Don't have access to a fancy Airyscan or STED?
Do have access to a good ole fashion confocal?
You can still do super resolution imaging!🧵#microscopy
All you need are good microscopy and digital imaging fundamentals. Everything you need to know can be found here: ibiology.org/online-biology… /2
Digital images are made up of spatially defined boxes called 'pixels'. Images are collections of pixels assigned color shades from a lookup table. /3
Here is a very simple image represented by one of four possible shade values. The simple pattern in the image arises from the distribution of pixels in space. /4
Here's a more typical image. Mitochondria stained with TMRM dye. 8-bit depth, allowing 256 possible shade values. Two different lookup tables are presented. /5
A convolution operation systematically uses the neighboring pixel values to modify all the pixel values in an image. This can be used to smooth or sharpen images digitally. /6
Images from a confocal are actually representations of diffraction patterns. Each sub resolution point source of light interferes with its neighbors. /7
If you know the blur pattern of each point source, you can use a fourier transform to correct for the interference. This is known as deconvolution. /8
You'll need to measure the blur pattern (point spread function or PSF) using sub-resolution fluorescent beads. These can be obtained commercially for pretty cheap. The PSF can be calculated from images using MetroloJ plugin in ImageJ. /9
With the PSF in hand, deconvolution can be performed in imageJ using the Deconvolutionlab2 plugin. Here I used the Richardson-Lucy algorithm. The documentation explains all the available algorithms. /10
Here's a close-up of the improvement in signal to noise ratio for a zoomed in portion of the previous images. /12
Here's the final improvement from the original image. /13
Finally, you can push the resolution limit even more by restricting the diameter of the confocal pinhole aperture. This is very nicely explained in this paper👇 Happy imaging!! /14 sciencedirect.com/science/articl…
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We've been asked recently to share our method for making our @cricut vinyl microfluidics chambers. So yesterday we took some pictures🤓 Hope y'all find this helpful! 🧵1/n #CellBiology #microscopy cc' @Chris_W_Ward
@cricut is a bladed printer that can cut custom vinyl spacers. The spacers are ~90 um thick. Cut tolerance is about .093". 2/n
Interested in drugs and mitochondria? I recently had the opportunity to write a review article on the subject for #BioSciRep @PPPublishing
Check out the 🧵 for more about what I learned! 1/n
Mitochondria vary in structure and function among source tissues. Altering mitochondrial function results in complex phenotypic outcomes. /2
In vitro, xenobiotic effects on the mitochondrial energy transduction system can be described via a few qualitative models that help classify common types of interactions. /3