If there are backbone NMR assignments available then, definately a pH titration 
using HSQCs would give site specific information.  These are easy experiments 
if someone can help you set them up.
The perturbations should map to the inter-domain interface.

If there are no assignments for the protein, spectral changes in response to pH 
would be harder to interpret.  You could try FRET by introducing two probes - 
one in each domain.

Roopa

________________________________________
From: CCP4 bulletin board [ccp...@jiscmail.ac.uk] On Behalf Of Jacob Keller 
[j-kell...@fsm.northwestern.edu]
Sent: Monday, December 06, 2010 12:15 PM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] pH dependent conformational change

Wouldn't a HSQC of 15N-labeled protein be a relatively easy yes/no experiment? 
Maybe it would not be incredibly definitive?

Jacob


On Mon, Dec 6, 2010 at 11:10 AM, Mischa Machius 
<mach...@med.unc.edu<mailto:mach...@med.unc.edu>> wrote:
Daniel,

You'll probably have to monitor pH changes through size changes of your 
protein, provided the structural changes will indeed cause size changes.

You said "easy", so that probably rules out Small-Angle X-Ray Scattering 
(SAXS), but that would be the highest-resolution method. You can try static and 
dynamic light scattering, analytical ultracentrifugation and fluorescence 
anisotropy. If you are really lucky, size exclusion chromatography might work 
too.

And then there are the "difficult" ways...

MM




On Dec 6, 2010, at 11:59 AM, Daniel Jin wrote:


Dear CCP4 colleagues,



We have a protein that is composed of two domains connected by a short peptide 
linker. We have some indirect evidence showing that the two domains may somehow 
move against each other when exposed to different pH. It is unlikely to have 
any obvious secondary structure change since each domain behaves like a rigid 
body. I am wondering whether there is any “easy” way, biochemically or 
biophysically, to monitor the conformational changes in solution. Many thanks.



As far as I know most of the pH sensing stories are linked to histidine 
residue. Can you point me to any references that show a different pH sensing 
mechanism (other than His)? Thanks.



Best,

Daniel



-----------------------------------------------------------------------
Mischa Machius, PhD
Director, Center for Structural Biology
Assoc. Professor, Dept. of Pharmacology
Member, Lineberger Comprehensive Cancer Center
University of North Carolina
4079 Genetic Medicine
CB#7365
120 Mason Farm Road
Chapel Hill, NC 27599-7365, U.S.A.
tel: +1-919-843-4485
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Jacob Pearson Keller
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