Förderer Moritz, Georgiev Tihomir, Mosqueira Matias, Fink Rainer H A, Vogel Martin
Medical Biophysics Unit, Institute for Physiology and Pathophysiology, University of Heidelberg, Heidelberg, Germany;
Medical Biophysics Unit, Institute for Physiology and Pathophysiology, University of Heidelberg, Heidelberg, Germany.
Biomed Opt Express. 2016 Jan 15;7(2):525-41. doi: 10.1364/BOE.7.000525. eCollection 2016 Feb 1.
Second harmonic generation (SHG) microscopy is a powerful tool for label free ex vivo or in vivo imaging, widely used to investigate structure and organization of endogenous SHG emitting proteins such as myosin or collagen. Polarization resolved SHG microscopy renders supplementary information and is used to probe different molecular states. This development towards functional SHG microscopy is calling for new methods for high speed functional imaging of dynamic processes. In this work we present two approaches with linear polarized light and demonstrate high speed line scan measurements of the molecular dynamics of the motor protein myosin with a time resolution of 1 ms in mammalian muscle cells. Such a high speed functional SHG microscopy has high potential to deliver new insights into structural and temporal molecular dynamics under ex vivo or in vivo conditions.
二次谐波产生(SHG)显微镜是一种用于离体或体内无标记成像的强大工具,广泛应用于研究内源性SHG发射蛋白(如肌球蛋白或胶原蛋白)的结构和组织。偏振分辨SHG显微镜可提供补充信息,并用于探测不同的分子状态。这种向功能性SHG显微镜的发展需要新的方法来对动态过程进行高速功能成像。在这项工作中,我们展示了两种使用线偏振光的方法,并证明了在哺乳动物肌肉细胞中以1毫秒的时间分辨率对运动蛋白肌球蛋白的分子动力学进行高速线扫描测量。这种高速功能性SHG显微镜有很大潜力在离体或体内条件下为结构和时间分子动力学提供新的见解。