McArdle Laboratory for Cancer Research, Department of Oncology, University of Wisconsin-Madison , Madison, WI, USA.
Biophysics Graduate Program, University of Wisconsin-Madison , Madison, WI, USA.
J Cell Biol. 2023 Apr 3;222(4). doi: 10.1083/jcb.202202078. Epub 2023 Jan 30.
The widespread use of fluorescence microscopy has prompted the ongoing development of tools aiming to improve resolution and quantification accuracy for study of biological questions. Current calibration and quantification tools for fluorescence images face issues with usability/user experience, lack of automation, and comprehensive multidimensional measurement/correction capabilities. Here, we developed 3D-Speckler, a versatile, and high-throughput image analysis software that can provide fluorescent puncta quantification measurements such as 2D/3D particle size, spatial location/orientation, and intensities through semi-automation in a single, user-friendly interface. Integrated analysis options such as 2D/3D local background correction, chromatic aberration correction, and particle matching/filtering are also encompassed for improved precision and accuracy. We demonstrate 3D-Speckler microscope calibration capabilities by determining the chromatic aberrations, field illumination uniformity, and response to nanometer-scale emitters above and below the diffraction limit of our imaging system using multispectral beads. Furthermore, we demonstrated 3D-Speckler quantitative capabilities for offering insight into protein architectures and composition in cells.
荧光显微镜的广泛应用促使人们不断开发工具,旨在提高分辨率和定量准确性,以研究生物学问题。当前用于荧光图像的校准和定量工具在可用性/用户体验、缺乏自动化以及全面的多维测量/校正功能方面存在问题。在这里,我们开发了 3D-Speckler,这是一种通用且高通量的图像分析软件,可以通过在单个用户友好的界面中进行半自动处理,提供荧光斑点定量测量,例如 2D/3D 粒径、空间位置/方向和强度。还包括集成的分析选项,例如 2D/3D 局部背景校正、色差校正和粒子匹配/过滤,以提高精度和准确性。我们通过使用多光谱珠来确定我们成像系统的色差、场照明均匀性以及对纳米级发射器的响应,来演示 3D-Speckler 显微镜的校准能力,这些发射器在我们成像系统的衍射极限之上和之下。此外,我们还展示了 3D-Speckler 的定量能力,为深入了解细胞中的蛋白质结构和组成提供了帮助。