see any particular benefit of one over the other, but having both in 
your freezer means you can cleave off tags sequentially as needed by your 
purification strategies.

HTH,

Dave


Dr David C. Briggs CSci MRSB

Principal Laboratory Research Scientist

Signalling and Structural Biology Lab

The Francis Crick Institute

London, UK

==

about.me/david_briggs<http://about.me/david_briggs>

________________________________
From: CCP4 bulletin board <CCP4BB@JISCMAIL.AC.UK> on behalf of Gloria Borgstahl 
<gborgst...@gmail.com>
Sent: Wednesday, 7 December 2022, 20:26
To: CCP4BB@JISCMAIL.AC.UK <CCP4BB@JISCMAIL.AC.UK>
Subject: [ccp4bb] TEV vs HRV3C


External Sender: Use caution.

Hello my fellow structural biologists,  I am contemplating why some choose the 
HRV3C protease site over TEV for their fusion proteins.  Does anyone know?  Can 
HRV3C be made easily in homelab?  Does anyone have a plasmid?  Thank you, G

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