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用于免疫应用的计算网格框架。

A computational Grid framework for immunological applications.

机构信息

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

出版信息

Philos Trans A Math Phys Eng Sci. 2009 Jul 13;367(1898):2705-16. doi: 10.1098/rsta.2009.0046.

DOI:10.1098/rsta.2009.0046
PMID:19487206
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.

摘要

我们开发了一个计算网格,通过单个接口利用一系列本地、国家和国际资源。它使用户尽可能远离与管理边界、密码和不同操作系统功能有关的问题。这项工作是作为欧盟免疫网格项目的一部分进行的,该项目的目标是开发分子、细胞和器官水平免疫系统的模拟。免疫网格联盟的成员在大西洋两岸都有计算资源。通过广泛利用现有的网格中间件,我们的网格使我们能够以统一的方式利用联盟和公开可用的计算机,尽管存在各种本地软件和管理环境。我们从 4000 种禽和哺乳动物流感株中获取了 40000 个多肽序列,并使用神经网络对 120 个 I 类 T 细胞表位预测工具进行了 I 类等位基因和单倍型的预测,生成了超过 1400 万个高质量的蛋白质-肽结合预测,我们正在将这些预测映射到蛋白质的三维结构上。相比之下,网格也被用于开发用于 I 类 T 细胞表位预测的新方法,我们在那里运行了 120 个分子动力学自由能计算的批处理。

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