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CCP4BB  January 2010

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Subject:

Re: Expression of large proteins in E. coli

From:

Raji Edayathumangalam <[log in to unmask]>

Reply-To:

Raji Edayathumangalam <[log in to unmask]>

Date:

Wed, 13 Jan 2010 17:22:39 -0500

Content-Type:

text/plain

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Hey Nick,

Short answer is that there are no magical tricks, as you probably  
already expect to hear. Seems there's a lot that you are trying already.

I have some limited experience with some 125kDa, 100kDa proteins.

1. I've had some luck with the E. coli C41, C43 strains. Especially if  
your proteins are inherently toxic to E. coli. There are commercial  
vendors who sell these strains with the plus or minus pLysS options.
2. Try moving the tags to the other terminus N- to C- or vice versa.  
Can't do that for SUMO in any easy manner.
3. Try MBP tag as well
4. Try Studier's autoinduction protocol
5. Try expression with chaperone kit,  trigger factor (Takara)
6. You don't mention whether the protein is human etc., but you may  
have to move to yeast or insect cells, in the worst case.

DISCLAIMER: I am not paid by Takara to mention their kit.

Good luck!
Raji

-----------
Raji Edayathumangalam
Joint Research Fellow
Brigham and Women's Hospital/
Harvard Medical School
Brandeis University




On Jan 13, 2010, at 4:53 PM, [log in to unmask] wrote:

> Hello All,
>
> I apologize for the non-CCP4-related query. I have been working for  
> several weeks now trying, with limited success, to express some very  
> large proteins (ranging from ~100 to 180 kDa) from pET15b in E.  
> coli. "Limited success" means I have expressed enough soluble  
> protein to see on a gel, but not enough to purify. I have tried the  
> obvious tweaks - changing strains (BL21, BL21-star, Rosetta, pLysS),  
> screening induction temperature (16 to 37C), [IPTG] (0.3-1.0mM). I  
> am in the process of subcloning into vectors for (1) SUMO fusion and  
> (2) periplasmic expression (pET26b). I get the sense from digging  
> through the literature that high level expression of large proteins  
> depends mostly on the individual protein and I will ultimately have  
> to look for homologs. But, this is my first experience expressing  
> such large proteins and I am curious to know if anyone out there has  
> some magical trick they wouldn't mind sharing.
>
> Thanks in advance,
> Nick
>
> -----------------------------------------
> Nicholas R. Silvaggi, Ph.D.
> University of Wisconsin-Milwaukee
> Department of Chemistry and Biochemistry
> 3210 North Cramer Street
> Milwaukee, WI 53211
>
> Phone: 414-229-2647
> Email: [log in to unmask]

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