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小角X射线散射(SAXS)结合SAXS驱动的分子动力学用于多链RNA组装体的结构分析

Small-Angle X-ray Scattering (SAXS) Combined with SAXS-Driven Molecular Dynamics for Structural Analysis of Multistranded RNA Assemblies.

作者信息

Rolband Lewis A, Chopra Kriti, Danai Leyla, Beasock Damian, van Dam Hubertus J J, Krueger Joanna K, Byrnes James, Afonin Kirill A

机构信息

Nanoscale Science Program, Department of Chemistry, University of North Carolina Charlotte, Charlotte, North Carolina 28223, United States.

Computational Science Initiative, Brookhaven National Laboratory, Upton, New York 11973, United States.

出版信息

ACS Appl Mater Interfaces. 2024 Dec 11;16(49):67178-67191. doi: 10.1021/acsami.4c12397. Epub 2024 Nov 26.

DOI:10.1021/acsami.4c12397
PMID:39593218
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11637918/
Abstract

Nucleic acids (RNA and DNA) play crucial roles in all living organisms and find wide utility in clinical settings. The convergence of rationally designed nucleic acid multistranded assemblies with embedded therapeutic properties has led to the development of a platform based on nucleic acid nanoparticles (NANPs). NANPs incorporate various functional moieties to deliver their combinations to diseased cells in a highly controlled manner. Given that the structure and composition of NANPs can also influence their immunorecognition and biological activities, thorough verification of all designs is essential. We introduce an experimental pipeline for small-angle X-ray scattering (SAXS) to gather structural details about the solution-state NANPs assembled from up to 12 RNA strands. To the best of our knowledge, this study represents the largest multistranded RNA nanoassemblies characterized in this manner to date. We show that synchronized implementation of SAXS-driven molecular dynamics simulations reveals the diverse conformational landscape inhabited by these assemblies and provides insights into their immunorecognition. The developed strategy expands the capabilities of therapeutic nucleic acids and emerging nucleic acid nanotechnologies.

摘要

核酸(RNA和DNA)在所有生物中都起着至关重要的作用,并在临床环境中有广泛的应用。具有嵌入治疗特性的合理设计的核酸多链组装体的融合导致了基于核酸纳米颗粒(NANPs)的平台的发展。NANPs包含各种功能部分,以高度可控的方式将它们的组合递送至患病细胞。鉴于NANPs的结构和组成也会影响其免疫识别和生物活性,对所有设计进行彻底验证至关重要。我们引入了一种用于小角X射线散射(SAXS)的实验流程,以收集有关由多达12条RNA链组装而成的溶液状态NANPs的结构细节。据我们所知,这项研究代表了迄今为止以这种方式表征的最大的多链RNA纳米组装体。我们表明,SAXS驱动的分子动力学模拟的同步实施揭示了这些组装体所占据的多样构象景观,并为它们的免疫识别提供了见解。所开发的策略扩展了治疗性核酸和新兴核酸纳米技术的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/b2cafb225504/am4c12397_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/5ac32cf14f8a/am4c12397_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/aab364b5db4a/am4c12397_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/56dea7c5e852/am4c12397_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/82855e621618/am4c12397_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/b2cafb225504/am4c12397_0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/5ac32cf14f8a/am4c12397_0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/aab364b5db4a/am4c12397_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/56dea7c5e852/am4c12397_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/82855e621618/am4c12397_0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a296/11647755/b2cafb225504/am4c12397_0005.jpg

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