Directional translocation resistance of Zika xrRNA
A Suma and L Coronel and G Bussi and C Micheletti, NATURE COMMUNICATIONS, 11, 3749 (2020).
xrRNAs from flaviviruses survive in host cells because of their exceptional dichotomic response to the unfolding action of different enzymes. They can be unwound, and hence copied, by replicases, and yet can resist degradation by exonucleases. How the same stretch of xrRNA can encode such diverse responses is an open question. Here, by using atomistic models and translocation simulations, we uncover an elaborate and directional mechanism for how stress propagates when the two xrRNA ends, 5 and 3 ', are driven through a pore. Pulling the 3 ' end, as done by replicases, elicits a progressive unfolding; pulling the 5 ' end, as done by exonucleases, triggers a counterintuitive molecular tightening. Thus, in what appears to be a remarkable instance of intra-molecular tensegrity, the very pulling of the 5 ' end is what boosts resistance to translocation and consequently to degradation. The uncovered mechanistic principle might be co-opted to design molecular meta-materials. p id=Par Zika xrRNAs survive in host cells because they can be unwound and copied by replicases, but resist degradation by exonucleases. Here authors use atomistic models and simulations and uncover that pulling into a pore the xrRNA 3 ' end, as done by replicases, causes progressive unfolding; pulling the 5 ' end, as done by exonucleases, triggers molecular tightening.
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