Modulating Protein Corona and Materials-Cell Interactions with Temperature-Responsive Materials

被引:25
作者
Prawatborisut, Mongkhol [1 ,2 ]
Jiang, Shuai [1 ,3 ,4 ]
Oberlander, Jennifer [3 ,5 ]
Mailander, Volker [3 ,5 ]
Crespy, Daniel [1 ,2 ]
Landfester, Katharina [3 ]
机构
[1] Vidyasirimedhi Inst Sci & Technol VISTEC, Max Planck VISTEC Partner Lab Sustainable Mat, Rayong 21210, Thailand
[2] Vidyasirimedhi Inst Sci & Technol VISTEC, Sch Mol Sci & Engn, Dept Mat Sci & Engn, Rayong 21210, Thailand
[3] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
[4] Ocean Univ China, Sch Med & Pharm, Key Lab Marine Drugs, Chinese Minist Educ, Qingdao 266003, Peoples R China
[5] Johannes Gutenberg Univ Mainz, Univ Med Johannes Gutenberg, Dermatol Clin, Langenbeckstr 1, D-55131 Mainz, Germany
关键词
cell uptake; materials-cell interactions; protein adsorption; protein corona; temperature-responsive; CULTURE SURFACE; THERMORESPONSIVE HYDROGELS; HEAT INACTIVATION; DRIVING FORCES; ADSORPTION; POLYMERS; PLASMA; NANOPARTICLES; DETACHMENT; ADHESION;
D O I
10.1002/adfm.202106353
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Temperature-responsive polymers display changes of conformation upon a certain threshold temperature, which involves changes of hydrophobicity. Therefore, this property can be exploited to construct materials showing temperature-dependent interactions with proteins and cells. Indeed, the amounts and types of proteins in the protein corona after incubating temperature-responsive materials in protein mixtures are regulated by the surface hydrophobicity of materials. This ability is beneficial for designing systems for protein separation or for protecting proteins from thermal stress. Temperature-responsive materials are also employed for controlling cell adhesion and detachment. The cells are incubated at physiological temperature of mammalians (37 degrees C) followed by desorption of cell sheets at lower temperature when the substrate is hydrophilic. The authors envision that temperature-responsive materials will be employed for controlling protein corona of nanocarriers for drug delivery applications.
引用
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页数:16
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