Data Entry: Please note that the research database will be replaced by UNIverse by the end of October 2023. Please enter your data into the system https://universe-intern.unibas.ch. Thanks

Login for users with Unibas email account...

Login for registered users without Unibas email account...

 
Shedding light on biology of bacterial cells
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 3624013
Author(s) Schneider, Johannes P.; Basler, Marek
Author(s) at UniBasel Basler, Marek
Schneider, Johannes
Year 2016
Title Shedding light on biology of bacterial cells
Journal Philosophical Transactions of the Royal Society of London, Series B : Biological Sciences
Volume 371
Number 1707
Pages / Article-Number 20150499
Abstract To understand basic principles of living organisms one has to know many different properties of all cellular components, their mutual interactions but also their amounts and spatial organization. Live-cell imaging is one possible approach to obtain such data. To get multiple snapshots of a cellular process, the imaging approach has to be gentle enough to not disrupt basic functions of the cell but also have high temporal and spatial resolution to detect and describe the changes. Light microscopy has become a method of choice and since its early development over 300 years ago revolutionized our understanding of living organisms. As most cellular components are indistinguishable from the rest of the cellular contents, the second revolution came from a discovery of specific labelling techniques, such as fusions to fluorescent proteins that allowed specific tracking of a component of interest. Currently, several different tags can be tracked independently and this allows us to simultaneously monitor the dynamics of several cellular components and from the correlation of their dynamics to infer their respective functions. It is, therefore, not surprising that live-cell fluorescence microscopy significantly advanced our understanding of basic cellular processes. Current cameras are fast enough to detect changes with millisecond time resolution and are sensitive enough to detect even a few photons per pixel. Together with constant improvement of properties of fluorescent tags, it is now possible to track single molecules in living cells over an extended period of time with a great temporal resolution. The parallel development of new illumination and detection techniques allowed breaking the diffraction barrier and thus further pushed the resolution limit of light microscopy. In this review, we would like to cover recent advances in live-cell imaging technology relevant to bacterial cells and provide a few examples of research that has been possible due to imaging.This article is part of the themed issue 'The new bacteriology'.
Publisher Royal Society of London
ISSN/ISBN 0080-4622 ; 1471-2970
edoc-URL http://edoc.unibas.ch/44318/
Full Text on edoc No
Digital Object Identifier DOI 10.1098/rstb.2015.0499
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/27672150
ISI-Number WOS:000385338300006
Document type (ISI) Journal Article, Review
 
   

MCSS v5.8 PRO. 0.458 sec, queries - 0.000 sec ©Universität Basel  |  Impressum   |    
03/05/2024