Microfluidics-based automatic immunofluorescence staining for single-molecule localization microscopy

Full automation of single-molecule localization microscopy (SMLM) is crucial for large-scale and high-throughput cellular imaging. It is well-known that SMLM typically consists of three major steps: immunofluorescence (IF) staining, optical imaging, and image processing. Currently, automation in optical imaging and image processing is almost complete; however, the automation of IF staining has been slow to advance, probably due to its complicated experimental operations. Here we present a low-cost automated method for IF staining, called super-resolution immunofluorescence staining by microfluidics (SRIF-fluidics). This method is suitable for both adherent and suspension cells and supports single-color and multi-color IF staining for SMLM. Our results show that SRIF-fluidics reduces antibody consumption by about 75% and shortens the sample preparation time from 5.6 hours (manual operation) to 2.5 ∼ 4.4 hours, depending on the sample types. Importantly, this method provides a satisfactory consistency of imaging results without sacrificing sample labeling quality. We believe that the method proposed in this paper is a necessary supplement to achieving fully automated SMLM and facilitating high-throughput SMLM in the near future.

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Publication Details

Journal
Biomedical Optics Express
Published
2024-11-05
DOI
https://doi.org/10.1364/boe.540434
Citations
1
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
0.66

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article

Microfluidics-based automatic immunofluorescence staining for single-molecule localization microscopy

Weibing Kuang, Jun Dong, Zhen‐Li Huang, Bing Shi
1 citations
Biomedical Optics Express
Advanced Fluorescence Microscopy Techniques
0.66
article

Microfluidics-based automatic immunofluorescence staining for single-molecule localization microscopy

Weibing Kuang, Jun Dong, Zhen‐Li Huang, Bing Shi
article en
1 citations

Abstract

Full automation of single-molecule localization microscopy (SMLM) is crucial for large-scale and high-throughput cellular imaging. It is well-known that SMLM typically consists of three major steps: immunofluorescence (IF) staining, optical imaging, and image processing. Currently, automation in optical imaging and image processing is almost complete; however, the automation of IF staining has been slow to advance, probably due to its complicated experimental operations. Here we present a low-cost automated method for IF staining, called super-resolution immunofluorescence staining by microfluidics (SRIF-fluidics). This method is suitable for both adherent and suspension cells and supports single-color and multi-color IF staining for SMLM. Our results show that SRIF-fluidics reduces antibody consumption by about 75% and shortens the sample preparation time from 5.6 hours (manual operation) to 2.5 ∼ 4.4 hours, depending on the sample types. Importantly, this method provides a satisfactory consistency of imaging results without sacrificing sample labeling quality. We believe that the method proposed in this paper is a necessary supplement to achieving fully automated SMLM and facilitating high-throughput SMLM in the near future.

Biomedical Optics ExpressVol. 15(12)
Hainan University (CN), Wuhan National Laboratory for Optoelectronics (CN), Huazhong University of Science and Technology (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 19%
Advanced Fluorescence Microscopy Techniques
0.66
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Microfluidics-based automatic immunofluorescence staining for single-molecule localization microscopy — Weibing Kuang, Jun Dong, et al. · Biomedical Optics Express (2024) | TGRS Research Map | TGRS