Abstract

Three-dimensional RNA domain reconstruction is important for the assembly, disassembly and delivery functionalities of a packed proteinaceus capsid. However, to date, the self-association of RNA molecules is still an open problem. Recent chemical probing reports provide, with high reliability, the secondary structure of diverse RNA ensembles, such as those of viral genomes. Here, we present a method for reconstructing the complete 3D structure of RNA genomes, which combines a coarse-grained model with a subdomain composition scheme to obtain the entire genome inside proteinaceus capsids based on secondary structures from experimental techniques. Despite the amount of sampling involved in the folded and also unfolded RNA molecules, advanced microscope techniques can provide points of anchoring, which enhance our model to include interactions between capsid pentamers and RNA subdomains. To test our method, we tackle the satellite tobacco mosaic virus (STMV) genome, which has been widely studied by both experimental and computational communities. We provide not only a methodology to structurally analyze the tertiary conformations of the RNA genome inside capsids, but a flexible platform that allows the easy implementation of features/descriptors coming from both theoretical and experimental approaches.

Highlights

  • Non-enveloped ones convey a direct relationship between capsid proteins and RNA molecules, which was the genesis of several research routes on the assembly, disassembly and delivery functionalities of RNA inside proteinaceus capsids [1,2,3,4,5,6,7,8,9,10,11,12]

  • The three-dimensional in virio and in vitro models of the satellite tobacco mosaic virus (STMV) genome are shown in Figures 2 and 3

  • Our results show a structural 3D domain reconstruction of the RNA genome from viral secondary structures, and propose a way to control the quality of the model based on further microscopic information and/or modeling hypotheses

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Summary

Introduction

Several chemical probing tools [21,22,23,24,25,26] have tackled possible ways to measure/detect RNA secondary structures; nowadays, they offer (with a reasonable probability) very sophisticated schemes able to propose whole genomes packed inside virus capsids [27], cells [23], among other biological systems [20] Those results provide valuable information of the secondary structures, which shall be used as a starting point for further computational reconstruction of three-dimensional structures [19,28,29,30]

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