Honisch Claudia, Donadello Viola, Hussain Rohanah, Peterle Daniele, De Filippis Vincenzo, Arrigoni Giorgio, Gatto Claudio, Giurgola Laura, Siligardi Giuliano, Ruzza Paolo
Institute of Biomolecular Chemistry of CNR, Padua Unit, 35131 Padova, Italy.
Department of Chemical Sciences, University of Padova, 35131 Padova, Italy.
ACS Omega. 2020 Feb 17;5(8):4293-4301. doi: 10.1021/acsomega.9b04234. eCollection 2020 Mar 3.
The eye lens is mainly composed of the highly ordered water-soluble (WS) proteins named crystallins. The aggregation and insolubilization of these proteins lead to progressive lens opacification until cataract onset. Although this is a well-known disease, the mechanism of eye lens protein aggregation is not well understood; however, one of the recognized causes of proteins modification is related to the exposure to UV light. For this reason, the spectroscopic properties of WS lens proteins and their stability to UV irradiation have been evaluated by different biophysical methods including synchrotron radiation circular dichroism, fluorescence, and circular dichroism spectroscopies. Moreover, dynamic light scattering, gel electrophoresis, transmission electron microscopy, and protein digestion followed by tandem LC-MS/MS analysis were used to study the morphological and structural changes in protein aggregates induced by exposure to UV light. Our results clearly indicated that the exposure to UV radiation modified the protein conformation, inducing a loss of ordered structure and aggregation. Furthermore, we confirmed that these changes were attributable to the generation of reactive oxygen species due to the irradiation of the protein sample. This approach, involving the photodenaturation of proteins, provides a benchmark in high-throughput screening of small molecules suitable to prevent protein denaturation and aggregation.
眼球晶状体主要由名为晶状体蛋白的高度有序的水溶性(WS)蛋白质组成。这些蛋白质的聚集和不溶性导致晶状体逐渐浑浊直至白内障发作。尽管这是一种众所周知的疾病,但眼球晶状体蛋白聚集的机制尚未完全了解;然而,公认的蛋白质修饰原因之一与暴露于紫外线下有关。因此,已通过不同的生物物理方法,包括同步辐射圆二色性、荧光和圆二色性光谱,评估了WS晶状体蛋白的光谱特性及其对紫外线照射的稳定性。此外,动态光散射、凝胶电泳、透射电子显微镜以及蛋白质消化后进行串联液相色谱-串联质谱分析,用于研究暴露于紫外线下引起的蛋白质聚集体的形态和结构变化。我们的结果清楚地表明,暴露于紫外线辐射会改变蛋白质构象,导致有序结构丧失和聚集。此外,我们证实这些变化归因于蛋白质样品照射产生的活性氧。这种涉及蛋白质光变性的方法为适合预防蛋白质变性和聚集的小分子高通量筛选提供了一个基准。