16-Ch Time-resolved Single-Molecule Spectroscopy Using Line Excitation

被引:0
|
作者
Ingargiola, Antonino [1 ]
Peronio, Pietro [2 ]
Lerner, Eitan [1 ]
Gulinatti, Angelo [2 ]
Rech, Ivan [2 ]
Ghioni, Massimo [2 ]
Weiss, Shimon [1 ]
Michalet, Xavier [1 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, 405 Hilgard Ave, Los Angeles, CA 90024 USA
[2] Politecn Milan, DEIB, Milan, Italy
来源
SINGLE MOLECULE SPECTROSCOPY AND SUPERRESOLUTION IMAGING X | 2017年 / 10071卷
关键词
single-molecule; fluorescence; high-throughput; TCSPC; SPAD array; ALTERNATING-LASER EXCITATION; FLUORESCENCE SPECTROSCOPY; SIMPLEX-METHOD; DYNAMICS; FRET;
D O I
10.1117/12.2256367
中图分类号
TH742 [显微镜];
学科分类号
摘要
Single-molecule spectroscopy on freely-diffusing molecules allows detecting conformational changes of biomolecules without perturbation from surface immobilization. Resolving fluorescence lifetimes increases the sensitivity in detecting conformational changes and overcomes artifacts common in intensity-based measurements. Common to all freely-diffusing techniques, however, are the long acquisition times. We report a time-resolved multispot system employing a 16-channel SPAD array and TCSPC electronics, which overcomes the throughput issue. Excitation is obtained by shaping a 532 nm pulsed laser into a line, matching the linear SPAD array geometry. We show that the line-excitation is a robust and cost-effective approach to implement multispot systems based on linear detector arrays.
引用
收藏
页数:12
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