Visualization of single molecules building a viral capsid protein lattice through stochastic pathways

Direct visualization of pathways followed by single molecules while they spontaneously self-assemble into supramolecular biological machines may provide fundamental knowledge to guide molecular therapeutics and the bottom-up design of nanomaterials and nanodevices. Here, high-speed atomic force micr...

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Detalles Bibliográficos
Autores: Valbuena Jiménez, Alejandro, Maity, Sourav, García Mateu, Mauricio, Roos, Wouter H.
Tipo de recurso: artículo
Fecha de publicación:2020
País:España
Institución:Universidad Autónoma de Madrid
Repositorio:Biblos-e Archivo. Repositorio Institucional de la UAM
Idioma:inglés
OAI Identifier:oai:repositorio.uam.es:10486/706310
Acceso en línea:http://hdl.handle.net/10486/706310
https://dx.doi.org/10.1021/acsnano.0c03207
Access Level:acceso abierto
Palabra clave:Nanomaterials
Virus
Capsid Protein
High-Speed Atomic Force Microscopy
Self-Assembly
Single-Molecule
Biología y Biomedicina / Biología
Descripción
Sumario:Direct visualization of pathways followed by single molecules while they spontaneously self-assemble into supramolecular biological machines may provide fundamental knowledge to guide molecular therapeutics and the bottom-up design of nanomaterials and nanodevices. Here, high-speed atomic force microscopy is used to visualize self-assembly of the bidimensional lattice of protein molecules that constitutes the framework of the mature human immunodeficiency virus capsid. By real-time imaging of the assembly reaction, individual transient intermediates and reaction pathways followed by single molecules could be revealed. As when assembling a jigsaw puzzle, the capsid protein lattice is randomly built. Lattice patches grow independently from separate nucleation events whereby individual molecules follow different paths. Protein subunits can be added individually, while others form oligomers before joining a lattice or are occasionally removed from the latter. Direct real-time imaging of supramolecular selfassembly has revealed a complex, chaotic process involving multiple routes followed by individual molecules that are inaccessible to bulk (averaging) techniques