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Related Concept Videos

RNA-seq03:21

RNA-seq

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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
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Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
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Selective deuteration of an RNA:RNA complex for structural analysis using small-angle scattering.

Aldrex Munsayac1, Wellington C Leite2, Jesse B Hopkins3

  • 1Department of Chemistry, University of Michigan, Ann Arbor, MI, 48109, USA.

Biorxiv : the Preprint Server for Biology
|September 24, 2024
PubMed
Summary

This study introduces a novel scattering method to analyze RNA:RNA complex structures. The technique combines computational modeling with experimental data to reveal conformational changes in RNA assemblies.

Keywords:
HIV-1 dimerization initiation site (DIS)RNA structureRNA structure modelingRNA:RNA complexesintegrative structural biologyisotopic labelingsmall-angle X-ray scattering (SAXS)small-angle neutron scattering (SANS)

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Area of Science:

  • Structural Biology
  • Biophysics
  • Molecular Biology

Background:

  • Protein-free RNA:RNA complexes are crucial for biological processes but are structurally underrepresented.
  • Understanding RNA:RNA complex dynamics is essential for deciphering their functions.

Purpose of the Study:

  • To develop and demonstrate a joint small-angle X-ray and neutron scattering (SAXS/SANS) approach for interrogating RNA:RNA complex structures.
  • To validate and refine computational models like AlphaFold 3 using experimental scattering data.

Main Methods:

  • Utilized SAXS to determine solution structures of individual RNAs and their complexes.
  • Employed SANS with isotope labeling and contrast matching (CM) to probe selectively deuterated RNA:RNA complexes.
  • Integrated in silico modeling with experimental SAXS/SANS data.

Main Results:

  • Measured solution structures of free RNAs and the overall RNA:RNA complex using SAXS.
  • Demonstrated SANS with CM and isotope labeling to analyze bound RNA structures within complexes.
  • Showcased how experimental data can validate and improve AlphaFold 3 predictions for RNA:RNA complexes.

Conclusions:

  • The combined SAXS/SANS approach, alongside in silico modeling, effectively analyzes conformational changes in RNA:RNA complexes.
  • This integrated strategy enhances the understanding of RNA structure within functional assemblies.
  • The method provides a powerful tool for studying dynamic RNA structures in solution.