首页> 外国专利> FRAGMENTS OF THE PA SUBUNIT OF RNA DEPENDENT RNA POLYMERASE FROM PANDEMIC INFLUENZA VIRUS A 2009 H1N1, AND THEIR USE

FRAGMENTS OF THE PA SUBUNIT OF RNA DEPENDENT RNA POLYMERASE FROM PANDEMIC INFLUENZA VIRUS A 2009 H1N1, AND THEIR USE

机译:2009年H1N1大流行性流感病毒RNA依赖的RNA聚合酶的PA亚基片段及其用途

摘要

The present invention relates to polypeptide fragments comprising an amino-terminal fragment of the PA subunit of a viral RNA-dependent RNA polymerase possessing endonuclease activity, wherein said PA subunit is from Influenza A 2009 pandemic H1N1 virus or is a variant thereof. This invention also relates to (i) crystals of the polypeptide fragments which are suitable for structure determination of said polypeptide fragments using X-ray crystallography and (ii) computational methods using the structural coordinates of said polypeptide to screen for and design compounds that modulate, preferably inhibit the endonucleolytically active site within the polypeptide fragment. In addition, this invention relates to methods identifying compounds that bind to the PA polypeptide fragments possessing endonuclease activity and preferably inhibit said endonucleolytic activity, preferably in a high throughput setting. This invention also relates to compounds which are able to modulate, preferably to inhibit, the endonuclease activity of the PA subunit polypeptide fragment or variant thereof of the present invention and pharmaceutical compositions comprising said compounds for the treatment of disease conditions caused by viral infections with viruses of the Orthomyxoviridae family, Bunyaviridae family and/or Arenviridae family, preferably caused by viral infections with Influenza A 2009 pandemic H1N1 virus. Preferably, said compounds are identifiable by the methods disclosed herein or said pharmaceutical compositions are producible by the methods disclosed herein.
机译:本发明涉及包含具有核酸内切酶活性的病毒RNA依赖性RNA聚合酶的PA亚基的氨基末端片段的多肽片段,其中所述PA亚基来自A型流感2009大流行H1N1病毒或其变体。本发明还涉及(i)适用于使用X射线晶体学确定所述多肽片段结构的多肽片段晶体,以及(ii)使用所述多肽的结构坐标筛选和设计可调节化合物的计算方法,优选地,抑制多肽片段内的核酸内切活性位点。另外,本发明涉及鉴定与具有内切核酸酶活性的PA多肽片段结合并优选抑制所述内切核酸活性的化合物的方法,优选在高通量条件下。本发明还涉及能够调节,优选抑制本发明PA亚基多肽片段或其变体的核酸内切酶活性的化合物,以及包含所述化合物的药物组合物,用于治疗由病毒感染病毒引起的疾病正粘病毒科,布尼亚病毒科和/或戊病毒科的“人”感染,最好是由2009年甲型流感H1N1大流行病毒的病毒感染引起的。优选地,所述化合物可通过本文公开的方法鉴定或所述药物组合物可通过本文公开的方法生产。

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