User:Nathan H. Kipniss/Notebook/20.109 Final Project
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[Media:S12_M2D7_TR-Orange.txt|Raw Titration Data] | [Media:S12_M2D7_TR-Orange.txt|Raw Titration Data] | ||
| - | + | [[Image:DSCN2024.JPG|thumb|left|400px|TR_BLUE_CELL_1_CORE_UP, T/R]] | |
| - | [Image:Plots,_fitted_Matlab.jpg] | + | [Image:Plots,_fitted_Matlab.jpg|thumb|center|Fitted Matlab binding curves] |
==Ideas== | ==Ideas== | ||
Revision as of 12:19, 1 May 2012
Elucidating the function of D24H Inverse Pericam mutant
Background
In module 2 of 20.109, we created the D24H mutant of inverse pericam. The experimental results from the calcium binding assay was surprising as calcium affinity decreased (Kd increase), yet cooperativtiy increased. For a final research idea, I would like to propose the set of experiments that would elucidate how the addition of a histidine into the first binding loop of inverse pericam can make these changes.
[Media:S12_M2D7_TR-Orange.txt|Raw Titration Data]
[Image:Plots,_fitted_Matlab.jpg|thumb|center|Fitted Matlab binding curves]
Ideas
-working under the assumption that the SDM did indeed work (sequencing with BLAST, discontinuous mega-blast suggests it did indeed work)
- consider looking at calmodulin only.
