Reliable software is a prerequisite for successful operation of a modern wide field fluorescence microscope. When used for live cell imaging, acquisition speed is of particular interest. This is both because biological processes can be highly‐dynamic, and to avoid unnecessary photobleaching and phototoxicity of living samples. This article shows that besides the hardware (microscope) components themselves, the acquisition control software is an important influencing factor of speed performance. We tested and compared the speed performance of five different generic applications (Image‐Pro Plus, MetaMorph, Micro‐Manager, SlideBook, and Volocity) using typical experimental setups involving a single specific state‐of‐the‐art fluorescence microscope configuration. The test measurements included multichannel experiments, z‐stacking, burst acquisition, as well as combinations of these measurements with time‐lapse acquisitions. The measured data provided values for guiding the testing and analysis of other microscope systems with similar configurations. Despite the identical hardware settings, significant and surprisingly large speed differences were evident among the various software applications. Additionally, no application was identifiable as the fastest in all tests. Our work pinpoints the importance of the control software in determining a system's “real” maximal imaging speed. The study could serve as basis for further tests, eventually influencing the system selection criteria for speed‐sensitive applications. Microsc. Res. Tech., 2010. © 2010 Wiley‐Liss, Inc.
[1]
Robert M Zucker,et al.
Evaluation of confocal microscopy system performance.
,
2001,
Methods in molecular biology.
[2]
Clifford M. Babbey,et al.
Performance comparison between the high‐speed Yokogawa spinning disc confocal system and single‐point scanning confocal systems
,
2005,
Journal of microscopy.
[3]
Murray.
Evaluating the performance of fluorescence microscopes
,
1998,
Journal of microscopy.
[4]
J. Swedlow,et al.
Evaluating performance in three-dimensional fluorescence microscopy
,
2007,
Journal of microscopy.
[5]
Michael Liebling,et al.
Fast fluorescence microscopy for imaging the dynamics of embryonic development
,
2008,
HFSP journal.
[6]
Jason R Swedlow,et al.
Measuring tubulin content in Toxoplasma gondii: A comparison of laser-scanning confocal and wide-field fluorescence microscopy
,
2002,
Proceedings of the National Academy of Sciences of the United States of America.