CHARMM

CHARMM
Developer(s) Martin Karplus, Accelrys
Initial release 1983 (1983)
Stable release c39b1 / 15 August 2014 (2014-08-15)
Preview release c40a1 / 15 August 2014 (2014-08-15)
Written in FORTRAN 77/95
Operating system Unix-like
Type molecular dynamics
License Proprietary
Website charmm.org

CHARMM (Chemistry at Harvard Macromolecular Mechanics) is the name of a widely used set of force fields for molecular dynamics as well as the name for the molecular dynamics simulation and analysis package associated with them.[1][2][3] The CHARMM Development Project involves a network of developers throughout the world working with Martin Karplus and his group at Harvard to develop and maintain the CHARMM program. Licenses for this software are available, for a fee, to people and groups working in academia.

CHARMM force fields

The CHARMM force fields for proteins include: united-atom (sometimes called "extended atom") CHARMM19,[4] all-atom CHARMM22[5] and its dihedral potential corrected variant CHARMM22/CMAP.[6] In the CHARMM22 protein force field, the atomic partial charges were derived from quantum chemical calculations of the interactions between model compounds and water. Furthermore, CHARMM22 is parametrized for the TIP3P explicit water model. Nevertheless, it is frequently used with implicit solvents. In 2006, a special version of CHARMM22/CMAP was reparametrized for consistent use with implicit solvent GBSW.[7]

For DNA, RNA, and lipids, CHARMM27[8] is used. Some force fields may be combined, for example CHARMM22 and CHARMM27 for the simulation of protein-DNA binding. Additionally, parameters for NAD+, sugars, fluorinated compounds, etc. may be downloaded. These force field version numbers refer to the CHARMM version where they first appeared, but may of course be used with subsequent versions of the CHARMM executable program. Likewise, these force fields may be used within other molecular dynamics programs that support them.

In 2009, a general force field for drug-like molecules (CGenFF) was introduced. It "covers a wide range of chemical groups present in biomolecules and drug-like molecules, including a large number of heterocyclic scaffolds".[9] The general force field is designed to cover any combination of chemical groups. This inevitably comes with a decrease in accuracy for representing any particular subclass of molecules. Users are repeatedly warned in Mackerell's website not to use the CGenFF parameters for molecules for which specialized force fields already exist (as mentioned above for proteins, nucleic acids, etc.).

CHARMM also includes polarizable force fields using two approaches. One is based on the fluctuating charge (FQ) model, also known as Charge Equilibration (CHEQ).[10][11] The other is based on the Drude shell or dispersion oscillator model.[12][13]

Parameters for all of these force fields may be downloaded from the Mackerell website for free.

CHARMM molecular dynamics program

The CHARMM program allows generation and analysis of a wide range of molecular simulations. The most basic kinds of simulation are minimization of a given structure and production runs of a molecular dynamics trajectory.

More advanced features include free energy perturbation (FEP), quasi-harmonic entropy estimation, correlation analysis and combined quantum, and molecular mechanics (QM/MM) methods.

CHARMM is one of the oldest programs for molecular dynamics. It has accumulated a large number of features, some of which are duplicated under several keywords with slight variations. This is an inevitable result of the large number of outlooks and groups working on CHARMM throughout the world. The changelog file as well as CHARMM's source code are good places to look for the names and affiliations of the main developers. The involvement and coordination by Charles L. Brooks III's group at the University of Michigan is salient.

History of the program

Around 1969, there was considerable interest in developing potential energy functions for small molecules. CHARMM originated at Martin Karplus's group at Harvard. Karplus and his then graduate student Bruce Gelin decided the time was ripe to develop a program that would make it possible to take a given amino acid sequence and a set of coordinates (e.g., from the X-ray structure) and to use this information to calculate the energy of the system as a function of the atomic positions. Karplus has acknowledged the importance of major inputs in the development of the (at the time nameless) program, including

In the 1980s, finally a paper appeared and CHARMM made its public début. Gelin's program had by then been considerably restructured. For the publication, Bob Bruccoleri came up with the name HARMM (HARvard Macromolecular Mechanics), but it didn't seem appropriate. So they added a C for Chemistry. Karplus said: "I sometimes wonder if Bruccoleri's original suggestion would have served as a useful warning to inexperienced scientists working with the program."[14] CHARMM has continued to grow and the latest release of the executable program was made in August 2009 as CHARMM35b3.

Running CHARMM Under Unix/Linux

The general syntax for using the program is:

charmm -i filename.inp -o filename.out
charmm 
The actual name of the program (or script which runs the program) on the computer system being used.
filename.inp 
A text file which contains the CHARMM commands. It starts by loading the molecular topologies (top) and force field (par). Then one loads the molecular structures' Cartesian coordinates (e.g. from PDB files). One can then modify the molecules (adding hydrogens, changing secondary structure). The calculation section can include energy minimization, dynamics production, and analysis tools such as motion and energy correlations.
filename.out 
The log file for the CHARMM run, containing echoed commands, and various amounts of command output. The output print level may be increased or decreased in general, and procedures such as minimization and dynamics have printout frequency specifications. The values for temperature, energy pressure, etc. are output at that frequency.

CHARMM and Volunteer Computing

Docking@Home, hosted by University of Delaware, one of the projects which use an open source platform for the distributed computing, BOINC, used CHARMM to analyze the atomic details of protein-ligand interactions in terms of Molecular Dynamics (MD) simulations and minimizations.

World Community Grid, sponsored by IBM, ran a project called The Clean Energy Project which also used CHARMM in its first phase which has completed.

See also

References

  1. ↑ Brooks BR, Bruccoleri RE, Olafson BD, States DJ, Swaminathan S, Karplus M (1983). "CHARMM: A program for macromolecular energy, minimization, and dynamics calculations". J Comp Chem 4 (2): 187–217. doi:10.1002/jcc.540040211.
  2. ↑ MacKerell, A.D., Jr.; Brooks, B.; Brooks, C. L., III; Nilsson, L.; Roux, B.; Won, Y.; Karplus, M. (1998). "CHARMM: The Energy Function and Its Parameterization with an Overview of the Program". In Schleyer, P.v.R.; et al. The Encyclopedia of Computational Chemistry 1. Chichester: John Wiley & Sons. pp. 271–277.
  3. ↑ Brooks BR, Brooks CL 3rd, Mackerell AD Jr, Nilsson L, Petrella RJ, Roux B, Won Y, Archontis G, Bartels C, Boresch S, Caflisch A, Caves L, Cui Q, Dinner AR, Feig M, Fischer S, Gao J, Hodoscek M, Im W, Kuczera K, Lazaridis T, Ma J, Ovchinnikov V, Paci E, Pastor RW, Post CB, Pu JZ, Schaefer M, Tidor B, Venable RM, Woodcock HL, Wu X, Yang W, York DM, Karplus M (29 July 2009). "CHARMM: The biomolecular simulation program". Journal of Computational Chemistry 30 (10): 1545–1614. doi:10.1002/jcc.21287. PMC 2810661. PMID 19444816.
  4. ↑ Reiher, III WH (1985). "Theoretical studies of hydrogen bonding". PhD Thesis at Harvard University.
  5. ↑ MacKerell, Jr. AD; et al. (1998). "All-atom empirical potential for molecular modeling and dynamics studies of proteins". J Phys Chem B 102 (18): 3586–3616. doi:10.1021/jp973084f.
  6. ↑ MacKerell, Jr. AD, Feig M, Brooks, III CL (2004). "Extending the treatment of backbone energetics in protein force fields: limitations of gas-phase quantum mechanics in reproducing protein conformational distributions in molecular dynamics simulations". J Comput Chem 25 (11): 1400–1415. doi:10.1002/jcc.20065. PMID 15185334.
  7. ↑ Brooks CL, Chen J, Im W (2006). "Balancing solvation and intramolecular interactions: toward a consistent generalized born force field (CMAP opt. for GBSW)". J Am Chem Soc 128 (11): 3728–3736. doi:10.1021/ja057216r. PMC 2596729. PMID 16536547.
  8. ↑ MacKerell, Jr. AD, Banavali N, Foloppe N (2001). "Development and current status of the CHARMM force field for nucleic acids". Biopolymers 56 (4): 257–265. doi:10.1002/1097-0282(2000)56:4<257::AID-BIP10029>3.0.CO;2-W. PMID 11754339.
  9. ↑ Vanommeslaeghe K, Hatcher E, Acharya C, Kundu S, Zhong S, Shim J, Darian E, Guvench O, Lopes P, Vorobyov I, Mackerell AD Jr (2009). "CHARMM general force field: A force field for drug-like molecules compatible with the CHARMM all-atom additive biological force fields". J Comput Chem 31 (4): 671–90. doi:10.1002/jcc.21367. PMC 2888302. PMID 19575467.
  10. ↑ Patel S, Brooks CL 3rd (2004). "CHARMM fluctuating charge force field for proteins: I parameterization and application to bulk organic liquid simulations". J Comput Chem 25 (1): 1–15. doi:10.1002/jcc.10355. PMID 14634989.
  11. ↑ Patel S, Mackerell AD Jr, Brooks CL 3rd (2004). "CHARMM fluctuating charge force field for proteins: II protein/solvent properties from molecular dynamics simulations using a nonadditive electrostatic model". J Comput Chem 25 (12): 1504–1514. doi:10.1002/jcc.20077. PMID 15224394.
  12. ↑ Lamoureux G, Roux B (2003). "Modeling induced polarization with classical Drude oscillators: Theory and molecular dynamics simulation algorithm". J Chem Phys 119 (6): 3025–3039. Bibcode:2003JChPh.119.3025L. doi:10.1063/1.1589749.
  13. ↑ Lamoureux G, Harder E, Vorobyov IV, Roux B, MacKerell AD (2006). "A polarizable model of water for molecular dynamics simulations of biomolecules". Chem Phys Lett 418: 245–249. Bibcode:2006CPL...418..245L. doi:10.1016/j.cplett.2005.10.135.
  14. ↑ Karplus M (2006). "Spinach on the ceiling: a theoretical chemist's return to biology". Annu Rev Biophys Biomol Struct 35 (1): 1–47. doi:10.1146/annurev.biophys.33.110502.133350. PMID 16689626.

External links

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