Block-Copolymer Vesicles as Nanoreactors for Enzymatic Reactions

被引:95
作者
Chen, Qi [1 ]
Schoenherr, Holger [1 ]
Vancso, G. Julius [1 ]
机构
[1] Univ Twente, MESA Inst Nanotechnol, Dept Mat Sci & Technol Polymers, NL-7500 AE Enschede, Netherlands
关键词
block copolymers; enzymes; fluorogenic substrates; kinetics; MULTIPLE MORPHOLOGIES; CHEMICAL-REACTIONS; EXPONENTIAL DECAY; ENERGY-TRANSFER; SINGLE; KINETICS; FLUORESCENCE;
D O I
10.1002/smll.200801455
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The impact of the spatial confinement of polystyrene-block-poly (acrylic acid) (PS-b-PAA) block copolymer (BCP) vesicles on the reactivity of encapsulated bovine pancreas trypsin is studied. Enzymes, as well as small molecules, are encapsulated with loading efficiencies up to 30% in BCP vesicles with variable internal volumes between 0.014 aL (internal vesicle diameter, d(in) = 30 nm) and 8 aL (d(in) = 250 nm), obtained by manipulating the vesicle preparation conditions. The kinetics of the trypsin-catalyzed reaction of a fluorogenic substrate inside and outside the vesicles is quantitatively estimated using fluorescence spectroscopic analyses in conjunction with the use of NaNO2 as selective quencher for non-encapsulated fluorophores. The values of the catalytic turnover number obtained for reactions in differently sized nanoscale reactors show a significant increase (up to approximate to 5x) with decreasing BCP vesicle volume, while the values of the Michaelis-Menten constant decrease. The observed increase in enzyme efficiency by two orders of magnitude compared to bulk solution is attributed to an enhanced rate of enzyme-substrate and molecule-wall collisions inside the nanosized reactors, as predicted in the literature on the basis of Monte Carlo simulations.
引用
收藏
页码:1436 / 1445
页数:10
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