A robust and versatile method for production and purification of large-scale RNA samples for structural biology.

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Karlsson H, Baronti L, Petzold K

RNA 26 (8) 1023-1037 [2020-08-00; online 2020-04-30]

Recent findings in genome-wide transcriptomics revealed that RNAs are involved in almost every biological process, across all domains of life. The characterization of native RNAs of unknown function and structure is particularly challenging due to their typical low abundance in the cell and the inherent sensitivity toward ubiquitous RNA degrading enzymes. Therefore, robust in vitro synthesis and extensive work-up methods are often needed to obtain samples amenable for biochemical, biophysical, and structural studies. Here, we present a protocol that combines the most recent advances in T7 in vitro transcription methodology with reverse phase ion pairing and ion exchange HPLC purification of RNAs for the production of yield-optimized large-scale samples. The method is easy to follow, robust and suitable for users with little or no experience within the field of biochemistry or chromatography. The complete execution of this method, for example, for production of isotopically labeled NMR samples, can be performed in less than a week.

Protein Science Facility (PSF) [Service]

PubMed 32354720

DOI 10.1261/rna.075697.120

Crossref 10.1261/rna.075697.120

pmc: PMC7373988
pii: rna.075697.120
medline: 9509184