P K a shifting in double-stranded RNA is highly dependent upon nearest neighbors and bulge positioning

Jennifer L. Wilcox, Philip C. Bevilacqua

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Shifting of pKa's in RNA is important for many biological processes; however, the driving forces responsible for shifting are not well understood. Herein, we determine how structural environments surrounding protonated bases affect pKa shifting in double-stranded RNA (dsRNA). Using 31P NMR, we determined the pKa of the adenine in an A+·C base pair in various sequence and structural environments. We found a significant dependence of pKa on the base pairing strength of nearest neighbors and the location of a nearby bulge. Increasing nearest neighbor base pairing strength shifted the pKa of the adenine in an A+·C base pair higher by an additional 1.6 pKa units, from 6.5 to 8.1, which is well above neutrality. The addition of a bulge two base pairs away from a protonated A+·C base pair shifted the pKa by only ∼0.5 units less than a perfectly base paired hairpin; however, positioning the bulge just one base pair away from the A+·C base pair prohibited formation of the protonated base pair as well as several flanking base pairs. Comparison of data collected at 25 C and 100 mM KCl to biological temperature and Mg2+ concentration revealed only slight pKa changes, suggesting that similar sequence contexts in biological systems have the potential to be protonated at biological pH. We present a general model to aid in the determination of the roles protonated bases may play in various dsRNA-mediated processes including ADAR editing, miRNA processing, programmed ribosomal frameshifting, and general acid-base catalysis in ribozymes.

Original languageEnglish (US)
Pages (from-to)7470-7476
Number of pages7
JournalBiochemistry
Volume52
Issue number42
DOIs
StatePublished - Oct 22 2013

All Science Journal Classification (ASJC) codes

  • Biochemistry

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