Dear Frank,

I may see in the attached pic several nucleation points and a considerable
amount of microcrystals. Based to my knowledge decreasing the concentration
of the precipitant and/or the protein concentration would be a reasonable
approach to refine the initial hits.
By checking the diagram as you correctly mentioned you may see that the
fine tuning of protein and precipitant concetration may lead to the
desirable result without reaching the precipitation zone.

Patrick just check your screens. Just a rule of thumb, if you see
precipitation in the ~60% of your drops then you should definitely reduce
the protein concentration.

ps dont forget to try the *streak seeding*, as well.

Have a nice day and again good luck.

Vicky

On Wed, Jul 12, 2017 at 8:50 AM, Frank von Delft <
frank.vonde...@sgc.ox.ac.uk> wrote:

> Actually, you should try *increasing* the protein concentration - a lot.
> But be prepared to drop the precipitant concentration to almost nothing (1
> or 2% isn't "low").
>
> To understand why, look at the phase diagram and what we assume about
> vapour diffusion.  (Which I'm assuming is what you're doing.)
>
>
> On 12/07/2017 06:28, Vicky Tsirkone wrote:
>
> Dear Patrick,
>
> You may reduce the protein concentation, as well.
> Another option could be the *streak seeding* by exploiting the drop of
> your initial condition.
>
> Good luck,
>
> V.T.
>
> On Mon, Jul 10, 2017 at 7:17 PM, Patrick Shaw Stewart <
> patr...@douglas.co.uk> wrote:
>
>>
>> Microseed them into two or three random screens.
>>
>> Search for MMS and rMMS online.
>>
>> Good luck
>>
>> Patrick
>>
>>
>>
>>
>> On 10 July 2017 at 15:47, Liuqing Chen <519198...@163.com> wrote:
>>
>>> hello everyone!
>>> I get a condition (10% w/v PEG 6000, 100mm HEPES PH7.0) in which my
>>> protein grow small  needle like crystals, how can i optimize it to get
>>> bigger crystals?  the attach is the crystals  figure.
>>> thanks in advance
>>> sincerely
>>> Liuqing Chen
>>>
>>
>>
>>
>> --
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>
>
>

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