首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Three-dimensional single-molecule fluorescence imaging beyond the diffraction limit by using a double-helix point spread function
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Three-dimensional single-molecule fluorescence imaging beyond the diffraction limit by using a double-helix point spread function

机译:通过使用双螺旋点扩散函数超出衍射极限的三维单分子荧光成像

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摘要

We demonstrate single-molecule fluorescence imaging beyond the optical diffraction limit in 3 dimensions with a wide-field microscope that exhibits a double-helix point spread function (DH-PSF). The DH-PSF design features high and uniform Fisher information and has 2 dominant lobes in the image plane whose angular orientation rotates with the axial (z) position of the emitter. Single fluorescent molecules in a thick polymer sample are localized in single 500-ms acquisitions with 10- to 20-nm precision over a large depth of field (2 μm) by finding the center of the 2 DH-PSF lobes. By using a photoactivatable fluorophore, repeated imaging of sparse subsets with a DH-PSF microscope provides superresolution imaging of high concentrations of molecules in all 3 dimensions. The combination of optical PSF design and digital postprocessing with photoactivatable fluorophores opens up avenues for improving 3D imaging resolution beyond the Rayleigh diffraction limit.
机译:我们展示了一个宽分子显微镜,它显示出双螺旋点扩展功能(DH-PSF)在3维光学衍射极限以外的单分子荧光成像。 DH-PSF设计具有高且均匀的Fisher信息,并且在图像平面中具有2个主要波瓣,其角度方向随发射器的轴向(z)位置旋转。通过找到2个DH-PSF瓣的中心,可以将厚聚合物样品中的单个荧光分子以10到20纳米的精度以500毫秒的单次采集定位在较大的景深(2μm)内。通过使用可光激活的荧光团,用DH-PSF显微镜对稀疏子集进行重复成像可提供所有三个维度上高浓度分子的超分辨率成像。光学PSF设计和数字后处理与可光激活的荧光团的结合为改善3D成像分辨率(超过瑞利衍射极限)开辟了道路。

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