Genetically Engineered Protein Corona‐based Cascade Nanozymes for Enhanced Tumor Therapy. (9th October 2022)
- Record Type:
- Journal Article
- Title:
- Genetically Engineered Protein Corona‐based Cascade Nanozymes for Enhanced Tumor Therapy. (9th October 2022)
- Main Title:
- Genetically Engineered Protein Corona‐based Cascade Nanozymes for Enhanced Tumor Therapy
- Authors:
- Liu, Zhijun
Liu, Qiqi
Zhang, Haoqi
Zhang, Xiangyun
Wu, Jin
Sun, Zhiyuan
Zhu, Mingsheng
Hu, Xueyan
Qi, Tianyi
Kang, Helong
Chen, Rui
Huang, Xinglu
Zhuang, Jie - Abstract:
- Abstract: The emergence of nanomedicine has provided a promising strategy to greatly enhance the therapeutic efficacy of O2 ‐dependent photodynamic therapy (PDT). However, plasma‐derived protein corona and/or discontinuous O2 supply substantially limit their tumor delivery efficiency and therapeutic outcomes. Herein, protein corona cloaking‐based cascade nanozymes are developed using genetically engineered human ferritin heavy chain nanocages (FTn) as unique pre‐coated protein corona and cascade nanozymes as steady O2 suppliers. Specifically, FTn is coated onto mesoporous silica nanoparticles (MSNs) to form FTn‐based protein corona, providing active targeting of tumor cells by binding with its receptor. In situ synthesis of ultra‐small Au nanoparticles in MSNs, and biomimetic incorporation of Ru nanoclusters into FTn inner cavity showed glucose oxidase‐like activity and catalase‐like activity, respectively. The two nanozymes are incorporated into MSNs nanoplatform to induce cascade and circular catalytic reactions by consuming glucose and H2 O2 within the tumor microenvironment. Compared to MSNs alone, the FTn‐based protein corona is capable of efficiently diminishing plasma‐derived protein corona formation to prolong blood circulation time and improving in vitro tumor cell uptake and in vivo tumor accumulation, thereby providing significantly enhanced therapeutic benefits of PDT by combining with the continuously produced O2 of cascade nanozymes. Abstract : To improve tumorAbstract: The emergence of nanomedicine has provided a promising strategy to greatly enhance the therapeutic efficacy of O2 ‐dependent photodynamic therapy (PDT). However, plasma‐derived protein corona and/or discontinuous O2 supply substantially limit their tumor delivery efficiency and therapeutic outcomes. Herein, protein corona cloaking‐based cascade nanozymes are developed using genetically engineered human ferritin heavy chain nanocages (FTn) as unique pre‐coated protein corona and cascade nanozymes as steady O2 suppliers. Specifically, FTn is coated onto mesoporous silica nanoparticles (MSNs) to form FTn‐based protein corona, providing active targeting of tumor cells by binding with its receptor. In situ synthesis of ultra‐small Au nanoparticles in MSNs, and biomimetic incorporation of Ru nanoclusters into FTn inner cavity showed glucose oxidase‐like activity and catalase‐like activity, respectively. The two nanozymes are incorporated into MSNs nanoplatform to induce cascade and circular catalytic reactions by consuming glucose and H2 O2 within the tumor microenvironment. Compared to MSNs alone, the FTn‐based protein corona is capable of efficiently diminishing plasma‐derived protein corona formation to prolong blood circulation time and improving in vitro tumor cell uptake and in vivo tumor accumulation, thereby providing significantly enhanced therapeutic benefits of PDT by combining with the continuously produced O2 of cascade nanozymes. Abstract : To improve tumor delivery efficiency and therapeutic outcomes, the protein corona cloaking‐based cascade nanozymes are developed using genetically engineered protein nanocages as unique pre‐coated protein corona and cascade nanozymes as steady O2 suppliers. The study offers a synthetic biology nanosystem for tumor catalytic therapy by incorporation of genetic engineering biotechnology and in situ biomimetic nanotechnology. … (more)
- Is Part Of:
- Advanced functional materials. Volume 32:Number 51(2022)
- Journal:
- Advanced functional materials
- Issue:
- Volume 32:Number 51(2022)
- Issue Display:
- Volume 32, Issue 51 (2022)
- Year:
- 2022
- Volume:
- 32
- Issue:
- 51
- Issue Sort Value:
- 2022-0032-0051-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-10-09
- Subjects:
- enzymatic cascade reactions -- ferritin nanocages -- mesoporous silica nanoparticles -- nanozymes -- protein corona
Materials -- Periodicals
Chemical vapor deposition -- Periodicals
620.11 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1616-3028 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adfm.202208513 ↗
- Languages:
- English
- ISSNs:
- 1616-301X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.853900
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 24707.xml