光漂白
显微镜
不透明度
光学
薄层荧光显微镜
显微镜
材料科学
非线性声学
非线性系统
物理
荧光
扫描共焦电子显微镜
量子力学
作者
Baptiste Heiles,Flora Nelissen,Dion Terwiel,Byung Min Park,Eleonora Munoz Ibarra,Agisilaos Matalliotakis,Rick Waasdorp,Tarannum Ara,Pierina Barturen-Larrea,Mengtong Duan,Mikhail G. Shapiro,Valeria Gazzola,David Maresca
标识
DOI:10.1101/2024.07.31.605825
摘要
Abstract Light-sheet fluorescence microscopy has revolutionized biology by visualizing dynamic cellular processes in three dimensions. However, light scattering in thick tissue and photobleaching of fluorescent reporters limit this method to studying thin or translucent specimens. Here we show that non-diffractive ultrasonic beams used in conjunction with a cross-amplitude modulation sequence and nonlinear acoustic reporters enable fast and volumetric imaging of targeted biological functions. We report volumetric imaging of tumor gene expression at the cm 3 scale using genetically encoded gas vesicles, and localization microscopy of currently uncharted cerebral capillary networks using intravascular microbubble contrast agents. Nonlinear sound-sheet microscopy provides a ∼64x acceleration in imaging speed, ∼35x increase in imaged volume and ∼4x increase in classical imaging resolution compared to the state-of-the-art in biomolecular ultrasound.
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