Near-isotropic super-resolution microscopy with axial interference speckle illumination

Super-resolution microscopy has pushed the limits of biological imaging. However, achieving isotropic resolution across all spatial dimensions remains a challenge and often requires a complex and highly sensitive optical setup. Herein, we introduce axial interference speckle illumination-engineered structured illumination microscopy (AXIS-SIM), a minimal-modification approach that utilizes constructive interference from a simple back-reflecting mirror to enhance the axial resolution without additional phase control or complex beam shaping. AXIS-SIM provides superior optical sectioning and improves axial resolution beyond the typical axial resolution of conventional 3D-structured illumination microscopy (~300 nm), achieving lateral and axial resolutions of 108.5 and 140.1 nm, respectively. Furthermore, its robustness against alignment errors and sample-induced aberrations enables high-throughput 3D super-resolution imaging of diverse biological specimens. We demonstrate its potential by visualizing the 3D morphology of cell membranes, resolving the nanoscale distribution of lysosomes and microtubules and tracking lysosomal movements with enhanced axial clarity.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-10-20
DOI
https://doi.org/10.1038/s41467-025-64366-2
Citations
1
Primary Topic
Advanced Fluorescence Microscopy Techniques
Type
article
Field-Weighted Citation Impact
1.63
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Near-isotropic super-resolution microscopy with axial interference speckle illumination

Hajun Yoo, Kwanhwi Ko, Seongmin Im, Sukhyeon Ka et al.
1 citations
Nature Communications
Advanced Fluorescence Microscopy Techniques
1.63
article

Near-isotropic super-resolution microscopy with axial interference speckle illumination

Hajun Yoo, Kwanhwi Ko, Seongmin Im, Sukhyeon Ka, Donghyun Kim, Peng Xi, Hyunwoong Lee, Gwiyeong Moon
article en
1 citations

Abstract

Super-resolution microscopy has pushed the limits of biological imaging. However, achieving isotropic resolution across all spatial dimensions remains a challenge and often requires a complex and highly sensitive optical setup. Herein, we introduce axial interference speckle illumination-engineered structured illumination microscopy (AXIS-SIM), a minimal-modification approach that utilizes constructive interference from a simple back-reflecting mirror to enhance the axial resolution without additional phase control or complex beam shaping. AXIS-SIM provides superior optical sectioning and improves axial resolution beyond the typical axial resolution of conventional 3D-structured illumination microscopy (~300 nm), achieving lateral and axial resolutions of 108.5 and 140.1 nm, respectively. Furthermore, its robustness against alignment errors and sample-induced aberrations enables high-throughput 3D super-resolution imaging of diverse biological specimens. We demonstrate its potential by visualizing the 3D morphology of cell membranes, resolving the nanoscale distribution of lysosomes and microtubules and tracking lysosomal movements with enhanced axial clarity.

Nature CommunicationsVol. 16(1)
University of Illinois Urbana-Champaign (US), Chinese University of Hong Kong (HK), Yonsei University (KR), Peking University (CN), Samsung (South Korea) (KR), Korea Innotech (South Korea) (KR)
Openalex Percentile: Top 11%
Advanced Fluorescence Microscopy Techniques
1.63
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.