显微镜
烟酰胺腺嘌呤二核苷酸
荧光
双光子激发显微术
荧光显微镜
二次谐波产生
荧光寿命成像显微镜
激发态
生物物理学
高次谐波产生
化学
材料科学
光学
生物
NAD+激酶
激光器
生物化学
物理
原子物理学
酶
作者
Warren R. Zipfel,Rebecca M. Williams,Richard H. Christie,Alexander Yu. Nikitin,Bradley T. Hyman,Watt W. Webb
标识
DOI:10.1073/pnas.0832308100
摘要
Multicolor nonlinear microscopy of living tissue using two- and three-photon-excited intrinsic fluorescence combined with second harmonic generation by supermolecular structures produces images with the resolution and detail of standard histology without the use of exogenous stains. Imaging of intrinsic indicators within tissue, such as nicotinamide adenine dinucleotide, retinol, indoleamines, and collagen provides crucial information for physiology and pathology. The efficient application of multiphoton microscopy to intrinsic imaging requires knowledge of the nonlinear optical properties of specific cell and tissue components. Here we compile and demonstrate applications involving a range of intrinsic molecules and molecular assemblies that enable direct visualization of tissue morphology, cell metabolism, and disease states such as Alzheimer's disease and cancer.
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