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In Situ Caging of Biomolecules in Graphene Hybrids for Light Modulated Bioactivity.
Cheng, Gong; Han, Xiao-Hui; Hao, Si-Jie; Nisic, Merisa; Zheng, Si-Yang.
Afiliación
  • Cheng G; Department of Biomedical Engineering and ‡Material Research Institute, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.
  • Han XH; Department of Biomedical Engineering and ‡Material Research Institute, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.
  • Hao SJ; Department of Biomedical Engineering and ‡Material Research Institute, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.
  • Nisic M; Department of Biomedical Engineering and ‡Material Research Institute, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.
  • Zheng SY; Department of Biomedical Engineering and ‡Material Research Institute, The Pennsylvania State University , University Park, Pennsylvania 16802, United States.
ACS Appl Mater Interfaces ; 10(4): 3361-3371, 2018 Jan 31.
Article en En | MEDLINE | ID: mdl-29300454
Remote and noninvasive modulation of protein activity is essential for applications in biotechnology and medicine. Optical control has emerged as the most attractive approach owing to its high spatial and temporal resolutions; however, it is challenging to engineer light responsive proteins. In this work, a near-infrared (NIR) light-responsive graphene-silica-trypsin (GST) nanoreactor is developed for modulating the bioactivity of trypsin molecules. Biomolecules are spatially confined and protected in the rationally designed compartment architecture, which not only reduces the possible interference but also boosts the bioreaction efficiency. Upon NIR irradiation, the photothermal effect of the GST nanoreactor enables the ultrafast in situ heating for remote activation and tuning of the bioactivity. We apply the GST nanoreactor for remote and ultrafast proteolysis of proteins, which remarkably enhances the proteolysis efficiency and reduces the bioreaction time from the overnight of using free trypsin to seconds. We envision that this work not only provides a promising tool of ultrafast and remotely controllable proteolysis for in vivo proteomics in study of tissue microenvironment and other biomedical applications but also paves the way for exploring smart artificial nanoreactors in biomolecular modulation to gain insight in dynamic biological transformation.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Grafito Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Grafito Idioma: En Revista: ACS Appl Mater Interfaces Asunto de la revista: BIOTECNOLOGIA / ENGENHARIA BIOMEDICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos