Mark Tingey, Andrew Ruba, Samuel L Junod, Coby Rush, Jason Saredy, William E Brew, Weidong Yang
{"title":"Paired-objectives photon enhancement (POPE) microscopy: enhanced photon collection for fluorescence imaging.","authors":"Mark Tingey, Andrew Ruba, Samuel L Junod, Coby Rush, Jason Saredy, William E Brew, Weidong Yang","doi":"10.1038/s44172-025-00491-6","DOIUrl":null,"url":null,"abstract":"<p><p>Fluorescence microscopy is indispensable for visualizing biological structures and dynamics, yet its efficiency is limited-over half of emitted photons fall outside the objective's numerical aperture and go undetected. Here, we introduce Paired-Objectives Photon Enhancement (POPE) microscopy, which increases photon collection efficiency by up to two-fold using a single excitation source, single detector, and dual objectives. By integrating a 4f optical system with a reflective mirror positioned opposite the objective in an inverted microscope, POPE redirects a substantial portion of otherwise lost photons into the detection pathway. Compatible with super-resolution, confocal, epifluorescence, and autofluorescence modalities, POPE improves spatial resolution, acquisition speed, and signal-to-noise ratio, particularly under photon-limited conditions. It has been validated across fluorophore solutions, subcellular structures, live cells, and thick tissues, consistently enhancing imaging performance. As a modular and cost-effective upgrade for standard inverted microscopes, POPE extends access to high-sensitivity fluorescence imaging and enables new applications in cell biology, biophysics, and biomedical research.</p>","PeriodicalId":72644,"journal":{"name":"Communications engineering","volume":"4 1","pages":"159"},"PeriodicalIF":0.0000,"publicationDate":"2025-08-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12391377/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Communications engineering","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s44172-025-00491-6","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Fluorescence microscopy is indispensable for visualizing biological structures and dynamics, yet its efficiency is limited-over half of emitted photons fall outside the objective's numerical aperture and go undetected. Here, we introduce Paired-Objectives Photon Enhancement (POPE) microscopy, which increases photon collection efficiency by up to two-fold using a single excitation source, single detector, and dual objectives. By integrating a 4f optical system with a reflective mirror positioned opposite the objective in an inverted microscope, POPE redirects a substantial portion of otherwise lost photons into the detection pathway. Compatible with super-resolution, confocal, epifluorescence, and autofluorescence modalities, POPE improves spatial resolution, acquisition speed, and signal-to-noise ratio, particularly under photon-limited conditions. It has been validated across fluorophore solutions, subcellular structures, live cells, and thick tissues, consistently enhancing imaging performance. As a modular and cost-effective upgrade for standard inverted microscopes, POPE extends access to high-sensitivity fluorescence imaging and enables new applications in cell biology, biophysics, and biomedical research.