Nature’s antifreeze: The smaller the better
U. LEEDS (UK) — Cryoprotectants—compounds that act as a natural antifreeze to protect drugs, food, and tissue—work best when small, according to new research.
The findings, published in the journal Proceedings of the National Academy of Sciences, could help scientists develop better storage techniques for a range of materials, including human reproductive tissue used in in vitro fertilization.
Biological systems can usually only operate within a small range of temperatures. If they get too hot or too cold, the molecules within the system can become damaged, which affects their structure and stops them from functioning.
But certain species of fish, reptiles, and amphibians can survive for months below freezing by entering into a kind of suspended animation. They’re able to survive extreme conditions thanks to osmolytes—small molecules within their blood that act like antifreeze—preventing damage to their vital organs.
Osmolytes are used widely in the storage and testing of drugs and other pharmaceuticals; in food production; and to store human tissue like egg and sperm cells at very low temperatures (below -40ºC) for a long period of time.
“If you put something like human tissue straight in the freezer, ice crystals start to grow in the freezing water and solutes, solid particles dissolved in the water, get forced out into the remaining liquid,” says Lorna Dougan of the University of Leeds.
“This can result in unwanted high concentrations of solutes, such as salt, which can be very damaging to the tissue. The addition of cryoprotectants, such as glycerol, lowers the freezing temperature of water and prevents crystallization by producing a ‘syrupy’ semi-solid state. The challenge is to know which cryoprotectant molecule to use and how much of it is necessary.
“We want to get this right so that we recover as much of the biological material as possible after re-thawing. This has massive cost implications, particularly for the pharmaceutical industry because at present they lose a large proportion of their viable drug every time they freeze it.”
Dougan tested a range of different osmolytes to find out which ones are most effective at protecting the 3-D structure of a protein and used an atomic force microscope to unravel a test protein in a range of different osmolyte environments to find out which ones were most protective.
Smaller molecules, such as glycerol, proved to be more effective than larger ones like sorbitol.
“We’ve been able to show that if you want to really stabilize a protein, it makes sense to use small protecting osmolytes. We hope to use this discovery and future research to develop a simple set of rules that will allow scientists and industry to use the best process parameters for their system and in doing so dramatically increase the amount of material they recover from the freeze-thaw cycle.”
The research was funded by the UK Engineering and Physical Sciences Research Council, the US National Institutes of Health and the China National Basic Research Program.
Researchers from the University of Illinois and Columbia University contributed to the study.
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