Hi, 

 

We got some good experiences using the IBA streptag for baculo-expressed 
proteins. You'll have to redo the cloning, but it will be worth your while when 
you see the first purification step,

 

cheers

Joost

 

-----Original Message-----
From: CCP4 bulletin board [mailto:[EMAIL PROTECTED] On Behalf Of Alex Berndt
Sent: Wednesday, 28 February, 2007 20:21
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] Cannot running NTA to purify the protein having His-tag?

 

sometimes the insect cell medium intereferes (for whatever reasons) with nta 
purifications when they ar employed as a first step in the purification scheme. 
i experienced that occasionally. this can easily be circumvented by doing an 
ion exchange step beforehand! 

alternatively you might want to introduce a linker between your protein and the 
his-tag or create a 8xhis or 10xhis tag to enhance bing to the nta matrix. make 
sure you wash your cells from residual medium before you freeze your pellets.

 

alex

 

On 28 Feb 2007, at 19:18, Juergen Bosch wrote:





Ngo Duc Tri wrote:

 

        Dear CCP4 users,

         

        I'm purifying a kind of protease having His-tag. The protein is 
expressed in insect cells and broken by sonication.

        I used NTA resin to purify this protein.

        Buffer A is 50mM phosphate buffer pH 7.5 and 300mM NaCl. Buffer B is 
50mM phosphate buffer pH 7.5, 300 mM NaCl and 300 mM Imidazole.

        However, all proteins cannot bind to NTA resin. My protein is eluted in 
Flow-through. I also check the NTA resin with the control His-tag. The western 
blot also shows that my protein has His-tag.

         

        Do you have any ideas about my problem? I'm really appreciate all of 
your advices how to solve this. Thank you very much!

         

        My best regards,

        TriNgo

        Sungkyunkwan University

         

You His tag is most likely inaccessible, can you easily change the tag from e.g 
the N-terminus to the C-terminus ? Or if you have a structural homolog you 
could add the His tag into a loop, which is exposed.

 

Alternatively you can purify your protein under denaturing conditions using 8 M 
urea and refold it if you dare :-)

 

Juergen

 

-- 

Jürgen Bosch

University of Washington

Dept. of Biochemistry, K-426

1705 NE Pacific Street

Seattle, WA 98195

Box 357742

Phone:  +1-206-616-4510

FAX:    +1-206-685-7002

 

---

Alex Berndt

MRC Laboratory of Molecular Biology

Hills Road

Cambridge CB2 2QH

UK

 

mail     : [EMAIL PROTECTED]

phone : +44 (0)1223 402113

---

 





 


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