Hi Fred,
I am not sure if this has been brought up already. Another possibility might
be to generously pipet your Ni- or Co-matrix of choice directly to buffered
solubilized inclusion bodies, incubate for some time (even overnight if you
feel its necessary), and then use the slurry to pack a column for further
chromatographic manipulations. To quickly check if this approach might be
promising, you can do this on a small scale in epps.  IN fact working on a
small scale like this might allow you to test a number of buffer choices and
incubation protocols. You can spin down your beads followed by several
washing steps with your column buffer. You can then go two ways: (1) either
pellet with a hard spin and just add your SDS-PAGE sample buffer to the
pellet to visualize binding on gel (make sure you boil your sample) OR (2)
'elute' your protein with your imidazole-containing buffer followed by
analysis of the supernatant via SDS-PAGE. We have found that this approach
works quite well for difficult metal-affinity chromatography cases. 


Best wishes
Savvas




-----Original Message-----
From: CCP4 bulletin board [mailto:ccp...@jiscmail.ac.uk] On Behalf Of Fred
Sent: Wednesday, January 28, 2009 9:08 PM
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] [OFF TOPIC] his-tag doesn't bind

Just to let you know. No way, Talon also don't work. I am gonna try the 
GE His-trap column.

Fred wrote:
 > Hi everyone,
 > Thanks for answer my question. Just to add some more notes regarding 
to my expression system. The insert-vector (pET28) has been sequenced 
and the his-tag is N-terminal. The anti his-tag WB is positive and the 
binding buffer's pH is 8.2 (double-checked).
 > I had already experienced the same problem before, which I solved 
just increasing urea from 6M to 8M. Now, I have reached GndHCl 6M and no 
binding at all.
 > I'm currently running a SDS-PAGE with samples eluted from Talon and 
let you know the results.
 > All the Best,
 > Fred
 >>
 >>
 >> --- Fred /<ccp4bb.l...@gmail.com>/ schrieb am *Di, 27.1.2009:
 >> *
 >>
 >>     *Von: Fred <ccp4bb.l...@gmail.com>
 >>     Betreff: [ccp4bb] [OFF TOPIC] his-tag doesn't bind
 >>     An: CCP4BB@JISCMAIL.AC.UK
 >>     Datum: Dienstag, 27. Januar 2009, 22:00
 >>
 >>     *
 >>
 >>     *Hi ccp4 list,
 >>     I am trying to purify a his-tag protein by metal affinity 
chromatography. The
 >>     protein was expressed in inclusion bodies and its his-tag 
doesn't bind the
 >>     Qiagen Ni resin in denatured conditions (urea 8M or GndHCl 6M). 
Playing with
 >>     NaCl and detergents didn't help much.
 >>     Any help is appreciated.
 >>     Fred   *
 >>
 >>





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