English

Depth-enhanced molecular imaging with two-photon oblique plane microscopy

Optics 2025-12-05 v2 Biological Physics Instrumentation and Detectors

Abstract

High-numerical-aperture (NA) oblique plane microscopy enables noninvasive fluorescence imaging of subcellular dynamics without requiring radical sample modification. However, performance degrades at depth in multicellular specimens as scattering and refractive-index heterogeneity raise out-of-focus background. We report a two-photon oblique plane microscope that improves resolution at depth by combining high-NA single-objective detection with multiphoton plane illumination. The microscope achieves  ⁣300\sim\!300 nm lateral and  ⁣650\sim\!650 nm axial resolution, with single-molecule sensitivity in vivo. Compared with two-photon point scanning, the lower illumination NA delivers an order of magnitude lower peak intensity, enabling > ⁣5×>\!5\times faster volumetric acquisition (up to 3.25×1063.25 \times 10^6 voxels s1^{-1}) with reduced photodamage. In multicellular contexts, near-infrared nonlinear excitation enhances contrast throughout the illumination depth by  ⁣2×\sim\!2\times and restores volumetric resolving power by > ⁣2×>\!2\times relative to linear excitation. We demonstrate these capabilities through molecular imaging of epithelial tissue, stem-cell-derived gastruloids, and living fruit fly embryos, including multicolor transcription-factor dynamics, optogenetic subcellular control, and single-mRNA tracking, all using standard glass-based mounting.

Keywords

Cite

@article{arxiv.2511.09462,
  title  = {Depth-enhanced molecular imaging with two-photon oblique plane microscopy},
  author = {Kevin Keomanee-Dizon and Yaakov Clenman and Alejandra Duran and Sergey Ryabichko and Pauline Hansen and Tohn Borjigin and Richard Thornton and Jared E. Toettcher and Harold M. McNamara},
  journal= {arXiv preprint arXiv:2511.09462},
  year   = {2025}
}

Comments

13 pages, 6 figures; supplementary material included

R2 v1 2026-07-01T07:34:11.264Z