Deufel Christopher, Wang Michelle D
Cornell University, Department of Physics, Laboratory of Atomic and Solid State Physics, Ithaca, New York 14853, USA.
Biophys J. 2006 Jan 15;90(2):657-67. doi: 10.1529/biophysj.105.065458. Epub 2005 Oct 28.
We present measurements of the forces on, and displacements of, an optically trapped bead along the propagation direction of the trapping laser beam (the axial direction). In a typical experimental configuration, the bead is trapped in an aqueous solution using an oil-immersion, high-numerical-aperture objective. This refractive index mismatch complicates axial calibrations due to both a shift of the trap center along the axial direction and spherical aberrations. In this work, a known DNA template was unzipped along the axial direction and its characteristic unzipping force-extension data were used to determine 1), the location of the trap center along the axial direction; 2), the axial displacement of the bead from the trap center; and 3), the axial force exerted on the bead. These axial calibrations were obtained for trap center locations up to approximately 4 microm into the aqueous solution and with axial bead displacements up to approximately 600 nm from the trap center. In particular, the axial trap stiffness decreased substantially when the trap was located further into the aqueous solution. This approach, together with conventional lateral calibrations, results in a more versatile optical trapping instrument that is accurately calibrated in all three dimensions.
我们展示了沿捕获激光束传播方向(轴向)对光学捕获微珠所受的力以及微珠位移的测量结果。在典型的实验配置中,使用油浸、高数值孔径物镜将微珠捕获在水溶液中。由于捕获中心沿轴向的偏移和球差,这种折射率失配使得轴向校准变得复杂。在这项工作中,一个已知的DNA模板沿轴向解开,其特征性的解链力-伸长数据被用于确定:1)捕获中心沿轴向的位置;2)微珠相对于捕获中心的轴向位移;3)施加在微珠上的轴向力。这些轴向校准是针对捕获中心在水溶液中深入至约4微米的位置以及微珠相对于捕获中心轴向位移达约600纳米的情况获得的。特别地,当捕获中心进一步深入水溶液时,轴向捕获刚度显著降低。这种方法与传统的横向校准相结合,形成了一种在所有三个维度上都经过精确校准的更通用的光学捕获仪器。