Department of Physics and Astronomy , Michigan State University , East Lansing , Michigan 48824 , United States.
J Phys Chem A. 2019 Nov 7;123(44):9612-9620. doi: 10.1021/acs.jpca.9b08282. Epub 2019 Oct 28.
We present an instrument that combines high-resolution optical tweezers and multicolor confocal fluorescence spectroscopy along with automated single-molecule assembly. The multicolor allows the simultaneous observation of multiple molecules or multiple degrees of freedom, which allows, for example, the observation of multiple proteins simultaneously within a complex. The instrument incorporates three fluorescence excitation lasers, with a reliable alignment scheme, which will allow three independent fluorescent probe or FRET measurements and also increases flexibility in the choice of fluorescent molecules. We demonstrate the ability to simultaneously measure angstrom-scale changes in tether extension and fluorescence signals. Simultaneous tweezers and fluorescence measurement are particularly challenging because of fluorophore photobleaching, even more so if multiple fluorophores are to be measured. Therefore, (1) fluorescence excitation and detection is interlaced with time-shared dual optical traps. (2) We investigated the photostability of common fluorophores. The mean number of photons emitted before bleaching was unaffected by the trap laser and decreased only slightly with increasing excitation laser intensity. Surprisingly, we found that Cy5 outperforms other commonly used fluorophores by more than fivefold. (3) We devised computer-controlled automation, which conserves fluorophore lifetime by quickly detecting fluorophore-labeled molecule binding, turning off lasers, and moving to add the next fluorophore-labeled component. The single-molecule assembly line enables the precise assembly of multimolecule complexes while preserving fluorophores.
我们展示了一种仪器,它结合了高分辨率光镊和多色共焦荧光光谱学,以及自动化的单分子组装。多色共焦允许同时观察多个分子或多个自由度,例如,可以同时观察复杂体系中的多个蛋白质。该仪器包含三个荧光激发激光器,具有可靠的对准方案,这将允许进行三个独立的荧光探针或 FRET 测量,并增加了对荧光分子选择的灵活性。我们展示了同时测量连接延伸和荧光信号的埃级变化的能力。由于荧光团的光漂白,同时进行光镊和荧光测量特别具有挑战性,如果要测量多个荧光团则更是如此。因此,(1)荧光激发和检测与分时双光阱交错进行。(2)我们研究了常见荧光团的光稳定性。在漂白之前发射的平均光子数不受陷阱激光的影响,仅随激发激光强度的增加而略有下降。令人惊讶的是,我们发现 Cy5 的性能比其他常用荧光团好五倍以上。(3)我们设计了计算机控制的自动化系统,通过快速检测荧光标记分子的结合,关闭激光器,并移动以添加下一个荧光标记组件,从而延长荧光团的寿命。单分子组装线能够在保留荧光团的同时精确组装多分子复合物。