It would probably be safe if you run dialysis first. If you still think that 
may harm the expensive SEC column then running PD-10 column first would be 
advised.

Hope this helps.
Vaheh Oganesyan, Ph.D.
[cid:image001.png@01D80EB0.8E5CA9A0]
R&D | Biologics Engineering
One Medimmune Way, Gaithersburg, MD 20878
T:  301-398-5851
vaheh.oganes...@astrazeneca.com<mailto:oganesy...@medimmune.com>


From: CCP4 bulletin board <CCP4BB@JISCMAIL.AC.UK> On Behalf Of Maria Jose 
Sanchez Barrena
Sent: Friday, January 21, 2022 9:59 AM
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] Glutaraldehyde and gel filtration

Dear all:

Can I ask for some help-opinion on possible problems for a superdex200 column 
to separate a glutaraldehyde-crosslinked sample?

We are using 0.1% Glutaraldehyde to crosslink and protein complex and after 
incubation, we stop the reaction by adding 50mM Tris buffer. We have analyzed 
the sample on an SDS-PAGE gel and we do not observe aggregates, only the 
crosslinked complex and some uncrosslinked protein.

We would like to further analyze this sample on a gel filtration Superdex 200 
Increase 3.2/300 column and although I cannot see any incompatibility in the 
column specifications, I would like to have some advice on how you deal with 
this. Since the glutaraldehyde is quenched with Tris, I imagine that passing 
this sample through the column would not make any harm in future purifications 
or will have a bad effect on resin stability. Would I need to wash the column 
with something special? Do you have columns dedicated to 
glutaraldhyde-containing samples? I am a bit concerned on “contaminating” the 
column or losing resolution in the future.

Many thanks in advance and all best wishes for 2022,

María J. Sánchez-Barrena
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