California Institute of Technology, Beckman Institute, Pasadena, CA,
Nat Methods. 2011 Jul 17;8(9):757-60. doi: 10.1038/nmeth.1652.
We implemented two-photon scanned light-sheet microscopy, combining nonlinear excitation with orthogonal illumination of light-sheet microscopy, and showed its excellent performance for in vivo, cellular-resolution, three-dimensional imaging of large biological samples. Live imaging of fruit fly and zebrafish embryos confirmed that the technique can be used to image up to twice deeper than with one-photon light-sheet microscopy and more than ten times faster than with point-scanning two-photon microscopy without compromising normal biology.
我们实现了双光子扫描光片显微镜,将非线性激发与光片显微镜的正交照明相结合,并展示了其在大生物样品的体内、细胞分辨率、三维成像方面的优异性能。对果蝇和斑马鱼胚胎的活体成像证实,该技术可以用于成像的深度比单光子光片显微镜深一倍以上,速度比点扫描双光子显微镜快十倍以上,而不会影响正常生物学。