Division of Molecular Materials Science, Graduate School of Science, Osaka City University, 3-3-138 Sugimoto, Sumiyoshi, Osaka, 5558-8585, Japan.
The OCU Advanced Research Institute for Natural Science and Technology (OCARINA), Osaka City University, 3-3-138 Sugimoto, Sumiyoshi, Osaka, 5558-8585, Japan.
Sci Rep. 2020 Feb 25;10(1):3349. doi: 10.1038/s41598-020-60165-5.
We demonstrate the size-dependent separation and permanent immobilization of DNA on plasmonic substrates by means of plasmonic optical tweezers. We found that a gold nanopyramidal dimer array enhanced the optical force exerted on the DNA, leading to permanent immobilization of the DNA on the plasmonic substrate. The immobilization was realized by a combination of the plasmon-enhanced optical force and the thermophoretic force induced by a photothermal effect of the plasmons. In this study, we applied this phenomenon to the separation and fixation of size-different DNA. During plasmon excitation, DNA strands of different sizes became permanently immobilized on the plasmonic substrate forming micro-rings of DNA. The diameter of the ring was larger for longer DNA (in base pairs). When we used plasmonic optical tweezers to trap DNA of two different lengths dissolved in solution (φx DNA (5.4 kbp) and λ-DNA (48.5 kbp), or φx DNA and T4 DNA (166 kbp)), the DNA were immobilized, creating a double micro-ring pattern. The DNA were optically separated and immobilized in the double ring, with the shorter sized DNA and the larger one forming the smaller and larger rings, respectively. This phenomenon can be quantitatively explained as being due to a combination of the plasmon-enhanced optical force and the thermophoretic force. Our plasmonic optical tweezers open up a new avenue for the separation and immobilization of DNA, foreshadowing the emergence of optical separation and fixation of biomolecules such as proteins and other ncuelic acids.
我们通过等离子体光学镊子展示了等离子体衬底上 DNA 的尺寸依赖性分离和永久固定。我们发现金纳米金字塔二聚体阵列增强了对 DNA 的光力,导致 DNA 永久固定在等离子体衬底上。这种固定是通过等离子体增强的光力和等离子体光热效应引起的热泳力的结合实现的。在这项研究中,我们将这种现象应用于不同尺寸 DNA 的分离和固定。在等离子体激发期间,不同大小的 DNA 链在等离子体衬底上永久固定,形成 DNA 的微环。对于较长的 DNA(碱基对),环的直径较大。当我们使用等离子体光学镊子捕获溶解在溶液中的两种不同长度的 DNA(φx DNA(5.4 kbp)和 λ-DNA(48.5 kbp),或 φx DNA 和 T4 DNA(166 kbp))时,DNA 被固定,形成双微环图案。DNA 被光学分离并固定在双环中,较短的 DNA 和较长的 DNA 分别形成较小和较大的环。这种现象可以定量解释为等离子体增强的光力和热泳力的结合。我们的等离子体光学镊子为 DNA 的分离和固定开辟了新途径,预示着蛋白质和其他核酸等生物分子的光学分离和固定的出现。