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Characterisation of the SCR-domain family of Complement Regulators ; Structure, function and Streptococcal pathogenesis.

Characterisation of the SCR-domain family of Complement Regulators ; Structure, function and Streptococcal pathogenesis.
补体调节因子 SCR 结构域家族的表征;
批准号:
nhmrc : 275550
负责人:
Prof David Gordon
金额:
$28.86万
依托单位:
依托单位国家:
澳大利亚
项目类别:
NHMRC Project Grants
财政年份:
2004
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2004-01-01 至 2006-12-31

项目摘要

项目成果

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中文摘要
翻译
血液中一种叫做“补体”的蛋白质在外来细胞或微生物存在时被激活,这通常会导致它们的破坏。重要的是,这种破坏性活动是针对外来组织而不是自身组织的。这是由另一个蛋白质家族实现的,包括一种叫做因子H的蛋白质,它可以关闭或调节补体活性。这些蛋白质是如何工作的是这个项目的主要焦点。有许多疾病的损害是由无意的补体激活引起的,调节蛋白在这一领域具有治疗潜力。此外,许多应该被补体消灭的细菌和其他微生物通过结合调节蛋白而逃脱。了解这是如何实现的,可能有助于确定疫苗开发的目标。
英文摘要
A group of proteins in blood called 'Complement' are activated in the presence of foreign cells or micro-organisms and this generally results in their destruction. It is important that this destructive activity is directed against foreign and not self tissue. This is achieved by a further family of proteins, including a protein called factor H, which switch off or regulate complement activity. How these proteins work is the principle focus of this project. There are many diseases in which damage results from inadvertent complement activation and the regulatory proteins have therapeutic potential in this area. In addition, many bacteria and other micro-organisms, which should be destroyed by complement, escape by binding regulatory proteins. Understanding how this is achieved may assist in identifying targets for vaccine development.
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会议论文
E. coli as an indicator of faecal contamination in the Australian context
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  • 资助金额:
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  • 财政年份:
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An apotope of Ro60 in lupus
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H1N1 Development of recombinant GPI-anchored haemagglutinin of swine influenza H1N1 for serological and immunological st
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The ecological dynamics of secreted bacteriocins and the evolution of multiple bacteriocin production in Escherichia coli
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  • 项目类别:
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  • 批准年份:
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