Hello Jacob,

The problem for native gel is that it is much more sensitive to a single charge difference than size differences. Also, the gel pattern may change greatly if you use a different buffer system. I had a case 2 years ago that my protein ran at 5 positions on a Laemmli(pH 8.8) native gel, but only one position on a pH 7 gel. This protein only has one clean peak corresponding to the monomer size on SEC when loaded at 1mg/mL, pH 6.8. So I believe what I was seeing on the pH 8.8 gel was either some small conformational inhomogeneities(causing charged side chains to be more exposed or buried) or some kind of aggregation caused by the rather basic pH in the gel system - or even deamination or decarboxylations... maybe.

As an inexpensive alternative to normal native gels, there is another technique you might want to try: the blue native gel. In the blue native gels, the protein's charge will mainly come from bound Commassie Blue G250 molecues, so the migrating pattern should only reflect the size of the protein particle. But the downside is that you may have to spend some time to figure out your own protocol for your particular protein, since some protein may precipitate or aggregate badly with Commassie Blue G250 (and even worse if you use R250, which has ethyl instead of methyl groups).

If you have access to a DLS machine, it might be a much better judge for the disagreement between your SEC and AUC results.

Zhijie


Quoting Jacob Keller <j-kell...@md.northwestern.edu>:

Dear Crystallographers,

I am having trouble interpreting the attached native gel (which is very
repeatable, under various conditions). Is it tenable that various
charge states or conformations could account for this behavior, or must
it be various oligomeric states? AUC results seem to show only
monomers, whereas SEC shows a series of peaks. Mass-spec shows no
post-translational mods. Anyone have any similar experiences, or
references?

Thanks,

Jacob

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Jacob Pearson Keller
Northwestern University
Medical Scientist Training Program
Dallos Laboratory
F. Searle 1-240
2240 Campus Drive
Evanston IL 60208
lab: 847.491.2438
cel: 773.608.9185
email: j-kell...@northwestern.edu
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