© GEORGE RETSECK
By far the majority of human tissues available for research exist as formalin-fixed, paraffin-embedded (FFPE) specimens. Preserving tissues in this way maintains their structure and allows for thin slices to be prepared for histological analyses, among other things. It had been assumed, however, that this “ridiculously harsh” preservation technique was incompatible with protein studies, explains neuroscientist Stephen Ginsberg of New York University (NYU). “The thought was that the fixation irrevocably damaged the proteins.”
Indeed, the gold-standard tissue preparation for proteome analyses was thought to be snap-freezing,...
In their latest study, the researchers microdissected millimeter-scale patches of specific neuron populations from 8 µm-thick slices of FFPE brain tissue obtained from Alzheimer’s disease patients. They then extracted the proteins for analysis by mass spectrometry.
The researchers detected approximately 400 proteins from samples containing around 12,000 neurons. And most of those proteins were neuronal or Alzheimer’s disease–related, confirming the validity of the technique. “It’s not going to give you the entire proteome,” says Ginsberg, who was not part of the study, “but what it does is give you access to tissues that you didn’t have before. . . . It’s very utilitarian.” (Scientific Reports, 5:15456, 2015)
|PROTEIN EXTRACTION FROM. . .||STORAGE||AVAILABILITY||EASE OF HANDLING||NO. OF PROTEINS DETECTED|
|Snap-frozen tissue||A few years at -80°C||Limited||Tissue is delicate and requires careful handling.||Varies depending on the tissue type, but from a 1.5 mm2 neuronal sample, 303 proteins have been detected by mass spectrometry (J Neural Transm, 122:993-1005, 2015)|
Many years at room
|In this study, 400 proteins were detectable by mass spectrometry in a 1.5 mm2 section of neurons|