UV Imaging of Crystallisation Experiments
- UV imaging occurs on every 5th inspection, coloured red below
- Sitting drop plates are imaged on days 0 (same day as setup), 1, 3, 5, 7, 10, 14, 21, 28, 35, 42, 49, 56, 63, 70
- LCP plates are imaged on days 0 (same day as setup), 1, 2, 3, 4, 5, 9, 13, 16, 20, 24, 27
About UV Imaging
Most proteins contain tryptophan, which when excited by UV light will fluoresce at between 300-350nm (it is solvatochromic). Given that protein crystals are concentrated areas of protein, they should glow brightly when illuminated with UV light. The UV imaging thus allows one to locate protein crystals easily, and to validate that you’ve grown a protein crystal and not a misleading salt crystal.
Obvious visual and UV imaging of protein crystals
‘Invisible’ protein crystals found using UV
Salt crystals and some localized precipitation
Of course there are caveats to the UV imaging:
- If the protein has no tryptophan residues, the UV fluorescence will be minimal.
- Most – but not all – salts do not fluoresce when illuminated UV light, so just because you see a crystal in a UV image does not guarantee that it is a protein crystal.
- Heavy protein precipitate will also fluoresce, for the same reason that crystals glow brightly – it is a concentrated region of the protein.
- Protein can concentrate at an air/liquid interface
- Some cofactors (haem, for example) appear to quench the UV fluorescence, and some of the chemicals used to crystallise proteins also attenuate the UV fluorescence – we have seen this with MPD, amongst other chemicals.
Look at the visible time course of your droplet as well as at the UV inspections to really interpret what you see. Protein can precipitate at any air/liquid interface, and bubbles created during robotic setup are no exception. Over time, the bubbles shrink, but the shadow of the bubbles can be seen in a ghost of protein skin that remains. This crumpled skin can fluoresce and glow just like crystals.
Insulin crystals which will not fluoresce in UV light
The images highlighted in green contain nitrates which quench UV fluorescence
Reference: Desbois, S.; Seabrook, S. A.; Newman, J., Some practical guidelines for UV imaging in the protein crystallization laboratory. Acta Crystallographica Section F 2013, 69 (2).