Team:EPF-Lausanne/Results/ELS

From 2009.igem.org

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Light state simulation




We run a a 62ns simulation on the 2v0w light state using 32 processors. Here is a video.

Validation of the light state simulation

PVT

Here are the values of pressure, volume and temperature for this run.

2v0w sim PVT.jpg

RMSD

The RMSD along the run gives:

2v0w sim rmsd.jpg


The RMSD is another test for the analysis of the evolution of the global structure of a protein. It computes the mean quadratic distance between the structure throughout the simulation, and the original crystallographic structure. It takes into account the scalar distance between atoms comparing two structures, after that these structures had been superposed.

RMSF

This analysis is in the continuity of the RMSD analysis: RMSF takes the average over time, giving a value for each particle i, while with RMSD, the average is taken over the particles, giving time specific values. And the RMSF plot gives us :

2v0w sim rmsf.jpg



Analysis of the simulation

As for the dark state, we tried to find a change in the j-alpha helix then looked at the comportment of the residues.

Angle between beta sheet and alpha helix

We ploted the angle between the helix and a strand of the beta sheet. As in the light state we don't see a clear movement.

2v0w sim angoli.jpg

GLN513 - ASN414

We also redid the same experiments as in the dark state. Here is the plot of the dihedral angle of GLN513 and ASN414. In this case, both residues don't switch to another conformational state.

2v0w dihed 513 414.jpg

CYS450 - FMN

Same study than in the dark state for the residue n° 450 was made here, with an important difference to point out which is the covalent bond between the residue 450 and the cofactor.

Here is the covalent bond between the cystein 450 and the cofactor, FMN:

Light conf cov.jpg


Here we plot the dihedral angle of this residue to see how it moves along time. As expected, the residue is now stable because of the covalent bond to the FMN.

Dih Light WT.png