Two-photon single particle tracking in 3-D

被引:5
|
作者
So, PTC
Ragan, T
Gratton, E
Carerro, J
Voss, E
机构
关键词
SPT; two-photon; 3-D; microscopy; tracking; phagocytosis;
D O I
10.1117/12.274323
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Transport processes are important in biology and medicine. Examples include virus docking and infection, endocytosis of extracellular protein and phagtocytosis of antigenic material. Trafficking driven by molecular motors inside a complex three dimensional environment is a shared common theme. The complex sequence of these events are difficult to resolve with conventional techniques where the action of many cells are asynchronously averaged. Single particle tracking (SPT) was developed by Ghosh and Webb to address this problem and has proven to be a powerful technique in understanding membrane-protein interaction. Since the traditional SPT method uses wide field illumination and area detectors, it is limited to the study of two-dimensional systems. In this presentation we report the development of a 3-D single particle tracking technique using two-photon excitation. Using a real-time feedback system, we can dynamically position the sub-femtoliter two-photon excitation volume to follow the fluorescent particle under transport by maximizing the detected fluorescent intensity. Further, fluorescence spectroscopy can be performed in real time along the particle trajectory to monitor the underlying biochemical signals driving this transport process. The first application of this instrument will focus on the study of antigen endocytosis process of macrophages.
引用
收藏
页码:45 / 56
页数:4
相关论文
共 50 条
  • [31] 3D Orbital Tracking in a Modified Two-photon Microscope: An Application to the Tracking of Intracellular Vesicles
    Anzalone, Andrea
    Annibale, Paolo
    Gratton, Enrico
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2014, (92):
  • [32] Compressive sensing for fast 3-D and random-access two-photon microscopy
    Wen, Chenyang
    Ren, Mindan
    Feng, Fu
    Chen, Wang
    Chen, Shih-Chi
    OPTICS LETTERS, 2019, 44 (17) : 4343 - 4346
  • [33] 3D real-time single particle tracking using two-photon fluorescence from bright dye-based organic nanoparticles
    Emperauger, Marie-Charlotte
    Kurek, Eleonore
    Semmer, Florian
    Perronet, Karen
    Daniel, Jonathan
    Blanchard-Desce, Mireille
    Marquier, Francois
    NANOSCALE, 2025, 17 (04) : 2304 - 2311
  • [34] Fast 3-D Imaging of Brain Organoids With a New Single-Objective Planar-Illumination Two-Photon Microscope
    Rakotoson, Irina
    Delhomme, Brigitte
    Djian, Philippe
    Deeg, Andreas
    Brunstein, Maia
    Seebacher, Christian
    Uhl, Rainer
    Ricard, Clement
    Oheim, Martin
    FRONTIERS IN NEUROANATOMY, 2019, 13
  • [35] Efficient two-photon absorbing photosensitizers based on diazafluorene moiety for 3-D TPP fabrication
    Yang, Byeong Il
    Kim, Ran Hee
    Lee, Kwang-Sup
    Yong, Son
    Lim, Tale Woo
    Yang, Dong-Yol
    MOLECULAR CRYSTALS AND LIQUID CRYSTALS, 2008, 486 : 1054 - 1062
  • [36] From fundamentals of two-photon processes to cellular mechanism of chemotherapy, to 3-D memory.
    Prasad, PN
    Schally, A
    Liebow, C
    Nagy, AA
    Pudavar, H
    Wang, X
    Krebs, LJ
    Sviatkewicz, J
    Reinhardt, BA
    Chong, C
    Kim, KS
    Lin, TC
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1999, 218 : U488 - U488
  • [37] Automated 3-D Detection of Dendritic Spines from In Vivo Two-Photon Image Stacks
    Singh, P. K.
    Hernandez-Herrera, P.
    Labate, D.
    Papadakis, M.
    NEUROINFORMATICS, 2017, 15 (04) : 303 - 319
  • [38] Automated 3-D Detection of Dendritic Spines from In Vivo Two-Photon Image Stacks
    P. K. Singh
    P. Hernandez-Herrera
    D. Labate
    M. Papadakis
    Neuroinformatics, 2017, 15 : 303 - 319
  • [39] Creating defined 3-D defects inside an opaline Ormocerg® matrix with two-photon lithography
    Lange, Birger
    Jhaveri, Shalin J.
    Steidl, Lorenz
    Ayothi, Ramakrishnan
    Ober, Christopher K.
    Zentel, Rudolf
    MACROMOLECULAR RAPID COMMUNICATIONS, 2007, 28 (08) : 922 - 926
  • [40] Confocal microscopy - Two-photon 3-D images give 100-nm resolution
    Marx, BR
    LASER FOCUS WORLD, 1998, 34 (05): : 52 - +