Hi Zhen,
I'm not sure that binding to a monoclonal antibody is good evidence that the protein is in a natively folded state. I would be suspicious of such a result as the protein could be improperly, which is causing it to interact with the column matrix. It could be useful to use some other techniques (Activity Assay, Circular Dichroism, DSC, Native Page etc. to validate the refolding).
Best,
Rhys
________________________________________
From: CCP4 bulletin board [[log in to unmask]] On Behalf Of Patrick Loll [[log in to unmask]]
Sent: 20 June 2013 20:39
To: [log in to unmask]
Subject: Re: [ccp4bb] Puzzling observation about size exclusion chromatography
If your protein elutes very late, that means it's binding to the column matrix (so all estimates of size go into the trash). Check to see that the ionic strength of buffer is reasonable (equivalent to, say, 150 mM NaCl). If so, then the only solution is to go to a different matrix type.
Pat
On 20 Jun 2013, at 3:09 PM, Zhang, Zhen wrote:
> Dear all,
>
> I just observed a puzzling phenomenon when purifying a refolded protein with size exclusion chromatography. The protein was solubilized by 8M Urea and refolded by dialysis against 500mM Arginine in PBS. The protein is 40KDal and is expected to be a trimer. The puzzling part is the protein after refolding always eluted at 18ml from the superdex S200 column (10/300), which is calculated to be 5KDal by standard. However, the fractions appear to be at 40KDal with SDS PAGE and the protein is functional in term of in vitro binding to the protein-specific monoclonal antibody. I could not explain the observation and I am wondering if anyone has the similar experience or has an opinion on this. Any comments are welcome.
>
> Thanks.
>
> Zhen
>
>
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