Generalizable Strategy for Engineering Protein Particles with pH-Triggered Disassembly and Recoverable Protein Functionality
Author(s) -
Tomoya Suma,
Jiwei Cui,
Markus Müllner,
Yi Ju,
Junling Guo,
Ming Hu,
Frank Caruso
Publication year - 2015
Publication title -
acs macro letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.966
H-Index - 92
ISSN - 2161-1653
DOI - 10.1021/mz5007443
Subject(s) - linker , nucleic acid , protein engineering , chemistry , drug delivery , cleavage (geology) , small molecule , combinatorial chemistry , biomolecule , biophysics , biochemistry , enzyme , materials science , organic chemistry , computer science , biology , fracture (geology) , composite material , operating system
Protein particles are promising candidates for therapeutic delivery. In this study, we report a generalizable strategy to assemble a series of proteins into pH-cleavable protein particles that recover protein functionality after disassembly. Our strategy uses an acid-labile reversible cross-linker based on maleic anhydride chemistry, which allows the cross-linking of proteins and releases unmodified proteins upon cleavage, causing minimal loss of protein functionality. The protein particles can be rapidly disassembled at a mildly acidic pH (<6.5) and inside cells with negligible cytotoxicity. Furthermore, cleavage of the cross-linker led to above 97% recovery of enzymatic activity, as evidenced by using glucose oxidase. This facile and robust strategy to engineer pH-cleavable protein particles may provide a new platform for therapeutic protein delivery as well as for small molecule drug and nucleic acid delivery.
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