School of Engineering and Applied Sciences, Harvard University, 33 Oxford Street, Cambridge, Massachusetts 02138, USA.
ACS Nano. 2013 Feb 26;7(2):1725-30. doi: 10.1021/nn305826j. Epub 2013 Jan 22.
An improved ability to sense particles and biological molecules is crucial for continued progress in applications ranging from medical diagnostics to environmental monitoring to basic research. Impressive electronic and photonic devices have been developed to this end. However, several drawbacks exist. The sensing of molecules is almost exclusively performed via their binding to a functionalized device surface. This means that the devices are seldom reusable, that their functionalization needs to be decided before use, and that they face the diffusion bottleneck. The latter challenge also applies to particle detection using photonic devices. Here, we demonstrate particle sensing using optical forces to trap and align them on waveguide-coupled silicon microcavities. A second probe laser detects the trapped particles by measuring the microcavity resonance shift. We also apply this platform to quantitatively sense green fluorescent proteins by detecting the size distribution of clusters of antibody-coated particles bound by the proteins.
提高对粒子和生物分子的感应能力对于从医学诊断到环境监测到基础研究等各个领域的应用的持续发展至关重要。为此已经开发出了令人印象深刻的电子和光子器件。然而,目前仍存在一些缺点。分子的感应几乎完全是通过它们与功能化器件表面的结合来实现的。这意味着这些器件很少能够重复使用,其功能化需要在使用之前确定,并且它们面临扩散瓶颈。后一个挑战也适用于使用光子器件进行粒子检测。在这里,我们使用光学力来捕获和对准它们在波导耦合的硅微腔上,展示了粒子感应。第二个探测激光通过测量微腔共振位移来检测被捕获的粒子。我们还通过检测由蛋白质结合的抗体涂层颗粒的簇的大小分布,应用该平台来定量地检测绿色荧光蛋白。