AI Article Synopsis

  • - Single-molecule localization microscopy (SMLM) is crucial for studying biological structures, but its long acquisition time can lead to drift artifacts.
  • - An innovative optical design using an electrically tunable lens (ETL) significantly reduces mechanical drift, achieving high precision in imaging (RMS ~0.7 nm lateral and ~2.7 nm axial).
  • - The ETL system allows for better imaging of transferrin receptors in B-lymphocytes, revealing distinct cluster patterns, and is also budget-friendly and compatible with current microscopy setups.

Article Abstract

Single-molecule localization microscopy (SMLM) has become an essential tool for examining a wide variety of biological structures and processes. However, the relatively long acquisition time makes SMLM prone to drift-induced artifacts. Here we report an optical design with an electrically tunable lens (ETL) that actively stabilizes a SMLM in three dimensions and nearly eliminates the mechanical drift (RMS ~0.7 nm lateral and ~2.7 nm axial). The bifocal design that employed fiducial markers on the coverslip was able to stabilize the sample regardless of the imaging depth. The effectiveness of the ETL was demonstrated by imaging endosomal transferrin receptors near the apical surface of B-lymphocytes at a depth of 8 µm. The drift-free images obtained with the stabilization system showed that the transferrin receptors were present in distinct but heterogeneous clusters with a bimodal size distribution. In contrast, the images obtained without the stabilization system showed a broader unimodal size distribution. Thus, this stabilization system enables a more accurate analysis of cluster topology. Additionally, this ETL-based stabilization system is cost-effective and can be integrated into existing microscopy systems.

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http://dx.doi.org/10.1364/OE.24.022959DOI Listing

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