3.7: X-ray Fluorescence (XRF)

1. Preparing the Silicon Nitride Windows

1. Use reverse tweezers to pick up a window (silicon nitride windows will shatter if dropped).
2. Place window onto a glass slide, flat side up.
3. Adhere small pieces of Scotch tape to the sides of the window, and use these to adhere the windows to the bottom of the culture dish.
4. Sterilize the windows in culture dishes with UV radiation. This can be accomplished with the auto-crosslink setting on a UV-crosslinking cabinet, followed by further UV irradiation under the UV lamp in the laminar flow hood for about 1 h.

2. Plating the Cells onto the Sterilized Silicon Nitride Windows

1. Hold the dish with it tilted at about a 45° angle.
2. Add media by pipetting towards the side of the dish and slowly relieve the tilt angle to coat the window with media.
3. Add cells to the culture dish, in the same manner, and incubate.
4. Observe the cells occasionally using a light microscope to determine when they are ready to use.

3. Fixation and Drying of Cells

1. In a laminar flow hood, remove the media by gentle aspiration while tilting the dish as described above.
2. Add PBS, pipetting towards the side of the dish while holding it at angle. Slowly relieve the tilt angle to coat the window with PBS.
3. Remove the PBS with gentle aspiration.
4. Pipetting towards the side of the dish, and holding it at an angle, add 4% PFA/PBS, pH 7 to cover the cells. Keep in this solution for 20 min at room temperature.
5. Remove the PFA/PBS mixture, and dispose as hazardous material.
6. Add PBS, pipetting as described above.
7. Repeat steps 3.5 and 3.6 twice.
8. Remove the PBS by gentle aspiration.
9. Add 20 mM PIPES, 200 mM sucrose, pH 7.
10. Remove the PIPES/sucrose by gentle aspiration.
11. Repeat steps 2.8 and 2.9 twice.
12. Quickly blot the edges and back indentation of the window with a Kimwipe, then set the window on a clean surface, such as a rubber grid mat, to dry.

4. X-Ray Fluorescence Imaging of Cells

1. Once the sample is dry, verify the presence of cells on the windows using a light microscope.
2. Use nail polish to secure the windows to an aluminum holder provided by the beamline.
3. Insert the aluminum holder into a kinematic mount, and then place it into position at the focal point of the optics in the X-ray microscope, and at an angle of about 45° to the incident X-ray beam, mounted to the sample nanopositioning stages.
4. Exit the X-ray microscope instrument area (usually a hutch made of lead walls), and open the shutter. Conduct the remaining steps remotely.
5. Using either a zone plate, or Kirkpatrick-Baez mirrors, focus the monochromatic X-ray beam (usually 10 keV in energy) down to a sub-micron spot size.
6. Using the nanopositioning sample stages, and viewing the position of the X-ray beam on the sample with a pre-calibrated downstream scintillator camera, determine the appropriate width and height of the raster scan in order to capture data of the sample.
7. With the wavelength-dispersive silicon drift detector at 90° to the incident beam, and about 3 mm or less from the sample, collect a test spectrum with a dwell time of 1–2 sec.
8. Viewing the test spectrum, choose an appropriate dwell time for the scan, to provide sufficient signal-to-noise for the elements of interest.
9. Choose an appropriate resolution for the scan, one which is not significantly smaller than the spot size of the beam on the sample, nor larger than the features of interest in the sample.
10. Program the scan into the scanning software, and collect the image.

X-ray fluorescence, or XRF, spectroscopy is a non-destructive analytical technique that is used to perform elemental analysis of samples at room temperature.

XRF can be applied to a wide range of samples, including biological, forensic, environmental, and even works of art. The samples can also take a variety of forms, such as powders, crystals, and liquids. In XRF, a sample is bombarded with a beam of X-rays causing it to emit secondary X-rays at a lower energy, which are called fluorescent radiation.

Though it is referred to as a fluorescence technique, XRF differs from traditional fluorescence microscopy in that it does not use lower energy visible light, or light-active molecules.

This video will introduce the basics of XRF, and demonstrate how to collect elemental maps of a biological sample.

When a photon of sufficient energy collides with an atom, the energy is absorbed, exciting one of the outer shell electrons. As the electron relaxes, it emits a secondary photon, typically of lower energy. This process is known as fluorescence. Unlike lower-energy photons, like those used in fluorescence microscopy, X-ray photons are energetic enough to completely expel tightly held electrons from an inner shell. An electron from a higher-energy shell will then fall into the vacancy. A photon proportional to the energy difference between the two shells is released. Each element emits a unique set of photons, or spectrum, that can be used to identify the element and determine the quantity present. This phenomenon is known as X-ray fluorescence.

Once an elemental spectrum has been collected, the signals of elements of interest can be isolated. Measurements can be taken at multiple locations across a sample, generating an image, one pixel at a time. This process is known as raster scanning. Images of all elements of interest can be subsequently generated. These elemental maps provide valuable information about the sample. With an understanding of XRF, you are now ready to prepare a biological cell sample to generate elemental maps.

To begin, first prepare and sterilize a silicon nitride window, which will hold the sample in place for the scan. Use care, as they are very fragile. Orient the window so that it is flat side up. Then place the window in a culture dish, and adhere it?to the dish using small pieces of adhesive tape.

Finally, sterilize the silicon nitride window with UV radiation for 1 hr.

Now that the window has been sterilized, the sample can be fixed to it. First, hold the culture dish at an angle and add media to the side of the dish. Slowly relieve the tilt to coat the window. Add cells to the dish in the same manner, and incubate.

Periodically observe the cells under a light microscope until they are ready to use.

In a laminar flow hood, gently aspirate the media from the dish.

Then, rinse the cells with phosphate buffered saline to remove excess media.

Aspirate the PBS, and fix the cells with paraformaldehyde. After 20 min, remove the mixture and dispose as hazardous waste.

Remove the window from the dish, and quickly blot the edges and back indentation of the window with a Kimwipe. Set the window on a clean surface to dry.

Once the sample is dry, verify the presence of cells on the window with a light microscope.

Using clear nail polish, secure the window to an aluminum holder.

Insert the sample holder into the instrument mount, then place the mount on the X-ray microscopes' positioning stage.

Position the sample window at the focal point of the X-ray microscope optics, with a 45-degree angle to the incident beam.

Exit the instrument area and conduct the remaining steps remotely to minimize X-ray exposure.

Open the shutter, and use optics to?focus the monochromatic X-ray beam down to a sub-micrometer spot size.

The position of the spot can be imaged with a pre-calibrated camera. Using the positioning stages, determine the appropriate width and height needed to raster over the sample.

Collect a test spectrum of the element of interest with a dwell time of 1 ? 2 seconds.

From the test spectrum, choose an appropriate scan time in order to provide a sufficient signal-to-noise ratio for the elements of interest.

Then, determine the resolution needed for the sample. The resolution should be smaller than the features of interest, but larger than the spot size. Finally, program the scan into the scanning software, and collect the image.

In this experiment, an elemental map of a cell was performed for several different elements. Many metals, such as copper, iron, and zinc are important nutrients in the cell, and were clearly identified within the cell.

By determining where each metal is found in the cell, valuable information can be elucidated about its normal cellular processes. In addition, metal-based diseases can be?understood.

X-ray fluorescence is used in a wide range of scientific fields. The non-destructive nature of XRF enables its use in the study of historical artifacts. Art historians utilize the technique to determine the pigments originally used in works of art. This can elucidate information about the work, such as the provenance, colors that have faded over time, and the authenticity. Forensic scientists also use XRF in crime scene investigation. When a gun is fired, the surrounding area is coated with gun shot residue. Gun shot residue contains gun powder, ignition primer, and metal from the casing and bullet. The information collected with XRF can identify the culprit and weapon used.

Another field of study that lends itself to X-ray fluorescence is paleontology. Here, elemental information is collected from a trilobite fossil, a marine arthropod that lived over 250 million years ago.

By characterizing the elemental composition of fossils, new information can be gained about long extinct life. Better-preserved samples can even provide the composition of soft tissues that have deteriorated long ago.

You've just watched JoVE's introduction to X-ray fluorescence. You should now understand the theory of X-ray spectroscopy and how to collect elemental information from a wide range of sources.

Thanks for watching!