Hi Chris,
Though there is no alternative to have a co-crystal structure it does not 
always happened to be the ideal case where you would easily get it 
co-crystallized in the same condition.
Soaking worked well in many cases, though definitely the answer is very 
dependent on a particular case to case basis as we all know. But as it seems 
the situation, that you have the native one crystallized, it is very quick 
process to check whether it is working for your system or not. If it would work 
that would make the rest of the story much easier and quicker.


Regarding the procedure details, you could add high concentration of ligand 
directly to the crystal drop but try to add the ligand carefully so that it 
take some time to get in contact with the protein crystals. If your ligand is 
water soluble that is the best scenario, if it is not and it is in DMSO try to 
dilute the DMSO concentration as much as possible. Just make a very high 
concentrated solution of your ligand with DMSO and then dilute it with water or 
buffer.

HTH

Thanks & Regards,
Saugata

Saugata Hazra
Postdoctoral Research Associate
Blanchard Lab
Albert Einstein Medical College
NY, USA



 
  


      

  


________________________________
 From: Christopher Browning <[email protected]>
To: [email protected] 
Sent: Thursday, September 12, 2013 6:25 AM
Subject: Re: [ccp4bb] Adding ligand to crystallization drop
 


Hi Again,

Thanks for the suggestions. I just tried it at 2 ligand concentrations and the 
crystals seem not to mind. The drop does go a little cloudy but I can't say if 
this is protein precipitation, or the ligand coming out of solution. My feeling 
its a bit of protein because of the high DMSO conc. being added. I'll 
co-crystallize just to have a backup!

Cheers

C 



-- 
Christopher Browning, Ph. D

Vertex Pharmaceuticals (Europe) Ltd
86-88 Jubilee Avenue
Milton Park
Abingdon
Oxfordshire
OX14 4RW
United Kingdom
 
Tel +44 (0) 1235 438327
[email protected]
www.vrtx.com
From: <Noinaj>, "Nicholas [E] (NIH/NIDDK)" <[email protected]>
Date: Thursday, 12 September 2013 10:21
To: Christopher Browning <[email protected]>, 
"[email protected]" <[email protected]>
Subject: RE: Adding ligand to crystallization drop


 
Chris,
 
Bottom line is that it is all dependent on how your ligand interacts with your 
protein, if there are any conformational changes, and how your crystals behave 
in such a dilution and high concentration of ligand.  You just have to test it 
and see, no way to know for sure until you do the experiments and see.  
However, there are some things to look for along the way.  For example, do your 
crystals crack after introducing the ligand or do they start to dissolve and 
lose their nice edges, or turn opaque?  you will probably also want to do a 
buffer only control without ligand to ensure that the crystals are ok with the 
dilution and change of environment.  
 
I assume the native crystals diffract well enough to solve the structure.  You 
would want to test crystals before any soaking and then with buffer only and 
then with ligand, to ensure diffraction is retained to a level useful enough 
for structure determination.  I did quite a bit of crystal soaking in grad 
school and it is something you just have to try since every crystal/protein is 
different. my experience is that soaking can often lead to a slight loss of 
resolution but typically you still get the information you are seeking if the 
crystals survive.
 
with that being said, soaking can sometimes lead to partial occupancy of your 
ligand.  So if you are able to do co-xtallization, i think that would be 
preferred and doesn't seem like too much additional effort assuming you are 
getting crystals in the same conditions as with native protein only.  and with 
co-xtallization, I often see slightly better resolution that with native 
protein only (not always the same condition though unfortunately).  But again, 
no way to know how your particular protein/crystal will behave without doing 
some pilot experiments first.  
 
Good luck!
 
 
 
 
 
Cheers,
Nick
 
 
 
--------------------------------
 
[ Nicholas Noinaj ]
the Buchanan Lab
Laboratory of Molecular Biology
LMB-NIDDK, NIH
50 South Drive, Room 4505
Bethesda, MD  20892-8030
1-301-594-9230 (lab)
1-859-893-4789 (cell)
[email protected]
 
[ the Buchanan Lab ]
http://www-mslmb.niddk.nih.gov/buchanan/
 
 
 
 
 
 
 
 
 
 
 
 
 
From:Christopher Browning [mailto:[email protected]] 
Sent: Thursday, September 12, 2013 4:37 AM
To: [email protected]
Subject: [ccp4bb] Adding ligand to crystallization drop
 
Hi,
 
I've just got a quick question about getting ligands bound to proteins in 
crystals. I've managed to co-crystallize my proteins with the various ligands, 
and I'm aware that soaking will work as well but I want to speed up the process.
 
Would this work? If I had a bunch of crystals that have grown in their drop, 
can I pipette the ligand (say 0.6ul to get a desired conc.) onto the drop and 
just let the crystals soak that way. Any dilution that would have occurred when 
then readjust as the drop will be sealed again. Perhaps the crystals would get 
a little stressed when adding the high concentrated ligand and this method 
would not work…?
 
Thanks,
 
Chris
 
 
 
-- 
Christopher Browning, Ph. D
 
Vertex Pharmaceuticals (Europe) Ltd
86-88 Jubilee Avenue
Milton Park
Abingdon
Oxfordshire
OX14 4RW
United Kingdom
 
Tel +44 (0) 1235 438327
[email protected]
www.vrtx.com
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