Yusuf Hamied Department of Chemistry, University of Cambridge, Cambridge, UK.
Aligning Science Across Parkinson's (ASAP) Collaborative Research Network, Chevy Chase, MD, USA.
Nat Methods. 2024 Oct;21(10):1873-1883. doi: 10.1038/s41592-024-02382-8. Epub 2024 Oct 7.
Current methods for single-molecule orientation localization microscopy (SMOLM) require optical setups and algorithms that can be prohibitively slow and complex, limiting widespread adoption for biological applications. We present POLCAM, a simplified SMOLM method based on polarized detection using a polarization camera, which can be easily implemented on any wide-field fluorescence microscope. To make polarization cameras compatible with single-molecule detection, we developed theory to minimize field-of-view errors, used simulations to optimize experimental design and developed a fast algorithm based on Stokes parameter estimation that can operate over 1,000-fold faster than the state of the art, enabling near-instant determination of molecular anisotropy. To aid in the adoption of POLCAM, we developed open-source image analysis software and a website detailing hardware installation and software use. To illustrate the potential of POLCAM in the life sciences, we applied our method to study α-synuclein fibrils, the actin cytoskeleton of mammalian cells, fibroblast-like cells and the plasma membrane of live human T cells.
目前的单分子取向定位显微镜(SMOLM)方法需要光学设置和算法,这些可能非常缓慢和复杂,限制了其在生物学应用中的广泛采用。我们提出了 POLCAM,这是一种基于偏振检测的简化 SMOLM 方法,使用偏振相机,可以很容易地在任何宽场荧光显微镜上实现。为了使偏振相机与单分子检测兼容,我们开发了理论来最小化视场误差,使用模拟来优化实验设计,并开发了一种基于斯托克斯参数估计的快速算法,其运行速度比现有技术快 1000 倍以上,能够近乎即时确定分子各向异性。为了帮助采用 POLCAM,我们开发了开源图像分析软件和一个网站,详细介绍了硬件安装和软件使用。为了说明 POLCAM 在生命科学中的潜力,我们将我们的方法应用于研究α-突触核蛋白纤维、哺乳动物细胞的肌动蛋白细胞骨架、成纤维样细胞和活人 T 细胞的质膜。