Coassembly of Lysozyme and Amphiphilic Biomolecules
Driven by Unimer-Aggregate Equilibrium
Tao, YY (Tao, Yuanyuan)[ 1 ] ; Ma, XT (Ma, Xiaoteng)[ 1 ] ; Cai, YQ (Cai, Yaqian)[ 1 ] ; Liu, L (Liu, Li)[ 1 ] ; Zhao, HY (Zhao, Hanying)[ 1 ]
JOURNAL OF
PHYSICAL CHEMISTRY B, 2018, 122(14): 3900-3907
DOI: 10.1021/acs.jpcb.8b01447
WOS:000430641900021
Abstract
Synthesis
and self-assembly of bioconjugates composed of proteins and synthetic molecules
have been widely studied because of the potential applications in medicine,
biotechnology, and nanotechnology. One of the challenging research studies in
this area is to develop organic solvent-free approaches to the synthesis and
self-assembly of amphiphilic bioconjugates. In this research, dialysis assisted
approach, a method based on unimer-aggregate equilibrium, was applied in the
coassembly of lysozyme and conjugate of cholesterol and glutathione (Ch-GSH).
In phosphate buffer solution, amphiphilic Ch-GSH conjugate self-assembles into
vesicles, and the vesicle solution is dialyzed against lysozyme solution.
Negatively charged Ch-GSH unimers produced in the unimer-vesicle exchange
equilibrium, diffuse across the dialysis membrane and have electrostatic
interaction with positively charged lysozyme, resulting in the formation of
Ch-GSH-lysozyme bioconjugate. Above a critical concentration, the
three-component bioconjugate molecules self-assemble into bioactive vesicles.