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A super-resolution imaging method, device and terminal equipment

A technology of super-resolution imaging and super-resolution images, which is applied in the field of image processing and can solve problems such as functional super-resolution imaging and super-resolution imaging.

Active Publication Date: 2021-03-30
SHENZHEN UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The main purpose of the present invention is to propose a super-resolution imaging method, device and terminal equipment to solve the problem that the prior art can only perform super-resolution imaging on the structure of biological samples, but cannot perform functional super-resolution imaging or super-resolution imaging of sample parameters. Resolution Imaging Research Questions

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  • A super-resolution imaging method, device and terminal equipment
  • A super-resolution imaging method, device and terminal equipment
  • A super-resolution imaging method, device and terminal equipment

Examples

Experimental program
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Embodiment 1

[0063] like figure 1 As shown, the embodiment of the present invention provides a super-resolution imaging method, which can be applied to super-resolution positioning imaging of an optical reconstruction microscope, which includes:

[0064] S101. Using the excitation light, excite the fluorescent probe with double emission peaks on the biological sample, and act on the excited fluorescent probe with an affinity reagent.

[0065] In the above step S101, after the fluorescent probe with dual emission peaks is excited, two emission peaks will be displayed in the fluorescence emission spectrum of the fluorescent probe, namely a short-wavelength emission peak and a long-wavelength emission peak.

[0066] In specific applications, before the excitation light acts on the biological sample, it should also pass through optical processing elements, such as lenses, field diaphragms, tube mirrors, objective lenses, etc., so that the excitation light can be uniformly and concentratedly ir...

Embodiment 2

[0094] like figure 2 As shown, the embodiment of the present invention exemplarily shows a detailed implementation process of S102 in the first embodiment above, where step S102 is:

[0095] S102, irradiating the fluorescent probe after the affinity reagent has been acted on by activating light to obtain a dual-channel fluorescence intensity image.

[0096] Its detailed implementation process includes:

[0097] S1021. Obtain the short-wavelength signal according to the first structure in the fluorescent probe.

[0098] S1022. Obtain the long-wavelength signal according to the second structure in the fluorescent probe.

[0099] In the above step S1021 and step S1022, the wavelength of the activation light is the same as the wavelength of the excitation light, wherein the short wavelength emission peak is caused by the first structure in the probe, and the long wavelength emission peak is caused by the second structure in the probe, And the fluorescence emission spectra of t...

Embodiment 3

[0108] like Figure 4 As shown, the embodiment of the present invention exemplarily shows a detailed implementation process of step S103 in the first embodiment above, where step S103 is:

[0109] S103. Separately collect short-wavelength signals of short-wavelength emission peaks and long-wavelength signals of long-wavelength emission peaks in the dual-channel fluorescence intensity image.

[0110] Its detailed implementation process includes:

[0111] S1031. Separate the excitation light from the short-wavelength signal and the long-wavelength signal by using a first dichroic mirror.

[0112] In the above step S1031, the dichroic mirror almost completely transmits light of a certain wavelength, and almost completely reflects light of other wavelengths.

[0113] In a specific application, after the excitation light acts on the biological sample, the light emitted by the fluorescent probe on the biological sample includes a short-wavelength signal, a long-wavelength signal, ...

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Abstract

The invention is applicable to the technical field of image processing, and provides a super-resolution imaging method, a device and a terminal device. The method comprises the steps of: exciting a fluorescent probe with double emission peaks on a biological sample through excitation lights, and applying an affinity reagent to the fluorescent probe after excitation; irradiating the fluorescence probe after being treated by the affinity reagent through activating lights to obtain a two-channel fluorescence intensity image; correspondingly collecting a short-wavelength signal of a short-wavelength emission peak and a long wavelength of a long-wavelength emission peak in two-channel fluorescence intensity images; selecting N-frame two-channel fluorescence intensity images, and correspondinglycalculating the fluorescence intensity ratios of the short-wavelength signal and the long-wavelength signal to obtain N proportional fluorescence images; obtaining super-resolution images through a STORM super-resolution imaging method; and obtaining proportional super-resolution images, according to N proportional fluorescence images coloring the super-resolution images. The super-resolution imaging method, the device and the terminal device can obtain the proportional super-resolution images, and reflect sample parameters at fluorescent probe marks in biological samples.

Description

technical field [0001] The present invention relates to the technical field of image processing, in particular to a super-resolution imaging method, device and terminal equipment. Background technique [0002] Fluorescence microscopy is widely used in cellular and microbial imaging, among which super-resolution localization imaging is a representative super-resolution fluorescence imaging technique. On the basis of optical reconstruction microscopy, this technology combines single-molecule imaging with high-precision molecular positioning algorithms to achieve ultra-high spatial resolution of 20-30nm to observe the ultrastructure in cells. The key of this technique is to use the fluorescent probe in the excited state to randomly combine with the affinity reagent in the surrounding environment, causing its fluorescence to decay into a dark state, and then use another wavelength or the same wavelength of activating light to make the affinity reagent from the fluorescent molecu...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N21/64
CPCG01N21/6402G01N21/6428G01N21/6486
Inventor 杨志刚刘毋凡屈军乐
Owner SHENZHEN UNIV