用于低光剂量荧光激光扫描显微镜的冷却式SPAD阵列探测器。

IF 2.4 Q3 BIOPHYSICS
Eli Slenders, Eleonora Perego, Mauro Buttafava, Giorgio Tortarolo, Enrico Conca, Sabrina Zappone, Agnieszka Pierzynska-Mach, Federica Villa, Enrica Maria Petrini, Andrea Barberis, Alberto Tosi, Giuseppe Vicidomini
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引用次数: 0

摘要

异步读出单光子雪崩二极管(SPAD)阵列探测器的单光子时序和灵敏度性能以及成像能力为荧光(寿命)激光扫描显微镜(FLSM),如超分辨率图像扫描显微镜和高信息含量荧光波动光谱开辟了广阔的前景。然而,这些FLSM技术的优势取决于探测器的许多不同特性,如暗噪声、光子探测效率、后脉冲概率和光串扰,其整体优化通常是在这些特性之间的权衡。为了减轻这种权衡,据我们所知,我们提出了一种新型的SPAD阵列探测器,该探测器具有主动冷却系统,可以大大降低暗噪声,而不会显着恶化探测器的任何其他特性。特别是,我们表明,将传感器的温度降低到-15°C可以显着提高信噪比,因为与室温相比,暗计数率降低了10倍。因此,对于成像,激光功率可以降低三倍以上,这对活细胞超分辨率成像特别有益,正如在表达绿色荧光蛋白标记蛋白的固定细胞和活细胞中所证明的那样。对于荧光波动光谱,加上激光功率降低的好处,我们表明冷却探测器是必要的,以消除相关函数中的伪影,例如在探测器的热元素中观察到的虚假负相关,即暗噪声大大高于中位数的元素。总的来说,该探测器代表了在任何FLSM系统中集成SPAD阵列探测器的又一步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Cooled SPAD array detector for low light-dose fluorescence laser scanning microscopy.

Cooled SPAD array detector for low light-dose fluorescence laser scanning microscopy.

Cooled SPAD array detector for low light-dose fluorescence laser scanning microscopy.

Cooled SPAD array detector for low light-dose fluorescence laser scanning microscopy.

The single-photon timing and sensitivity performance and the imaging ability of asynchronous-readout single-photon avalanche diode (SPAD) array detectors have opened up enormous perspectives in fluorescence (lifetime) laser scanning microscopy (FLSM), such as super-resolution image scanning microscopy and high-information content fluorescence fluctuation spectroscopy. However, the strengths of these FLSM techniques depend on the many different characteristics of the detector, such as dark noise, photon-detection efficiency, after-pulsing probability, and optical cross talk, whose overall optimization is typically a trade-off between these characteristics. To mitigate this trade-off, we present, to our knowledge, a novel SPAD array detector with an active cooling system that substantially reduces the dark noise without significantly deteriorating any other detector characteristics. In particular, we show that lowering the temperature of the sensor to -15°C significantly improves the signal/noise ratio due to a 10-fold decrease in the dark count rate compared with room temperature. As a result, for imaging, the laser power can be decreased by more than a factor of three, which is particularly beneficial for live-cell super-resolution imaging, as demonstrated in fixed and living cells expressing green-fluorescent-protein-tagged proteins. For fluorescence fluctuation spectroscopy, together with the benefit of the reduced laser power, we show that cooling the detector is necessary to remove artifacts in the correlation function, such as spurious negative correlations observed in the hot elements of the detector, i.e., elements for which dark noise is substantially higher than the median value. Overall, this detector represents a further step toward the integration of SPAD array detectors in any FLSM system.

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来源期刊
Biophysical reports
Biophysical reports Biophysics
CiteScore
2.40
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审稿时长
75 days
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