Broadband backscattering confocal microscopy enables label-free 3D live cell nanoscale sensitive imaging

Fluorescence microscopy is a cornerstone of biological research. However, fluorescent labeling is challenging in live cells and is constrained by photobleaching and phototoxicity. Label-free methods allow cells to be studied in their native state, but most techniques have poor contrast, lack 3D capability, rely on complex optics, or fail to provide structural information. We present here broadband backscattering confocal microscopy (BBCM), which employs a broadband supercontinuum laser and collects backscattered light in a confocal geometry using a photomultiplier tube. Broadband illumination averages out size-dependent oscillations that confound monochromatic backscattering. This eliminates blind spots and intensity ambiguities, allowing all scatterers to be visible, with the signal increasing approximately linearly with scatterer size. BBCM is easy to retrofit to standard confocal microscopes, requires no specialized optics, and is straightforward for nonspecialists. It enables high-contrast, label-free 3D imaging of live cells with size sensitivity to subcellular structures without employing custom optics or complex data processing.

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Publication Details

Journal
Science Advances
Published
2026-09-16
DOI
https://doi.org/10.1126/sciadv.aei8554
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
0.00

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article

Broadband backscattering confocal microscopy enables label-free 3D live cell nanoscale sensitive imaging

Le Qiu, Lev T. Perelman, Yuri N. Zakharov, Rebecca T. Perelman et al.
Science Advances
Advanced Fluorescence Microscopy Techniques
article

Broadband backscattering confocal microscopy enables label-free 3D live cell nanoscale sensitive imaging

Le Qiu, Lev T. Perelman, Yuri N. Zakharov, Rebecca T. Perelman, Mark F. Coughlan, Paul Kumar Upputuri, Xuejun Zhang, Lei Zhang, Umar Khan
article en

Abstract

Fluorescence microscopy is a cornerstone of biological research. However, fluorescent labeling is challenging in live cells and is constrained by photobleaching and phototoxicity. Label-free methods allow cells to be studied in their native state, but most techniques have poor contrast, lack 3D capability, rely on complex optics, or fail to provide structural information. We present here broadband backscattering confocal microscopy (BBCM), which employs a broadband supercontinuum laser and collects backscattered light in a confocal geometry using a photomultiplier tube. Broadband illumination averages out size-dependent oscillations that confound monochromatic backscattering. This eliminates blind spots and intensity ambiguities, allowing all scatterers to be visible, with the signal increasing approximately linearly with scatterer size. BBCM is easy to retrofit to standard confocal microscopes, requires no specialized optics, and is straightforward for nonspecialists. It enables high-contrast, label-free 3D imaging of live cells with size sensitivity to subcellular structures without employing custom optics or complex data processing.

Science AdvancesVol. 12(38)
Beth Israel Deaconess Medical Center (US), Harvard Bioscience (United States) (US)
National Science Foundation, National Institutes of Health
Openalex Percentile: Top 13%
Advanced Fluorescence Microscopy Techniques
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