扫描电镜
显微镜
光漂白
荧光显微镜
荧光寿命成像显微镜
分辨率(逻辑)
光学
超分辨显微术
荧光
材料科学
纳米技术
受激发射
物理
计算机科学
人工智能
激光器
作者
Niels Radmacher,Alexey I. Chizhik,Oleksii Nevskyi,José Ignacio Gallea,Ingo Gregor,Jörg Enderlein
标识
DOI:10.1146/annurev-biophys-071524-105321
摘要
Over the last 30 years, fluorescence microscopy, renowned for its sensitivity and specificity, has undergone a revolution in resolving ever-smaller details. This advancement began with stimulated emission depletion (STED) microscopy and progressed with techniques such as photoactivatable localization microscopy and stochastic optical reconstruction microscopy (STORM). Single-molecule localization microscopy (SMLM), which encompasses methods like direct STORM, has significantly enhanced image resolution. Even though its speed is slower than that of STED, SMLM achieves higher resolution by overcoming photobleaching limitations, particularly through DNA point accumulation for imaging in nanoscale topography (DNA-PAINT), which continuously renews fluorescent labels. Additionally, cryo-fluorescence microscopy and advanced techniques like minimal photon fluxes imaging (MINFLUX) have pushed the boundaries toward molecular resolution SMLM. This review discusses the latest developments in SMLM, highlighting methods like resolution enhancement by sequential imaging (RESI) and PAINT-MINFLUX and exploring axial localization techniques such as supercritical angle fluorescence and metal-induced energy transfer. These advancements promise to revolutionize fluorescence microscopy, providing resolution comparable to that of electron microscopy.
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