Thank you everyone for the detailed explanations/suggestions and sharing
your successful experience. It is very helpful.

Earlier I had thought that maybe with  ΔTm, I could select the most
promising molecules. But now it is unlikely the case.
I should have also mentioned that the IC50 values for all the compounds are
between 1-5uM.

Thanks again,
Have a wonderful weekend,
Saif


On Thu, Feb 25, 2021 at 7:38 PM Maria Cristina Nonato <[email protected]>
wrote:

> *Dear Saif*
>
> *Hope you are doing well and safe!*
>
> 1) How much change in Tm (ΔTm) in a thermal shift assay is considered to
> be significant ?
>
> *As it has already been mentioned there is no specific cutoff  for deltaTm
> to be considered significant. DeltaTm depends on many factors, including
> the type of dye you use, protein structure and where your compound binds*.
>
>
> 2) A negative  ΔTm infers that the compound is making the protein
> unstable. In such a case, will the co-crystallization be difficult or just
> impossible or on the contrary it shouldn't matter much?
>
>
> *A negative detaTm means the compound is binding to a different
> conformational state of the protein, compared to the native one. I would
> not consider co-crystallization more difficult or impossible in the
> presence of those compounds, but I would definitely screen for different
> crystallization conditions.*
>
> *Good luck*
>
> *Cristy*
> *#womeninscience*
>
>
> Em qui., 25 de fev. de 2021 às 11:56, Saif Mohd <[email protected]>
> escreveu:
>
>> Hello everyone,
>>
>> 1) How much change in Tm (ΔTm) in a thermal shift assay is considered to
>> be significant ?
>>
>> 2) A negative  ΔTm infers that the compound is making the protein
>> unstable. In such a case, will the co-crystallization be difficult or just
>> impossible or on the contrary it shouldn't matter much?
>>
>>
>> Thanks and best regards,
>> Saif
>>
>>
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