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Reprint of 'Accumulation of modified proteins and aggregate formation in aging'

机译:重印“老化过程中积累的修饰蛋白和聚集体”

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摘要

Increasing cellular damage during the aging process is considered to be one factor limiting the lifespan of organisms. Besides the DNA and lipids, proteins are frequent targets of non-enzymatic modifications by reactive substances including oxidants and glycating agents. Non-enzymatic protein modifications may alter the protein structure often leading to impaired functionality. Although proteolytic systems ensure the removal of modified proteins, the activity of these proteases was shown to decline during the aging process. The additional age-related increase of reactive compounds as a result of impaired antioxidant systems leads to the accumulation of damaged proteins and the formation of protein aggregates. Both, non-enzymatic modified proteins and protein aggregates impair cellular functions and tissue properties by a variety of mechanisms. This is increasingly important in aging and age-related diseases. In this review, we will give an overview on oxidation and glycation of proteins and the function of modified proteins in aggregate formation. Furthermore, their effects as well as their role in aging and age-related diseases will be highlighted. (C) 2014 Elsevier Inc. All rights reserved.
机译:在衰老过程中增加的细胞损伤被认为是限制生物寿命的因素之一。除DNA和脂质外,蛋白质通常是反应性物质(包括氧化剂和糖化剂)进行非酶修饰的目标。非酶蛋白修饰可能会改变蛋白结构,从而经常导致功能受损。尽管蛋白水解系统确保去除修饰的蛋白质,但这些蛋白酶的活性在衰老过程中显示出下降的趋势。由于抗氧化剂系统受损,与年龄相关的反应性化合物的增加会导致受损蛋白质的积累和蛋白质聚集体的形成。非酶修饰的蛋白质和蛋白质聚集体均通过多种机制损害细胞功能和组织特性。这在衰老和与年龄有关的疾病中越来越重要。在这篇综述中,我们将概述蛋白质的氧化和糖基化以及修饰的蛋白质在聚集体形成中的功能。此外,还将强调它们的作用及其在衰老和与年龄有关的疾病中的作用。 (C)2014 Elsevier Inc.保留所有权利。

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