Koho Sami V, Slenders Eli, Tortarolo Giorgio, Castello Marco, Buttafava Mauro, Villa Federica, Tcarenkova Elena, Ameloot Marcel, Bianchini Paolo, Sheppard Colin J R, Diaspro Alberto, Tosi Alberto, Vicidomini Giuseppe
Molecular Microscopy and Spectroscopy, Istituto Italiano di Tecnologia, Genoa, Italy.
University of Turku, Department of Cell Biology and Anatomy, Institute of Biomedicine and Medicity Research Laboratories, Laboratory of Biophysics, Turku, Finland.
Biomed Opt Express. 2020 May 7;11(6):2905-2924. doi: 10.1364/BOE.374398. eCollection 2020 Jun 1.
Two-photon excitation (2PE) laser scanning microscopy is the imaging modality of choice when one desires to work with thick biological samples. However, its spatial resolution is poor, below confocal laser scanning microscopy. Here, we propose a straightforward implementation of 2PE image scanning microscopy (2PE-ISM) that, by leveraging our recently introduced single-photon avalanche diode (SPAD) array detector and a novel blind image reconstruction method, is shown to enhance the effective resolution, as well as the overall image quality of 2PE microscopy. With our adaptive pixel reassignment procedure ∼1.6 times resolution increase is maintained deep into thick semi-transparent samples. The integration of Fourier ring correlation based semi-blind deconvolution is shown to further enhance the effective resolution by a factor of ∼2 - and automatic background correction is shown to boost the image quality especially in noisy images. Most importantly, our 2PE-ISM implementation requires no calibration measurements or other input from the user, which is an important aspect in terms of day-to-day usability of the technique.
当人们希望处理厚生物样本时,双光子激发(2PE)激光扫描显微镜是首选的成像方式。然而,其空间分辨率较差,低于共聚焦激光扫描显微镜。在此,我们提出了一种2PE图像扫描显微镜(2PE-ISM)的直接实现方法,通过利用我们最近推出的单光子雪崩二极管(SPAD)阵列探测器和一种新颖的盲图像重建方法,该方法被证明可以提高2PE显微镜的有效分辨率以及整体图像质量。通过我们的自适应像素重新分配程序,在厚半透明样本的深处分辨率提高约1.6倍得以维持。基于傅里叶环相关的半盲去卷积的整合被证明可将有效分辨率进一步提高约2倍,并且自动背景校正被证明可提高图像质量,特别是在有噪声的图像中。最重要的是,我们的2PE-ISM实现不需要校准测量或用户的其他输入,这在该技术的日常可用性方面是一个重要方面。