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Peptide valence-induced breaks in plasmonic coupling

Electrostatic interactions are a key driving force that mediates colloidal assembly. The Schulze-Hardy rule states that nanoparticles have a higher tendency to coagulate in the presence of counterions with high charge valence. However, it is unclear how the Schulze–Hardy rule works when the simple e...

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Detalles Bibliográficos
Autores principales: Chang, Yu-Ci, Jin, Zhicheng, Li, Ke, Zhou, Jiajing, Yim, Wonjun, Yeung, Justin, Cheng, Yong, Retout, Maurice, Creyer, Matthew N., Fajtová, Pavla, He, Tengyu, Chen, Xi, O’Donoghue, Anthony J., Jokerst, Jesse V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993903/
https://www.ncbi.nlm.nih.gov/pubmed/36908948
http://dx.doi.org/10.1039/d2sc05837e
Descripción
Sumario:Electrostatic interactions are a key driving force that mediates colloidal assembly. The Schulze-Hardy rule states that nanoparticles have a higher tendency to coagulate in the presence of counterions with high charge valence. However, it is unclear how the Schulze–Hardy rule works when the simple electrolytes are replaced with more sophisticated charge carriers. Here, we designed cationic peptides of varying valencies and demonstrate that their charge screening behaviors on anionic gold nanoparticles (AuNPs) follow the six-power relationship in the Schulze–Hardy rule. This finding further inspires a simple yet effective strategy for measuring SARS-CoV-2 main protease (M(pro)) via naked eyes. This work provides a unique avenue for fundamental NP disassembly based on the Schulze–Hardy rule and can help design versatile substrates for colorimetric sensing of other proteases.