Bach Institute of Biochemistry, Russian Academy of Sciences, Leninsky pr. 33, Moscow 119071, Russia.
Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, Kosygin str. 4, Moscow 119991, Russia.
Int J Biol Macromol. 2015 Feb;73:84-91. doi: 10.1016/j.ijbiomac.2014.10.060. Epub 2014 Nov 18.
Ultraviolet radiation is a risk factor for cataractogenesis. It is believed that enhanced rates of lens opacification and cataract formation are the results of gradual loss of chaperone-like efficiency of α-crystallin upon exposure to UV light. To characterize chaperone-like activity of α-crystallin damaged by UV irradiation, a test system based on dithiothreitol-induced aggregation of holo-α-lactalbumin from bovine milk was used. The adsorption capacity of α-crystallin (AC0) with respect to the target protein (α-lactalbumin) was used as a measure of anti-aggregation activity of α-crystallin. The data on SDS-PAGE testify that UV irradiation of α-crystallin results in covalent cross-linking of subunits in α-crystallin oligomers. The dependence of AC0 value on the irradiation dose was compared with the UV-induced diminution of the portion of native α-crystallin estimated from the data on differential scanning calorimetry. On the basis of such comparison a conclusion has been made that the loss in chaperone-like activity is mainly due to UV-induced denaturation of α-crystallin subunits. Cross-linking of remaining native subunits leads to an additional decrease in anti-aggregation activity.
紫外线辐射是白内障形成的一个危险因素。据认为,在暴露于紫外线下时,晶状体混浊和白内障形成的速度加快,是由于伴侣样α-晶状体蛋白逐渐丧失效率所致。为了描述紫外线照射破坏的α-晶状体蛋白的伴侣样活性,使用了基于二硫苏糖醇诱导的牛乳全α-乳白蛋白聚集的测试系统。α-晶状体蛋白(AC0)对靶蛋白(α-乳白蛋白)的吸附能力被用作α-晶状体蛋白抗聚集活性的度量。SDS-PAGE 数据证明,紫外线照射α-晶状体蛋白会导致α-晶状体蛋白寡聚物中亚基的共价交联。将 AC0 值与从差示扫描量热法数据估计的天然α-晶状体蛋白部分的 UV 诱导减少进行比较。基于这种比较得出结论,伴侣样活性的丧失主要是由于α-晶状体蛋白亚基的 UV 诱导变性。剩余天然亚基的交联导致抗聚集活性的进一步降低。