Hi Artem,

 

I have stayed away from these types of reagents in order to avoid
detergents, and also because of anecdotal reports that these work less
well for large-scale preps. Are you saying you use them routinely for
preps of crystal-grade protein? Am I being too concerned about the
presence of detergents?

 

Thanks,

Michael

 

________________________________

From: CCP4 bulletin board [mailto:[email protected]] On Behalf Of
Artem Evdokimov
Sent: Thursday, March 15, 2012 7:04 PM
To: [email protected]
Subject: Re: [ccp4bb] protein stain, B-PER

 

Hi :-)

These subjects come up regularly! Basically, in brief we use a nearly
magical mix of bper and yper in 3 to 1 ratio, supplemented with salt,
bensonaze and lysozyme. In my fairly extensive experience this works for
about 85 to 90 % of cytoplasmic proteins with no issues for affnity
chromatography and (if no salt is added) for ion exchange primary
capture. For the remaining 10% we try every other method under the sun.
For gels - 15 minute biorad gels are very nice (have to have 300v power
supply) and stain/destain in our hands is abou 5-15 minutes with a
microwave. We destain in boiling water, with no other chemicals
involved. Any coomassie based stin works well enough for this. Some ppl
in our lab love the stain free gels but you have to remembr to count trp
residues as it relies on trp chemistry to work.
In short, this (and a number of other tricks) makes it possible to have
a three step purification done in one 8 hr work day.

Artem

On Mar 15, 2012 10:25 AM, "Thomas Edwards" <[email protected]>
wrote:

Dear BB,

Apologies for being mildly off topic.
Maybe.


 1.  We are trying to express (in E. coli) a protein which appears to be
quite sensitive to mechanical disruption. We have ordered some B-PER
(Pierce - "B-PER Bacterial Protein Extraction Reagents are designed to
extract soluble protein from bacterial cells without harsh chemicals or
mechanical procedures like sonication"), but would like to try a variety
of similar things if possible. Any advice from the community out there?
Anybody know what goes into B-PER or similar things (I know there's some
Dnase and lysosyme in there - but which detergents are compatible with
Ni, GST, how much do you need etc)??
 2.  Staining SDS gels. There are various concerns from lab members
about safety re methanol in stains, microwaving stains etc etc. "Instant
Blue" claims to have none of these problems.  Quote: "Protein gel
staining takes around 15 minutes without the need to wash, fix,
microwave or destain". But again, I'd like to try things to see if they
work for us (before spending cash - yes, I am spending averse...!).
Anybody any suggestions for quick, non-fix, non-methanol, non-microwave,
non-destain protein gel stains? Have tried home made colloidal coomassie
but our protocol still requires fixes and washes that made it not really
worth while.

Happy to collate thoughts on replies offline and post summary.

Many thanks
Ed

T.A.Edwards Ph.D.
Deputy Director Astbury Centre for Structural Molecular Biology
Lecturer in Biochemistry
Garstang 8.53d
University of Leeds, Leeds, LS2 9JT
Telephone: 0113 343 3031
http://www.bmb.leeds.ac.uk/staff/tae/
-- No one should approach the temple of science with the soul of a money
changer.  ~Thomas Browne

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