TY - JOUR

T1 - A fine grained parallel smooth particle mesh Ewald algorithm for biophysical simulation studies

T2 - Application to the 6-D torus QCDOC supercomputer

AU - Fang, Bin

AU - Martyna, Glenn

AU - Deng, Yuefan

N1 - Funding Information:
This project is supported by the BNL LDRD grant #36930 entitled “Molecular dynamics on ultrascalable supercomputer” and IBM.

PY - 2007/8/15

Y1 - 2007/8/15

N2 - In order to model complex heterogeneous biophysical macrostructures with non-trivial charge distributions such as globular proteins in water, it is important to evaluate the long range forces present in these systems accurately and efficiently. The Smooth Particle Mesh Ewald summation technique (SPME) is commonly used to determine the long range part of electrostatic energy in large scale molecular simulations. While the SPME technique does not give rise to a performance bottleneck on a single processor, current implementations of SPME on massively parallel, supercomputers become problematic at large processor numbers, limiting the time and length scales that can be reached. Here, a synergistic investigation involving method improvement, parallel programming and novel architectures is employed to address this difficulty. A relatively simple modification of the SPME technique is described which gives rise to both improved accuracy and efficiency on both massively parallel and scalar computing platforms. Our fine grained parallel implementation of the modified SPME method for the novel QCDOC supercomputer with its 6D-torus architecture is then given. Numerical tests of algorithm performance on up to 1024 processors of the QCDOC machine at BNL are presented for two systems of interest, a β-hairpin solvated in explicit water, a system which consists of 1142 water molecules and a 20 residue protein for a total of 3579 atoms, and the HIV-1 protease solvated in explicit water, a system which consists of 9331 water molecules and a 198 residue protein for a total of 29508 atoms.

AB - In order to model complex heterogeneous biophysical macrostructures with non-trivial charge distributions such as globular proteins in water, it is important to evaluate the long range forces present in these systems accurately and efficiently. The Smooth Particle Mesh Ewald summation technique (SPME) is commonly used to determine the long range part of electrostatic energy in large scale molecular simulations. While the SPME technique does not give rise to a performance bottleneck on a single processor, current implementations of SPME on massively parallel, supercomputers become problematic at large processor numbers, limiting the time and length scales that can be reached. Here, a synergistic investigation involving method improvement, parallel programming and novel architectures is employed to address this difficulty. A relatively simple modification of the SPME technique is described which gives rise to both improved accuracy and efficiency on both massively parallel and scalar computing platforms. Our fine grained parallel implementation of the modified SPME method for the novel QCDOC supercomputer with its 6D-torus architecture is then given. Numerical tests of algorithm performance on up to 1024 processors of the QCDOC machine at BNL are presented for two systems of interest, a β-hairpin solvated in explicit water, a system which consists of 1142 water molecules and a 20 residue protein for a total of 3579 atoms, and the HIV-1 protease solvated in explicit water, a system which consists of 9331 water molecules and a 198 residue protein for a total of 29508 atoms.

KW - 3D-FFT

KW - Biomolecular simulations

KW - Particle Mesh Ewald

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U2 - 10.1016/j.cpc.2007.01.011

DO - 10.1016/j.cpc.2007.01.011

M3 - Article

AN - SCOPUS:34447343768

VL - 177

SP - 362

EP - 377

JO - Computer Physics Communications

JF - Computer Physics Communications

SN - 0010-4655

IS - 4

ER -