[RASMB] Holgers Mem-Prot. question
Ewa Folta-Stogniew
stogniew at yahoo.com
Tue Feb 17 17:32:00 PST 2004
How about running SEC with LS/RI/UV detection using
computed ext. coeff. It does work nicely (not always-
depends how well is the sample equilibrated) and the
apparent dn/dc (and amount of detergent present on the
peptide chain) can be determined from RI and UV
traces.
Please see slides 38-48 at:
http://info.med.yale.edu/wmkeck/biophysics/Final_10_25_02a_Wyatt.pdf
Also in published form at:
http://info.med.yale.edu/wmkeck/biophysics/reprints/Yernool_et_al_2003.pdf
Ewa
--- Lustig <ariel.lustig at unibas.ch> wrote:
>
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>
> Dear Holger and colleagues ,
> I join Jo's opinion that the determination of the
> concentration of a
> mem-prot MP
> in detergent solution is quasi impossible with
> conventional methods.
> Lets return to the roots!
> It took me years to learn that it is impossible to
> determine with
> pycnometrical
> methods (density-meter) detergents micelles or
> MP-complexes , first of
> all because
> the lack of the concentration knowledge. In such a
> solution we have 3
> sorts of
> particles 1 . under Cmc detergent, 2. over CMc
> detergent micelles(empty),
> 3. and
> MP-complexes.
> With SV and schlieren or interference optic =dn/dc
> you are able to see with
> OG or DM two sedimenting peaks the
> "empty"=detergent micelles -only and
> the MP-complexes, that one can indicate also by
> absorption optics. S' is
> also pressure dependent.
> Important in this case is
> that the detergent micelles have a density over 1
> (not like Octyl Poe,
> ro = about 1)
> The under Cmc can not be measured in this system.
> As I learned recently , the ratio of bound
> micelles is labile=unstable.
> I have submitted to BBA a short paper and will
> speak about this next
> in the
> Oxford-meeting.
> I do not prepare myself MP solutions but measure
> them and am happy if
> the OD
> fits to the cell thickness .
> Meanwhile no answer for you ariel
>
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