Pico-liter injection control to individual nano-liter solution coated by lipid layer

Y. Matsuno, M. Nakajima, M. Kojima, Y. Tanaka-Takiguchi, K. Takiguchi, K. Nogawa, M. Homma, T. Fukuda
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引用次数: 3

Abstract

This paper presents the evaluation of ultra-minimal spout amount from micro-nano pipettes into phospholipid-coated micro-droplets. The pipettes can be used to control the local environment around/inside single cells. Conventionally, the microinjection with pipette has been conducted by air pressures. In this method, the spout of high viscosity solutions is difficult because of the frictional forces between the surface of a pipette and a solution. It is also needed to evaluate the spout amount quantitatively. On the other hand, the research about artificial cell model has been actively conducted, injecting various biological samples into liposomes which are vesicle of lipid bilayer membrane. If additional injection of various proteins into liposome is realized with micro/nano pipette, the observation of dynamic reaction of multiple biological samples, which is required for formulation of artificial cell, will become possible. In our research, the spouting method using electro-osmosis is used. The local spouts of the proteins such as GFP and F-actin have been presented experimentally before. In this paper, the amount of spout solution in this method is quantitatively evaluated by injection of fluorescent solution into a phospholipid-coated micro-droplet.
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微升注射控制到单个纳升溶液涂有脂质层
本文介绍了从微纳移液器到磷脂包被微液滴的超最小喷出量的评价。移液器可用于控制单个细胞周围/内部的局部环境。传统上,用移液管进行显微注射是在气压下进行的。在这种方法中,由于移液管表面和溶液之间的摩擦力,高粘度溶液的喷射是困难的。还需要定量地评价喷淋量。另一方面,积极开展人工细胞模型的研究,将各种生物样品注射到脂质体中,脂质体是脂质双层膜的囊泡。如果用微纳移液器实现脂质体中各种蛋白的附加注射,就可以观察多种生物样品的动态反应,这是制备人工细胞所需要的。在我们的研究中,采用电渗透的喷射方法。GFP和f -肌动蛋白等蛋白的局部喷口已经在实验中被发现。本文通过将荧光溶液注射到磷脂包被的微滴中,定量地评价了该方法的喷液量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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