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Multi-Step Assembly of an RNA-Liposome Nanoparticle Formulation Revealed by Real-Time, Single-Particle Quantitative Imaging.

作者信息

Chung Michael C, Mendez-Gomez Hector R, Soni Dhruvkumar, McGinley Reagan, Zacharia Alen, Ashbrook Jewel, Stover Brian, Grippin Adam J, Sayour Elias J, Guan Juan

机构信息

Division of Chemical Biology and Medicinal Chemistry, College of Pharmacy, University of Texas at Austin, Austin, TX, 78712, USA.

Department of Physics, University of Florida, Gainesville, FL, 32611, USA.

出版信息

Adv Sci (Weinh). 2025 Mar;12(12):e2414305. doi: 10.1002/advs.202414305. Epub 2025 Jan 31.


DOI:10.1002/advs.202414305
PMID:39887619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11948016/
Abstract

Self-assembly plays a critical role in nanoparticle-based applications. However, it remains challenging to monitor the self-assembly of multi-component nanomaterials at a single-particle level, in real-time, with high throughput, and in a model-independent manner. Here, multi-color fluorescence microscopy is applied to track the assembly of both liposomes and mRNA simultaneously in clinical mRNA-based cancer immunotherapy. Imaging reveals that the assembly occurs in discrete steps: initially, RNA adsorbs onto the liposomes; then, the RNA-coated liposomes cluster into heterogeneous structures ranging from sub-micrometer to tens of micrometers. The clustering process is consistent with a Smoluchowski model with a Brownian diffusion kernel. The transition between the two steps of assembly is determined by the orientation of RNA-mediated interactions. Given the facile application of this approach and the ubiquity of the components studied, the imaging and analysis in this work are readily applied to monitor multi-component assembly of diverse nanomaterials.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/d6ca4a2bcd86/ADVS-12-2414305-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/3d464369f695/ADVS-12-2414305-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/56a045becf14/ADVS-12-2414305-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/00240ad29cb5/ADVS-12-2414305-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/c3ba75a2bee6/ADVS-12-2414305-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/282456c37ef8/ADVS-12-2414305-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/9d1129909f70/ADVS-12-2414305-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/7ab9e0a5fa6d/ADVS-12-2414305-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/d6ca4a2bcd86/ADVS-12-2414305-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/3d464369f695/ADVS-12-2414305-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/56a045becf14/ADVS-12-2414305-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/00240ad29cb5/ADVS-12-2414305-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/c3ba75a2bee6/ADVS-12-2414305-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/282456c37ef8/ADVS-12-2414305-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/9d1129909f70/ADVS-12-2414305-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/7ab9e0a5fa6d/ADVS-12-2414305-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba11/11948016/d6ca4a2bcd86/ADVS-12-2414305-g003.jpg

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[1]
Multi-Step Assembly of an RNA-Liposome Nanoparticle Formulation Revealed by Real-Time, Single-Particle Quantitative Imaging.

Adv Sci (Weinh). 2025-3

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
RNA aggregates harness the danger response for potent cancer immunotherapy.

Cell. 2024-5-9

[2]
Supramolecular Assembly in Live Cells Mapped by Real-Time Phasor-Fluorescence Lifetime Imaging.

J Am Chem Soc. 2024-5-1

[3]
Elucidating Structural Configuration of Lipid Assemblies for mRNA Delivery Systems.

ACS Nano. 2024-4-30

[4]
Aqueous Circularly Polarized Luminescence Induced by Homopolypeptide Self-Assembly.

J Am Chem Soc. 2023-12-20

[5]
Enzyme-Instructed Peptide Assembly Favored by Preorganization for Cancer Cell Membrane Engineering.

J Am Chem Soc. 2023-3-1

[6]
Enabling Genetic Code Expansion and Peptide Macrocyclization in mRNA Display via a Promiscuous Orthogonal Aminoacyl-tRNA Synthetase.

J Am Chem Soc. 2023-1-25

[7]
mRNA nanomedicine: Design and recent applications.

Exploration (Beijing). 2022-9-19

[8]
Optimization of Lipid Nanoformulations for Effective mRNA Delivery.

Int J Nanomedicine. 2022

[9]
In Situ Real-Time Nanoscale Resolution of Structural Evolution and Dynamics of Fluorescent Self-Assemblies by Super-Resolution Imaging.

Angew Chem Int Ed Engl. 2022-8-22

[10]
Nanoparticle single-cell multiomic readouts reveal that cell heterogeneity influences lipid nanoparticle-mediated messenger RNA delivery.

Nat Nanotechnol. 2022-8

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