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UV-irradiated α-crystallin 抗聚集活性的定量分析。

Quantification of anti-aggregation activity of UV-irradiated α-crystallin.

机构信息

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.

出版信息

Int J Biol Macromol. 2015 Feb;73:84-91. doi: 10.1016/j.ijbiomac.2014.10.060. Epub 2014 Nov 18.

Abstract

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.

摘要

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。

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