Department of Chemistry, Duke University, Durham, NC 27708, USA.
Molecules. 2019 Aug 2;24(15):2826. doi: 10.3390/molecules24152826.
Single molecule fluorescence spectroscopy has been largely implemented using methods which require tethering of molecules to a substrate in order to make high temporal resolution measurements. However, the act of tethering a molecule requires that the molecule be removed from its environment. This is especially perturbative when measuring biomolecules such as enzymes, which may rely on the non-equilibrium and crowded cellular environment for normal function. A method which may be able to un-tether single molecule fluorescence spectroscopy is real-time 3D single particle tracking (RT-3D-SPT). RT-3D-SPT uses active feedback to effectively lock-on to freely diffusing particles so they can be measured continuously with up to photon-limited temporal resolution over large axial ranges. This review gives an overview of the various active feedback 3D single particle tracking methods, highlighting specialized detection and excitation schemes which enable high-speed real-time tracking. Furthermore, the combination of these active feedback methods with simultaneous live-cell imaging is discussed. Finally, the successes in real-time 3D single molecule tracking (RT-3D-SMT) thus far and the roadmap going forward for this promising family of techniques are discussed.
单分子荧光光谱学在很大程度上采用了需要将分子连接到基底上的方法,以便进行高时间分辨率的测量。然而,将分子连接到基底上的过程需要将分子从其环境中取出。当测量酶等生物分子时,这种操作尤其具有干扰性,因为酶的正常功能可能依赖于非平衡和拥挤的细胞环境。一种可能能够解开单分子荧光光谱学束缚的方法是实时 3D 单粒子跟踪(RT-3D-SPT)。RT-3D-SPT 使用主动反馈来有效地锁定自由扩散的粒子,以便在大轴向范围内以光子限制的时间分辨率连续测量它们。本综述概述了各种主动反馈 3D 单粒子跟踪方法,重点介绍了能够实现高速实时跟踪的特殊检测和激发方案。此外,还讨论了这些主动反馈方法与同时进行的活细胞成像的结合。最后,讨论了实时 3D 单分子跟踪(RT-3D-SMT)迄今为止的成功,以及该技术领域未来的发展方向。