Department of Biochemistry, Faculty of Life Sciences, Aligarh Muslim University, Aligarh 202002, India.
Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh 202002, India.
Int J Biol Macromol. 2018 Dec;120(Pt B):2381-2389. doi: 10.1016/j.ijbiomac.2018.09.006. Epub 2018 Sep 6.
Consumption of silver nanoparticles (AgNPs) has been increased many folds due to its antimicrobial actions resulting in its widespread incorporation into a wide range of biomedical and consumer products. Still, enough research is needed to clearly understand the effect of these nanoparticles on the conformations of important macromolecules like proteins under different pathophysiological conditions. Pointing towards the situation, we carefully designed an in vitro study to elucidate the effect of green AgNPs on the aggregation pattern of α-chymotrypsinogen A at a human pathological body temperature. We observed that the B-AgNPs inhibited the aggregation in αCgn-A in a concentration-dependent manner showing maximum inhibition at 30 μg/ml above which the effect of aggregation inhibition was reduced as evident at 40 and 50 μg/ml concentrations of B-AgNPs. Further, in our in vitro analysis, we found that the B-AgNPs of lower sizes has potential chaperone-like activity at pathological body temperature, which can be used as a component of the drug to prevent protein aggregation after further verification in animal models.
由于其抗菌作用,银纳米粒子(AgNPs)的消耗增加了许多倍,因此广泛应用于各种生物医学和消费产品中。然而,仍需要进行足够的研究,以清楚了解这些纳米粒子在不同病理生理条件下对蛋白质等重要大分子构象的影响。针对这种情况,我们精心设计了一项体外研究,以阐明绿 AgNPs 对人病理体温下α-糜蛋白酶原 A 聚集模式的影响。我们观察到,B-AgNPs 以浓度依赖的方式抑制 αCgn-A 的聚集,在 30μg/ml 以上时显示出最大抑制作用,而在 40 和 50μg/ml 的 B-AgNPs 浓度下,抑制聚集的效果降低。此外,在我们的体外分析中,我们发现较低尺寸的 B-AgNPs 在病理体温下具有潜在的分子伴侣样活性,可以作为药物的一个组成部分,在动物模型中进一步验证后,用于预防蛋白质聚集。