Department of Biological Sciences, Columbia University, New York, NY, 10027, USA.
Current address: Department of Physics, University of Wisconsin, Milwaukee, WI, 53211, USA.
Angew Chem Int Ed Engl. 2017 Aug 7;56(33):9741-9746. doi: 10.1002/anie.201703630. Epub 2017 May 19.
A hallmark of tissue ageing is the irreversible oxidative modification of its proteins. We show that single proteins, kept unfolded and extended by a mechanical force, undergo accelerated ageing in times scales of minutes to days. A protein forced to be continuously unfolded completely loses its ability to contract by folding, becoming a labile polymer. Ageing rates vary among different proteins, but in all cases they lose their mechanical integrity. Random oxidative modification of cryptic side chains exposed by mechanical unfolding can be slowed by the addition of antioxidants such as ascorbic acid, or accelerated by oxidants. By contrast, proteins kept in the folded state and probed over week-long experiments show greatly reduced rates of ageing. We demonstrate a novel approach whereby protein ageing can be greatly accelerated: the constant unfolding of a protein for hours to days is equivalent to decades of exposure to free radicals under physiological conditions.
组织老化的一个标志是其蛋白质发生不可逆转的氧化修饰。我们表明,在几分钟到几天的时间尺度内,通过机械力保持展开和延伸的单一蛋白质会加速老化。一种被迫持续展开的蛋白质完全失去了通过折叠收缩的能力,变成了不稳定的聚合物。不同蛋白质的老化速度不同,但在所有情况下,它们都会失去机械完整性。通过机械展开暴露的隐匿侧链的随机氧化修饰可以通过添加抗坏血酸等抗氧化剂来减缓,或者通过氧化剂来加速。相比之下,保持折叠状态并在长达一周的实验中进行探测的蛋白质显示出大大降低的老化速度。我们展示了一种新的方法,通过这种方法可以大大加速蛋白质的老化:将蛋白质持续展开数小时到数天,相当于在生理条件下暴露于自由基数十年。