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MODIFIED CATALASE PROTEINS USEFUL FOR PROMOTION OF PEROXISOMAL CATALASE FUNCTION IN CELLS

机译:改进的过氧化氢酶蛋白,可促进细胞中过氧化物酶的过氧化氢酶功能

摘要

The molecular mechanisms of peroxisome biogenesis have begun to emerge: in contrast, relatively little is known about how the organelle functions as cells age. The present inventors characterized age-related changes in peroxisomes of human cells and showed that aging compromises peroxisomal targeting signal 1 (PTS 1) protein import, with the critical antioxidant enzyme, catalase, especially affected. The number and appearance of peroxisomes are altered in these cells, and the organelles accumulate the PTS1-import receptor, Pex5p, on their membranes. Concomitantly, cells produce increasing amounts of the toxic metabolite, H2O2, and this increased load of reactive oxygen species (ROS) may further reduce peroxisomal protein import and exacerbate the effects of aging. Disclosed are novel compositions and methods for restoring catalase in peroxisomes by use of targeted catalase modified at its C-terminus and/or N-terminus, optionally in combination with polypeptides which promote cellular uptake of proteins, to prevent or overcome the changes that follows aging or that are associated with a number of diseases or disorders.
机译:过氧化物酶体生物发生的分子机制已经开始出现:相反,关于细胞器如何随着细胞衰老起作用的信息知之甚少。本发明人表征了人类细胞的过氧化物酶体中与年龄相关的变化,并表明老化损害了过氧化物酶体靶向信号1(PTS 1)蛋白的导入,特别是影响了关键的抗氧化酶过氧化氢酶。这些细胞中过氧化物酶体的数量和外观发生了变化,细胞器在其膜上积聚了PTS1导入受体Pex5p。同时,细胞产生越来越多的有毒代谢产物H2O2,而这种增加的活性氧(ROS)负荷可能会进一步减少过氧化物酶体蛋白的导入,并加剧衰老的影响。公开了新颖的组合物和方法,其通过使用在其C末端和/或N末端修饰的靶向过氧化氢酶,任选地与促进蛋白质摄取细胞的多肽组合,以预防或克服衰老后的变化,从而在过氧化物酶体中恢复过氧化氢酶或与多种疾病或失调有关。

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