Literature DB >> 17149935

High-resolution optical imaging from trajectory time distributions.

Erwen Mei1, Robin M Hochstrasser.   

Abstract

Trajectory time distribution optical microscopy (TTDOM), which records the mean off-times of single molecular fluorescent indicators that light up when they collide with vesicles, is extended to record fluorescence durations or on-times. TTDOM can distinguish shapes of objects that are smaller than the diffraction limited resolution. The fluorescence duration time image can also provide high-resolution information. The effects of the threshold that separates fluorescent bursts from background signals and of two or more probes visiting the vesicles simultaneously have been investigated systematically. New experimental results along with simulations indicate that TTDOM is capable of providing the size and shape of objects and information on probe-vesicle binding.

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Year:  2006        PMID: 17149935     DOI: 10.1021/jp065142f

Source DB:  PubMed          Journal:  J Phys Chem B        ISSN: 1520-5207            Impact factor:   2.991


  2 in total

Review 1.  Switchable Fluorophores for Single-Molecule Localization Microscopy.

Authors:  Honglin Li; Joshua C Vaughan
Journal:  Chem Rev       Date:  2018-09-17       Impact factor: 60.622

Review 2.  Transient Fluorescence Labeling: Low Affinity-High Benefits.

Authors:  Maxim M Perfilov; Alexey S Gavrikov; Konstantin A Lukyanov; Alexander S Mishin
Journal:  Int J Mol Sci       Date:  2021-10-30       Impact factor: 5.923

  2 in total

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