Charged binding calculations

Authored by Gabriel Rocklin, last updated July 1 2014 STILL IN PROGRESS

Overview

Many interesting processes involve ions changing chemical environment, such as the transfer of an ion from the gas phase to the solvated phase, the protonation of a protein side chain, or the binding of a charged ligand. Free energy simulations of these processes can be done in two ways: (1) the same simulated system can be used for both chemical environments, such as when a charged ligand is "pulled" from a protein binding site into the bulk solvent, or (2) different simulated systems can be used for different chemical environments, such as when a charged ligand is alchemically decoupled from its own "free in solution" box and alchemically inserted/coupled into the protein binding site in a different simulated system. In both cases, the computed free energies can depend on details of the calculation setup, such as the boundary conditions applied at the edge of the explicit solvent system (periodic, implicit solvent, or vacuum), the size of the periodic unit cell, and even completely arbitrary details of the solvent molecular topology.

These dependences on setup parameters are referred to as "finite size effects" because they are caused by the finite and extremely small size of the simulated system/periodic unit cell relative to the macroscopic size of the experimental system. Finite size effects are basically computational artifacts because they contribute to the simulated free energy change but not to a bulk experimental measurements. It is thus desirable to remove these free energy contributions before comparing simulated free energy results with experimental results.

The conventional way to do this is to introduce correction terms to convert the raw simulation results (which are specific to the particular choices of boundary condition, system size, molecular topology, etc) into corrected results based on ideal physical conditions, meaning that the solute is infinitely diluted in a nonperiodic bulk of solvent. Once simulation results have been corrected to match these ideal conditions, different simulation methods can be compared to each other without confounding artifacts, and simulation results can be compared with experimental results. (Of course, bulk experiments are not exactly performed under true ideal conditions either, but the non-idealities in experiments have little to do with finite size artifacts in simulations (periodic or otherwise) so it is still best to correct simulation results for these artifacts prior to comparisons with experimental results.)

This page provides short guidance on how to remove finite size artifacts for several common simulation approaches. For full details see the associated references. Note that the only types of artifacts considered here are those relating to the net charge of the investigated species (for instance, the charged ligand). For now, this page only covers simulations performed under periodic boundary conditions.

Periodic boundary conditions alter the electric field in the unit cell

The key difference between periodic boundary conditions and nonperiodic boundary conditions is how "zero" potential is defined. Under nonperiodic boundary conditions, zero is defined as the potential infinitely far from the system of interest.

[math]\displaystyle{ \Phi_{Nonper} (r=\infin) = 0 }[/math]

However, under periodic boundary conditions, zero potential is defined as the average potential over the periodic unit cell.

[math]\displaystyle{ \left \langle \Phi_{Per}(r) \right \rangle = 0 }[/math]

This requirement of average zero potential means that any perturbation to the average potential in the unit cell will alter the potential felt at every point in the unit cell even if no external electric field is produced. For example, a neutral sphere with a point negative charge at the center and a uniform shell of positive charge on the outside produces no electric field outside itself. However, there is a net negative potential inside the sphere. If this sphere is placed in a periodic unit cell, the overall negative potential inside the sphere produces a compensating uniform positive potential across the rest of the unit cell in order to maintain the zero average potential in the periodic unit cell.

Scenario 1: Alchemical annihilation of a charge in a periodic system

In an alchemical annihilation calculation, a charge is removed from a system over a series of simulated lambda intermediates. In most cases the charge is re-introduced in a different system, such as when a ligand is alchemically removed from bulk solvent and inserted into a protein binding site. In these calculations, the charge annihilation free energies depend on the electrostatic potential at the location of the charge, as calculated in the simulation model under periodic boundary boundary conditions. When a uniform potential is added to the box to maintain the required average potential of zero, the charge of interest feels this added artifactual potential. This is how the requirement that [math]\displaystyle{ \left \langle \Phi_{Per}(r) \right \rangle = 0 }[/math] alters binding free energies. To correct the simulated binding affinities, we need to understand the factors that alter [math]\displaystyle{ \left \langle \Phi_{Per}(r) \right \rangle }[/math].

Three main factors alter [math]\displaystyle{ \left \langle \Phi_{Per}(r) \right \rangle }[/math] and thus introduce finite size artifacts:

(1) Net charges in the system. All charges change the average potential in the unit cell. As a result, a "compensating background charge" is introduced which depends on the size of the periodic unit cell.

(2) The number density of water molecules in the system. Each water molecule behaves like the sphere in the above example - a negative charge on the inside and a positive charge on the outside. The magnitude of the compensating potential depends on the average potential inside the water molecule (which depends on which specific water topology is used), the number of water molecules in the box, and the size of the box.

(3) Complex charge distributions and excluded volume. If the simulation system contains a protein, the protein's charge distribution can change the average potential of the unit cell. The excluded volume of a large solute can also alter the average potential in the unit cell by changing the effective dielectric over some region of space from high (solvent like) to low (protein like).

A final type of finite size artifact does has nothing to do [math]\displaystyle{ \left \langle \Phi_{Per}(r) \right \rangle }[/math]. Unlike an infinite nonperiodic system, a periodic unit cell has only a limited amount of solvent. This means that an ion in a periodic system is "undersolvated" relative to the infinite dilution case. A correc

Scenario 2: Protein-ligand binding in the same box

A common approach for calculating protein-ligand binding is to compute the potential of mean force (PMF) of "pulling" the ligand out of the protein binding side using artificial restraining potentials. The ligand is considered "unbound" once it is "suitably far" from the protein as to be considered non-interacting.