Literature DB >> 23867337

High-resolution multiphoton cryomicroscopy.

Karsten König1, Aisada Uchugonova2, Hans Georg Breunig3.   

Abstract

An ultracompact high-resolution multiphoton cryomicroscope with a femtosecond near infrared fiber laser has been utilized to study the cellular autofluorescence during freezing and thawing of cells. Cooling resulted in an increase of the intracellular fluorescence intensity followed by morphological modifications at temperatures below -10 °C, depending on the application of the cryoprotectant DMSO and the cooling rate. Furthermore, fluorescence lifetime imaging revealed an increase of the mean lifetime with a decrease in temperature. Non-destructive, label-free optical biopsies of biomaterial in ice can be obtained with sub-20 mW mean powers.
Copyright © 2013 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Biobank; Cryomicroscope; Cryopreservation; FLIM; Freezing; Multiphoton imaging; Two-photon

Mesh:

Year:  2013        PMID: 23867337     DOI: 10.1016/j.ymeth.2013.07.006

Source DB:  PubMed          Journal:  Methods        ISSN: 1046-2023            Impact factor:   3.608


  3 in total

1.  Advanced Confocal Microscopy Techniques to Study Protein-protein Interactions and Kinetics at DNA Lesions.

Authors:  Soňa Legartová; Jana Suchánková; Jana Krejčí; Alena Kovaříková; Eva Bártová
Journal:  J Vis Exp       Date:  2017-11-12       Impact factor: 1.355

2.  Distinguishing signal from autofluorescence in cryogenic correlated light and electron microscopy of mammalian cells.

Authors:  Stephen D Carter; Shrawan K Mageswaran; Zachary J Farino; João I Mamede; Catherine M Oikonomou; Thomas J Hope; Zachary Freyberg; Grant J Jensen
Journal:  J Struct Biol       Date:  2017-10-25       Impact factor: 2.867

3.  Redox State of Cytochromes in Frozen Yeast Cells Probed by Resonance Raman Spectroscopy.

Authors:  Konstantin A Okotrub; Nikolay V Surovtsev
Journal:  Biophys J       Date:  2015-12-01       Impact factor: 4.033

  3 in total

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