Modeling

To do

- Model allosteric interactions between LOVTAP & TrpR

What will be done:

- Model of LOVTAP in dark phase

- Model of LOVTAP in light phase

- Characterize how the J-alpha helix changes

- Model sturctural changes that enhance the switch feature of LOVTAP e.g. in dark phase: really weak interaction between LOVTAP and the corresponding DNA sequence, in light phase: strong binding of LOVTAP on DNA.

Modeling reference

LOVTAP simulation

We will follow the following article protocol:
Freddolino, P.L., Dittrich M., Schulten K., Dynamic Switching Mechanisms in LOV1 and LOV2 Domains of Plant Phototropins. Biophysical Journal, 91, 3630-3639, 2006 (Pubmed)

VMD informations

VMD is used to visualize molecules. It is quite user friendly.

• A tutorial for VMD can be found here.

NAMD informations

NAMD performs minimization and equilibration.

• A tutorial is on the same page as for VMD, here.
• NAMD 2.7b1 User's Guide

Run a simulation

A simulation is composed of different steps. Here are a few links that deal with heating and stabilization.

• Building Gramicidin A: Equilibration: protocol uses a single .conf file, heating process is too fast.
• NAMD notes from Robinson Lab: a really nice heating process, but involves different .conf files, which is really painful.

Implementation of the simulation

LOV domains are the light-sensitive portion of phototropins. They absorb light through a flavin cofactor, photo-chemicaly form a covalent bond between the chromophore and a cysteine residue in the protein, and proceed to mediate activation of an attached kinase domain.

Generating input files

First we need a compatible .pdb in addition to parameter and topology files. Steps to generate all the input files are explained in detail on this page How to generate input files. This is a kind of summary of the tuto.

.conf parameters

We should explain here what are the keywords we use in the .conf.

Run a complete simulation

We start from .pdb, .psf, .rtf generated in the previous section. Complete process is on a separate page How to run a simulation.

Molecular dynamics theory

Molecular dynamics simulation consists of the numerical, step-by-step, solution of the classical equations of motion. For this purpose we need to be able to calculate the forces acting on the atoms, and these are usually derived from a potential energy. This potential energy can be divided into:

• the non-bonded interactions:
  • The Lennard-Jones potential is the most commonly used form, with two parameters: σ, the diameter, and ε, the well depth. It takes into account the Van der Waals forces. It represents the non-bonded forces and the total potential energy can be calculated from the sum of energy contributions between pairs of atoms.

Lennard Jones potential

• • when electric charges are present, we add the Coulomb force

• the bonded interactions:

The protein moves thanks to different forces, which can be separated in bonded forces and non-bonded forces. The bonded forces correspond to

• the Lennard-Jones potential,

Coulomb force

To envisage

- Molecular mutationnal assay

Already done

Here is our first movie from the modeling, showing the behavior of the protein in the dark state condition: Dark State

After having modified some parameters in the parameter files, here is our second movie, concerning the light state of the protein this time, with the FMN: Light State with FMN without water