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Peptide valence-induced breaks in plasmonic coupling.
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.
Afiliação
  • Chang YC; Materials Science and Engineering Program, University of California San Diego La Jolla California 92093 USA jjokerst@ucsd.edu.
  • Jin Z; Department of NanoEngineering, University of California San Diego La Jolla California 92093 USA.
  • Li K; Institute of Materials Research and Engineering, Agency for Science, Technology and Research Singapore 138634 Singapore.
  • Zhou J; Department of NanoEngineering, University of California San Diego La Jolla California 92093 USA.
  • Yim W; Materials Science and Engineering Program, University of California San Diego La Jolla California 92093 USA jjokerst@ucsd.edu.
  • Yeung J; Department of Bioengineering, University of California San Diego La Jolla California 92093 USA.
  • Cheng Y; Department of NanoEngineering, University of California San Diego La Jolla California 92093 USA.
  • Retout M; Department of NanoEngineering, University of California San Diego La Jolla California 92093 USA.
  • Creyer MN; Department of NanoEngineering, University of California San Diego La Jolla California 92093 USA.
  • Fajtová P; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego La Jolla California 92093 USA.
  • He T; Materials Science and Engineering Program, University of California San Diego La Jolla California 92093 USA jjokerst@ucsd.edu.
  • Chen X; School of Materials Science and Engineering, Nanyang Technological University Singapore 639798 Singapore.
  • O'Donoghue AJ; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego La Jolla California 92093 USA.
  • Jokerst JV; Materials Science and Engineering Program, University of California San Diego La Jolla California 92093 USA jjokerst@ucsd.edu.
Chem Sci ; 14(10): 2659-2668, 2023 Mar 08.
Article em En | MEDLINE | ID: mdl-36908948
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 (Mpro) 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.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article