Department of Health Technology, Technical University of Denmark (DTU), Kongens Lyngby 2800, Denmark.
Department of Applied Physics and Science Education, Eindhoven University of Technology (TU/e), Eindhoven 5600 MB, The Netherlands.
ACS Nano. 2024 Oct 29;18(43):29832-29845. doi: 10.1021/acsnano.4c09719. Epub 2024 Oct 16.
Nanoparticles (NPs) have proven their applicability in biosensing, drug delivery, and photothermal therapy, but their performance depends critically on the distribution and number of functional groups on their surface. When studying surface functionalization using super-resolution microscopy, the NP modifies the fluorophore's point-spread function (PSF). This leads to systematic mislocalizations in conventional analyses employing Gaussian PSFs. Here, we address this shortcoming by deriving the analytical PSF model for a fluorophore near a spherical NP. Its calculation is four orders of magnitude faster than numerical approaches and thus feasible for direct use in localization algorithms. We fit this model to individual 2D images from DNA-PAINT experiments on DNA-coated gold NPs and demonstrate extraction of the 3D positions of functional groups with <5 nm precision, revealing inhomogeneous surface coverage. Our method is exact, fast, accessible, and poised to become the standard in super-resolution imaging of NPs for biosensing and drug delivery applications.
纳米粒子(NPs)已被证明在生物传感、药物输送和光热治疗方面具有适用性,但它们的性能取决于其表面上功能基团的分布和数量。在使用超分辨率显微镜研究表面功能化时,NP 会改变荧光团的点扩散函数(PSF)。这会导致在使用高斯 PSF 的常规分析中出现系统的定位错误。在这里,我们通过推导荧光团附近球形 NP 的解析 PSF 模型来解决这个问题。与数值方法相比,它的计算速度快四个数量级,因此可以直接用于定位算法。我们将该模型拟合到 DNA 涂覆金 NPs 上的 DNA-PAINT 实验的单个 2D 图像上,并证明可以以小于 5nm 的精度提取功能基团的 3D 位置,从而揭示出不均匀的表面覆盖度。我们的方法是精确的、快速的、易于使用的,并且有望成为生物传感和药物输送应用中纳米粒子超分辨率成像的标准方法。