A computational Grid framework for immunological applications.

Philos Trans A Math Phys Eng Sci

Institute of Structural and Molecular Biology, School of Crystallography, Birkbeck College, Malet Street, London WC1E 7HX, UK.

Published: July 2009

AI Article Synopsis

  • A computational Grid has been developed to connect various resources globally, helping users bypass administrative and technical hurdles.
  • This project is part of the European Union's ImmunoGrid initiative, which aims to simulate the immune system at multiple levels and utilizes a wide range of computational resources across the Atlantic.
  • The Grid has facilitated the processing of 40,000 polypeptide sequences from influenza strains, generating over 14 million predictions and enabling advanced research in T-cell epitope prediction methods.

Article Abstract

We have developed a computational Grid that enables us to exploit through a single interface a range of local, national and international resources. It insulates the user as far as possible from issues concerning administrative boundaries, passwords and different operating system features. This work has been undertaken as part of the European Union ImmunoGrid project whose aim is to develop simulations of the immune system at the molecular, cellular and organ levels. The ImmunoGrid consortium has members with computational resources on both sides of the Atlantic. By making extensive use of existing Grid middleware, our Grid has enabled us to exploit consortium and publicly available computers in a unified way, notwithstanding the diverse local software and administrative environments. We took 40 000 polypeptide sequences from 4000 avian and mammalian influenza strains and used a neural network for class I T-cell epitope prediction tools for 120 class I alleles and haplotypes to generate over 14 million high-quality protein-peptide binding predictions that we are mapping onto the three-dimensional structures of the proteins. By contrast, the Grid is also being used for developing new methods for class T-cell epitope predictions, where we have running batches of 120 molecular dynamics free-energy calculations.

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http://dx.doi.org/10.1098/rsta.2009.0046DOI Listing

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