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Visible Thrombolysis Acceleration of a Nanomachine Powered by Light-Driving F0F1-ATPase Motor

机译:光驱动F0F1-ATPase电机驱动的纳米机的可见溶栓加速

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摘要

We report on thrombolysis acceleration of a nanomachine powered by light-driving δ-subunit-free F0F1-ATPase motor. It is composed of a mechanical device, locating device, energy storage device, and propeller. The rotory δ-subunit-free F0F1-ATPase motor acts as a mechanical device, which was obtained by reconstructing an original chromatophore extracted from Rhodospirillum rubrum. We found that the bioactivity of the F0F1-ATPase motor improved greatly after reconstruction. The zeta potential of the nanomachine is about −23.4 mV. Cytotoxicity induced by the nanomachine was measured using cell counting kit (CCK)-8 assay. The A549 cells incubated with different fractional concentrations of the nanomachine within 48 h did not show obvious cytotoxicity. The locating device helps the nanomachine bind to the thrombi. Energy was easily stored by exposing the nanomachine to 600-nm-wavelength irradiation, which promoted activity of the motor. The rotation of the long propeller accelerated thrombolysis of a blood clot in vitro in the presence of urokinase (UK). This result was based on visual inspection and confirmed by a series of tests.Electronic supplementary materialThe online version of this article (doi:10.1186/s11671-015-0918-z) contains supplementary material, which is available to authorized users.
机译:我们报告由光驱动无δ亚基的F0F1-ATPase电机驱动的纳米机的溶栓加速。它由机械装置,定位装置,储能装置和螺旋桨组成。不含δ亚基的F0F1-ATPase转子马达是一种机械装置,它是通过重建从红螺旋藻提取的原始色谱而获得的。我们发现重建后F0F1-ATPase电机的生物活性大大提高。纳米机器的zeta电位约为-23.4 mV。使用细胞计数试剂盒(CCK)-8测定法测量由纳米机器诱导的细胞毒性。在48小时内与不同分数浓度的纳米机械一起孵育的A549细胞没有显示出明显的细胞毒性。定位装置帮助纳米机器与血栓结合。通过将纳米机械暴露于600 nm波长的辐射下,可以轻松存储能量,从而提高了电机的活动能力。在存在尿激酶(英国)的情况下,长螺旋桨的旋转加速了体外血块的血栓溶解。此结果基于目视检查并经过一系列测试确认。电子补充材料本文的在线版本(doi:10.1186 / s11671-015-0918-z)包含补充材料,授权用户可以使用。

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