Faculty Opinions recommendation of Scanning angle interference microscopy reveals cell dynamics at the nanoscale.

Author(s):  
Martin Gruebele ◽  
Max Platkov
2012 ◽  
Vol 9 (8) ◽  
pp. 825-827 ◽  
Author(s):  
Matthew J Paszek ◽  
Christopher C DuFort ◽  
Matthew G Rubashkin ◽  
Michael W Davidson ◽  
Kurt S Thorn ◽  
...  

Author(s):  
Cristina Bertocchi ◽  
Timothy J. Rudge ◽  
Andrea Ravasio

2016 ◽  
Vol 13 (11) ◽  
pp. 897-898 ◽  
Author(s):  
Catherine B Carbone ◽  
Ronald D Vale ◽  
Nico Stuurman

2019 ◽  
Author(s):  
Marshall J. Colville ◽  
Sangwoo Park ◽  
Warren R. Zipfel ◽  
Matthew J. Paszek

AbstractRecent advances in fluorescence microscopy have enabled the visualization of subcellular structures at unprecedented resolution. However, the complexity of state-of-the-art microscopes has increased considerably, often requiring the precise control and synchronization of multiple peripheral devices at high speeds. Drawing inspiration from open-source prototyping systems, like the Arduino, we describe the development of a new control platform that adopts the best features of these systems – affordability, facile programmability, and flexible connectivity – but with the scientific-grade inputs and outputs (I/O) and built-in routines that are necessary to control peripherals in advanced microscopy applications. Notably, our platform includes waveform generators and I/O for point-and azimuthal-scanning of excitation in laser-based applications. As a proof of concept, we show how the integration of waveform generation, multiplexed analog outputs, and native hardware triggers into a single central hub provides a versatile platform for performing fast circle-scanning acquisitions, including ring scanning-angle interference microscopy (SAIM), total internal reflection fluorescence (TIRF and ring TIRF) microscopy, and multiangle TIRF (MA-TIRF). We also demonstrate how the low communication latency of our hardware platform can reduce image intensity and reconstruction artifacts arising from synchronization errors produced by software control. Our complete platform, including hardware design files, firmware, API, software, and all associated source code, will be hosted for community-based development and collaboration.


2005 ◽  
Vol 94 (21) ◽  
Author(s):  
O. V. Sosnovtseva ◽  
A. N. Pavlov ◽  
N. A. Brazhe ◽  
A. R. Brazhe ◽  
L. A. Erokhova ◽  
...  

2016 ◽  
Author(s):  
Catherine B. Carbone ◽  
Ronald D. Vale ◽  
Nico Stuurman

AbstractWe describe open source software and hardware tools for calibrating, acquiring, and analyzing images for scanning angle interference microscopy (SAIM) analysis. These tools make it possible for any user with a TIRF microscope equipped with a motorized illumination unit to generate reconstructed images with nanometer precision in the axial (z) direction and diffraction-limited resolution in the lateral (xy) plane.


2009 ◽  
Vol 1 (1) ◽  
pp. 77-83 ◽  
Author(s):  
A. R. Brazhe ◽  
N. A. Brazhe ◽  
O. V. Sosnovtseva ◽  
A. N. Pavlov ◽  
E. Mosekilde ◽  
...  

Author(s):  
R. I. Johnsson-Hegyeli ◽  
A. F. Hegyeli ◽  
D. K. Landstrom ◽  
W. C. Lane

Last year we reported on the use of reflected light interference microscopy (RLIM) for the direct color photography of the surfaces of living normal and malignant cell cultures without the use of replicas, fixatives, or stains. The surface topography of living cells was found to follow underlying cellular structures such as nuceloli, nuclear membranes, and cytoplasmic organelles, making possible the study of their three-dimensional relationships in time. The technique makes possible the direct examination of cells grown on opaque as well as transparent surfaces. The successful in situ electron microprobe analysis of the elemental composition and distribution within single tissue culture cells was also reported.This paper deals with the parallel and combined use of scanning electron microscopy (SEM) and the two previous techniques in a study of living and fixed cancer cells. All three studies can be carried out consecutively on the same experimental specimens without disturbing the cells or their structural relationships to each other and the surface on which they are grown. KB carcinoma cells were grown on glass coverslips in closed Leighto tubes as previously described. The cultures were photographed alive by means of RLIM, then fixed with a fixative modified from Sabatini, et al (1963).


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