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像差单分子发射模式的测量精度界限。

Measurement precision bounds on aberrated single-molecule emission patterns.

作者信息

Fang Li, Huang Fang

出版信息

Opt Express. 2024 Aug 26;32(18):31431-31447. doi: 10.1364/OE.527267.

Abstract

Single-molecule localization microscopy (SMLM) has revolutionized the study of biological phenomena by providing exquisite nanoscale spatial resolution. However, optical aberrations induced by sample and system imperfections distort the single-molecule emission patterns (i.e. PSFs), leading to reduced precision and resolution of SMLM, particularly in three-dimensional (3D) applications. While various methods, both analytical and instrumental, have been employed to mitigate these aberrations, a comprehensive analysis of how different types of commonly encountered aberrations affect single-molecule experiments and their image formation remains missing. In this study, we addressed this gap by conducting a quantitative study of the theoretical precision limit for position and wavefront distortion measurements in the presence of aberrations. Leveraging Fisher information and Cramér-Rao lower bound (CRLB), we quantitively analyzed and compared the effects of different aberration types, including index mismatch aberrations, on localization precision in both biplane and astigmatism 3D modalities as well as 2D SMLM imaging. Furthermore, we studied the achievable wavefront estimation precision from aberrated single-molecule emission patterns, a pivot step for successful adaptive optics in SMLM through thick specimens. This analysis lays a quantitative foundation for the development and application of SMLM in whole-cells, tissues and with a large field of view, providing in-depth insights into the behavior of different aberration types in single-molecule imaging and thus generating theoretical guidelines for developing highly efficient aberration correction strategies and enhancing the precision and reliability of 3D SMLM.

摘要

单分子定位显微镜(SMLM)通过提供极高的纳米级空间分辨率,彻底改变了生物学现象的研究。然而,由样品和系统缺陷引起的光学像差会扭曲单分子发射模式(即点扩散函数),导致SMLM的精度和分辨率降低,特别是在三维(3D)应用中。虽然已经采用了各种分析和仪器方法来减轻这些像差,但对于不同类型的常见像差如何影响单分子实验及其成像形成,仍缺乏全面的分析。在本研究中,我们通过对存在像差时位置和波前畸变测量的理论精度极限进行定量研究,填补了这一空白。利用费舍尔信息和克拉美-罗下限(CRLB),我们定量分析并比较了不同像差类型(包括折射率失配像差)对双平面和像散3D模式以及2D SMLM成像中定位精度的影响。此外,我们研究了从像差单分子发射模式中可实现的波前估计精度,这是通过厚样品在SMLM中成功实现自适应光学的关键步骤。该分析为SMLM在全细胞、组织和大视野中的开发和应用奠定了定量基础,深入了解了不同像差类型在单分子成像中的行为,从而为开发高效像差校正策略以及提高3D SMLM的精度和可靠性提供了理论指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7386/11595290/caef341d700f/oe-32-18-31431-g001.jpg

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