Recent progress of fluorescence lifetime imaging microscopy technology and its application

被引:14
|
作者
Liu Xiong-Bo [1 ]
Lin Dan-Ying [1 ]
Wu Qian-Qian [1 ]
Yan Wei [1 ]
Luo Teng [1 ]
Yang Zhi-Gang [1 ]
Qu Jun-Le [1 ]
机构
[1] Shenzhen Univ, Coll Optoelect Engn, Key Lab Optoelect Devices & Syst, Minist Educ & Guangdong Prov, Shenzhen 518060, Peoples R China
基金
中国国家自然科学基金;
关键词
fluorescence lifetime imaging microscopy; fast imaging; super-resolution imaging; biomedical application; RESONANCE ENERGY-TRANSFER; PROTEIN INTERACTIONS; PHASOR APPROACH; FLIM; FRET; NANOPARTICLES; ILLUMINATION; PROBE; TOOL;
D O I
10.7498/aps.67.20180320
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
In the past decade, fluorescence lifetime imaging microscopy (FLIM) has been widely used in biomedical research and other fields. As the fluorescence lifetime is unaffected by probe concentration, excitation intensity and photobleaching, the FLIM has the advantages of high specificity, high sensitivity and capability of quantitative measurement in monitoring microenvironment changes and reflecting the intermolecular interactions. Despite decades of technical development, the FLIM technology still faces some challenges in practical applications. For example, its resolution is still difficult to overcome the diffraction limit and the trade-off among imaging speed, image quality and lifetime accuracy needs to be considered. In recent years, a great advance in FLIM and its application has been made due to the rapid development of hardware and software and their integration with other optical technologies. In this review, we first introduce the principle and characteristics of FLIM technology based on time domain and frequency domain. We then summarize the latest progress of FLIM technology: 1) imaging speed enhancement based on hardware improvement such as optimized time-correlated single photon counting module, single photon avalanche diode array detector, and acoustooptic deflector scanner; 2) lifetime measurement accuracy improvement by the proposed algorithms such as maximum likelihood estimate, Bayesian analysis and compressed sensing; 3) imaging quality enhancement and spatial resolution improvement by integrating FLIM with other optical technologies such as adaptive optics for correcting the aberration generated in the optical path, special illumination for equipping wide-field FLIM with optical sectioning ability, and super-resolution techniques for exceeding the resolution limit. We then highlight some recent applications in biomedical studies such as signal transduction or plant cell growth, disease diagnosis and treatment in cancers, Alzheimer's disease and skin diseases, assessment for toxicity and treatment efficiency of nanomaterials developed in the past few years. Finally, we present a short discussion on the current challenges and provide an outlook of the future development of enhanced imaging performance for FLIM technology. We hope that our summary on the state-of-the-art FLIM, our commentary on future challenges, and some proposed avenues for further advances will contribute to the development of FLIM technology and its applications in relevant fields.
引用
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页数:14
相关论文
共 73 条
  • [1] Alam S R, 2017, P SPIE OSA, V10414
  • [2] Alam S. R., 2017, P SOC PHOTO-OPT INS, P10069
  • [3] Time-resolved fluorescence microscopy (FLIM) as an analytical tool in skin nanomedicine
    Alexiev, Ulrike
    Volz, Pierre
    Boreham, Alexander
    Brodwolf, Robert
    [J]. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2017, 116 : 111 - 124
  • [4] Auksorius E, 2017, THESIS
  • [5] Stimulated emission depletion microscopy with a supercontinuum source and fluorescence lifetime imaging
    Auksorius, Egidijus
    Boruah, Bosanta R.
    Dunsby, Christopher
    Lanigan, Peter M. P.
    Kennedy, Gordon
    Neil, Mark A. A.
    French, Paul M. W.
    [J]. OPTICS LETTERS, 2008, 33 (02) : 113 - 115
  • [6] Fluorescence lifetime imaging - techniques and applications
    Becker, W.
    [J]. JOURNAL OF MICROSCOPY, 2012, 247 (02) : 119 - 136
  • [7] Detection of nucleic acid-protein interactions in plant leaves using fluorescence lifetime imaging microscopy
    Camborde, Laurent
    Jauneau, Alain
    Briere, Christian
    Deslandes, Laurent
    Dumas, Bernard
    Gaulin, Elodie
    [J]. NATURE PROTOCOLS, 2017, 12 (09) : 1933 - 1950
  • [8] Novel photosensitizer-protein nanoparticles for Photodynamic therapy: Photophysical characterization and in vitro investigations
    Chen, Kuan
    Preuss, Annegret
    Hackbarth, Steffen
    Wacker, Matthias
    Langer, Klaus
    Roeder, Beate
    [J]. JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2009, 96 (01) : 66 - 74
  • [9] [陈明惠 Chen Minghui], 2014, [激光生物学报, Acta Laser Biology Sinica], V23, P207
  • [10] Fluorescence Self-Quenching from Reporter Dyes Informs on the Structural Properties of Amyloid Clusters Formed in Vitro and in Cells
    Chen, WeiYue
    Young, Laurence J.
    Lu, Meng
    Zaccone, Alessio
    Strohl, Florian
    Yu, Na
    Schierle, Gabriele S. Kaminski
    Kaminski, Clemens F.
    [J]. NANO LETTERS, 2017, 17 (01) : 143 - 149