Dartmouth College, Thayer School of Engineering, 8000 Cummings Hall, Hanover, New Hampshire 03755, USA.
Langmuir. 2010 Jul 20;26(14):12003-11. doi: 10.1021/la1015252.
Force spectroscopy based on magnetic tweezers is a powerful technique for manipulating single biomolecules and studying their interactions. The resolution in magnetic probe displacement, however, needs to be commensurate with molecular sizes. To achieve the desirable sensitivity in tracking displacements of the magnetic probe, some recent approaches have combined magnetic tweezers with total internal reflection fluorescence microscopy. In this situation, a typical force probe is a polymer microsphere containing two types of optically active components: a pure absorber (magnetic nanoparticles for providing the pulling force) and a luminophore (semiconducting nanoparticles or organic dyes for fluorescent imaging). To assess the system's capability fully with regard to tracking the position of the force probe with subnanometer accuracy, we developed a body-of-revolution formulation of the method of auxiliary sources (BOR-MAS) to simulate the absorption, scattering, and fluorescence of microscopic spheres in an evanescent electromagnetic field. The theoretical formulation uses the axial symmetry of the system to reduce the dimensionality of the modeling problem and produces excellent agreement with the reported experimental data on forward scattering intensity. Using the BOR-MAS numerical model, we investigated the probe detection sensitivity for a high numerical aperture objective. The analysis of both backscattering and fluorescence observation modes shows that the total intensity of the bead image decays exponentially with the distance from the surface (or the length of a biomolecule). Our investigations demonstrate that the decay lengths of observable optical power are smaller than the penetration depth of the unperturbed excitation evanescent wave. In addition, our numerical modeling results illustrate that the expected sensitivity for the decay length changes with the angle of incidence, tracking the theoretical penetration depth for a two-media model, and is sensitive to the bead size. The BOR-MAS methodology developed in this work for near-field modeling of bead-tracking experiments fully describes the fundamental photonic response of microscopic BOR probes at the subwavelength level and can be used for future improvements in the design of these probes or in the setup of bead-tracking experiments.
基于磁镊的力谱学是一种操纵单个生物分子并研究它们相互作用的强大技术。然而,磁探针位移的分辨率需要与分子尺寸相匹配。为了在跟踪磁探针位移时获得所需的灵敏度,一些最近的方法将磁镊与全内反射荧光显微镜相结合。在这种情况下,典型的力探针是一种含有两种光学活性成分的聚合物微球:纯吸收剂(用于提供拉力的磁性纳米粒子)和发光体(半导体纳米粒子或有机染料用于荧光成像)。为了充分评估系统以亚纳米精度跟踪力探针位置的能力,我们开发了一种辅助源的旋转体公式(BOR-MAS)来模拟在渐逝电磁场中微观球体的吸收、散射和荧光。理论公式利用系统的轴对称性降低了建模问题的维数,并与报告的关于前向散射强度的实验数据非常吻合。使用 BOR-MAS 数值模型,我们研究了高数值孔径物镜的探针检测灵敏度。对背散射和荧光观察模式的分析表明,微球图像的总强度随距表面的距离(或生物分子的长度)呈指数衰减。我们的研究表明,可观察光学功率的衰减长度小于未扰动激发渐逝波的穿透深度。此外,我们的数值模拟结果表明,衰减长度变化的预期灵敏度随入射角而变化,跟踪双介质模型的理论穿透深度,并且对球的大小敏感。这项工作中为近场微球跟踪实验建模开发的 BOR-MAS 方法充分描述了亚波长水平微观 BOR 探针的基本光子响应,并可用于未来改进这些探针的设计或微球跟踪实验的设置。