Protein Nanogels with Temperature-Induced Reversible Structures and Redox Responsiveness

Zhang, Y (Zhang, Yue)^[ 1,2 ] ; Zhang, JM (Zhang, Jiamin)^[ 3 ] ; Xing, C (Xing, Cheng)^[ 3 ] ; Zhang, MM (Zhang, Mingming)^[ 4,5 ] ; Wang, LY (Wang, Lianyong)^[ 3 ] ; Zhao, HY (Zhao, Hanying)^[ 1,2 ]

ACS BIOMATERIALS SCIENCE & ENGINEERING, 2016, 2(12): 2266-2275

DOI: 10.1021/acsbiomaterials.6b00490

 WOS:000389789200016


Abstract

There are many natural examples of smart structures that are able to change conformations and functionalities responding to the external stimuli. The responsiveness is directly related to their unique structures. In the design of new materials, it is crucial to endow these materials with the capabilities to change structures and functionalities under the external stimuli. In this research, virus-mimicking protein nanogels with temperature-induced reversible structures and redox responsiveness are synthesized by cross-linking a thermally responsive polymer poly(di(ethylene glycol) methyl ether methacrylate-co-2-(2-pyridyldisulfide) ethyl methacrylate) with reduced bovine serum albumin (BSA) molecules through thiol-disulfide exchange reaction. The lower critical solution temperature (LCST) and sizes of the nanogels can be controlled by controlling the reaction conditions. The nanogels are able to change their structures responding to the temperature change. Below the LCST, BSA molecules are embedded inside the nanogels and protected by the polymer chains. Above the LCST, polymer chains collapse forming the cores, and BSA moves to the shells to stabilize the nanogels. The disulfide-cross-linked nanogels are dissociated in the presence of glutathione. In vitro cytotoxicity assays and cell uptake assays demonstrate that the nanogels show low toxicity toward 3T3, 293T, and MCF-7 cells and can be internalized into the MCF-7 cells. The nanogels will find applications in protein delivery.