As recently published (Kellings
et al. J. gen Vir.
73, 1025-1029 (1992)), the analysis of purified scrapie prions by return refocusing gel electrophoresis revealed remaining nucleic acids in the size range up to 1100 nucleotides. The results defined the possible characteristics of a hypothetical scrapie-specific nucleic acid. If homogeneous in size, such a molecule would be less than 80 nucleotides in length at a particle-toinfectivity ratio (p: i) near unity; if heterogeneous, scrapie-specific nucleic acids would have to include molecules smaller than 240 nucleotides. To decrease the amount of nucleic acids, several modifications of the PrP
Sc
purification scheme were introduced. Instead of sucrose gradient, ultrafiltration was applied as a purification step and nucleic acids were degraded by BenzonasetM after ultrafiltration, but significant reduction of the p: i ratio could not be achieved. To prevent trapping of nucleic acids in prion rods, nuclease (Benzonase™ ) was added into the tissue homogenate and incubated at 37°C, overnight. The Benzonase treatment revealed no loss of infectivity, but the whole procedure of nucleic acid analysis did not lead to a reduction of the p :i ratio. In another approach the number of nucleic acid degradations steps was reduced to essentially two steps: Zn
2+
hydrolysis and Benzonase digestion. Higher Zn
2+
concentrations and prolonged incubation times resulted in a more efficient nucleic acid degradation. The bioassays yielded complete recovery of infectivity. Large-scale preparations for determining the p: i ratio are still underway
CRISPR/Cas12a Powered DNA Framework‐Supported Electrochemical Biosensing Platform for Ultrasensitive Nucleic Acid Analysis (Small Methods 12/2021)
