Eyer Klaus, Kuhn Phillip, Stratz Simone, Dittrich Petra S
Department of Chemistry and Applied Biosciences, ETH Zurich, Switzerland.
J Vis Exp. 2013 Oct 15(80):e50618. doi: 10.3791/50618.
We present a microfluidic device that enables the quantitative determination of intracellular biomolecules in multiple single cells in parallel. For this purpose, the cells are passively trapped in the middle of a microchamber. Upon activation of the control layer, the cell is isolated from the surrounding volume in a small chamber. The surrounding volume can then be exchanged without affecting the isolated cell. However, upon short opening and closing of the chamber, the solution in the chamber can be replaced within a few hundred milliseconds. Due to the reversibility of the chambers, the cells can be exposed to different solutions sequentially in a highly controllable fashion, e.g. for incubation, washing, and finally, cell lysis. The tightly sealed microchambers enable the retention of the lysate, minimize and control the dilution after cell lysis. Since lysis and analysis occur at the same location, high sensitivity is retained because no further dilution or loss of the analytes occurs during transport. The microchamber design therefore enables the reliable and reproducible analysis of very small copy numbers of intracellular molecules (attomoles, zeptomoles) released from individual cells. Furthermore, many microchambers can be arranged in an array format, allowing the analysis of many cells at once, given that suitable optical instruments are used for monitoring. We have already used the platform for proof-of-concept studies to analyze intracellular proteins, enzymes, cofactors and second messengers in either relative or absolute quantifiable manner.
我们展示了一种微流控装置,该装置能够并行定量测定多个单细胞内的生物分子。为此,细胞被被动捕获在微腔室的中间。激活控制层后,细胞在一个小腔室中与周围的液体隔离开来。然后可以更换周围的液体,而不影响被隔离的细胞。然而,在腔室短暂打开和关闭时,腔室内的溶液可以在几百毫秒内被替换。由于腔室的可逆性,细胞可以以高度可控的方式依次暴露于不同的溶液中,例如用于孵育、洗涤,最后进行细胞裂解。紧密密封的微腔室能够保留裂解液,在细胞裂解后将稀释降至最低并加以控制。由于裂解和分析在同一位置进行,因此能保持高灵敏度,因为在运输过程中分析物不会进一步稀释或损失。因此,微腔室设计能够可靠且可重复地分析从单个细胞释放的极低拷贝数的细胞内分子(阿托摩尔、zeptomoles)。此外,如果使用合适的光学仪器进行监测,许多微腔室可以排列成阵列形式,从而能够同时分析多个细胞。我们已经将该平台用于概念验证研究,以相对或绝对可量化的方式分析细胞内蛋白质、酶、辅因子和第二信使。