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Hi Nicola,

We have had success simply soaking zinc into the crystal prior to data collection. This has worked very well for a number of proteins. We simply add some zinc to the cryo-protectant and leave it to soak for various times.

Hope this helps.

Kind regards
Sheena







Sheena McGowan
Head, Structural Microbiology Laboratory
Monash Biomedicine Discovery Institute and Department of Microbiology
Adjunct Senior Research Fellow | Monash Institute of Pharmaceutical Sciences
Monash University 
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Lorne Conference for Protein Structure and Function <http://lorneproteins.org/>
10th - 14th February, 2019

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> On 10 Dec 2018, at 8:31 am, Nicola Evans <[log in to unmask]> wrote:
> 
> From a fluorescence scan it would appear a protein I am working on has zinc in it. The occupancy is likely to be very low however (a structural homologue has several zincs in the x-ray crystal data but at 0.5 occupancy), as there isn't anything obvious in the electron density map (perhaps some of the waters are zinc) and an anomalous difference map wasn't possible to obtain on our last beamtime. 
> 
> Ideally I would want to re-express the protein with zinc added to the culture conditions, but I am time-restained, so I was wondering if it is possible to add zinc to purified protein instead? I have heard it can cause proteins to crash out. I have quite a lot of protein frozen so I can try a few things. I would appreciate any advice on how much to add from anyone who has had success with this before? 
> 
> Thanks in advance!
> 
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