I would try it both ways and see what you get.  Also do controls of buffer into 
each protein

For extra info could also try with SPR.  Always best to do these things using 
multiple complimentary methods

Best wishes

Clare

From: CCP4 bulletin board <CCP4BB@JISCMAIL.AC.UK> On Behalf Of Bernhard Rupp
Sent: 03 October 2019 16:06
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] ITC question -dimer vs monomer

Hi Fellows,

please let me ask the respective experts an ITC question: I have 2 proteins, 
stable and dialyzed in identical buffer.
A is a monomer and B an obligate dimer. I suspect that eventually a A2B2 dimer 
will form.

Intuitively, it should make a difference whether I titrate the dimer with the 
monomer or vice versa.
In the first case, a momomer would initially meet a lot of free dimers, and I 
would expect that randomly, a AB2 complex
is more likely to form than a A2B2 (let's disregard any more complex 
colligative/cooperative effects).

If I drip the dimer into the monomer pool, it is quite likely that the B dimer 
meets 2 free As, and I get right away a higher population of A2B2s.

Maybe at dilutions of ITC and with sufficient equilibration that is not an 
issue at all (again, absent any cooperative effects that might alter the first 
Kd vs. the second, despite the sites on the dimer are at least initially 
equivalent).

Can someone guide me towards literature about this or perhaps share some 
first-hand experience?

Many thanks, BR

------------------------------------------------------
Bernhard Rupp
http://www.hofkristallamt.org/
b...@hofkristallamt.org<mailto:b...@hofkristallamt.org>
+1 925 209 7429
+43 676 571 0536
------------------------------------------------------
Many plausible ideas vanish
at the presence of thought
------------------------------------------------------


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