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Rapid rotation of micron and submicron dielectric particles measured using optical tweezers

机译:使用光镊测量微米和亚微米介电粒子的快速旋转

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摘要

We demonstrate the use of a laser trap ('optical tweezers') and back-focal-plane position detector to measure rapid rotation in aqueous solution of single particles with sizes in the vicinity of 1 μm. Two types of rotation were measured: electrorotation of polystyrene microspheres and rotation of the flagellar motor of the bacterium Vibrio alginolyticus. In both cases, speeds in excess of 1000 Hz (rev s~(-1)) were measured. Polystyrene beads of diameter about 1 μm labelled with smaller beads were held at the centre of a microelectrode array by the optical tweezers. Electrorotation of the labelled beads was induced by applying a rotating electric field to the solution using microelectrodes. Electrorotation spectra were obtained by varying the frequency of the applied field and analysed to obtain the surface conductance of the beads. Single cells of V. alginolyticus were trapped and rotation of the polar sodium-driven flagellar motor was measured. Cells rotated more rapidly in media containing higher concentrations of Na~+, and photodamage caused by the trap was considerably less when the suspending medium did not contain oxygen. The technique allows single-speed measurements to be made in less than a second and separate particles can be measured at a rate of several per minute.
机译:我们演示了使用激光陷阱(“光学镊子”)和后焦平面位置检测器来测量尺寸在1μm附近的单个粒子在水溶液中的快速旋转。测量了两种类型的旋转:聚苯乙烯微球的电旋转和溶藻弧菌细菌的鞭毛马达的旋转。在这两种情况下,测得的速度均超过1000 Hz(rev s〜(-1))。用光镊将直径约1μm的聚苯乙烯珠(用较小的珠标记)保持在微电极阵列的中心。通过使用微电极对溶液施加旋转电场,可以使标记的珠粒发生电旋转。通过改变施加电场的频率获得电旋转光谱,并进行分析以获得珠的表面电导。捕获溶藻弧菌的单细胞并测量极性钠驱动鞭毛马达的旋转。在含有较高浓度Na +的培养基中,细胞旋转得更快,而当悬浮的培养基中不含氧气时,由阱引起的光损伤则要小得多。该技术可以在不到一秒的时间内完成单速测量,并且可以每分钟数次的速度测量单独的颗粒。

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