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Enzyme:Nanoparticle Bioconjugates with Two Sequential Enzymes: Stoichiometry and Activity of Malate Dehydrogenase and Citrate Synthase on Au Nanoparticles

机译:酶:具有两种顺序酶的纳米颗粒生物共轭物:金纳米颗粒上的化学计量和苹果酸脱氢酶和柠檬酸合酶的活性

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摘要

We report the synthesis and characterization of bioconjugates in which the enzymes malate dehydrogenase (MDH) and/or citrate synthase (CS) were adsorbed to 30 nm diameter Au nanoparticles. Enzyme:Au stoichiometry and kinetic parameters (specific activity, kcat, KM, and activity per particle) were determined for MDH:Au, CS:Au, and three types of dual-activity MDH/CS:Au bioconjugates. For single-activity bioconjugates (MDH:Au and CS:Au), the number of enzyme molecules adsorbed per particle was dependent upon the enzyme concentration in solution, with multilayers forming at high enzyme:Au solution ratios. The specific activity of adsorbed enzyme increased with increasing number adsorbed per particle for CS:Au, but was less sensitive to stoichiometry for MDH:Au. Dual activity bioconjugates were prepared in three ways: (1) by adsorption of MDH followed by CS, (2) by adsorption of CS followed by MDH, and (3) by coadsorption of both enzymes from the same solution. The resulting bioconjugates differed substantially in the number of enzyme molecules adsorbed per particle, the specific activity of the adsorbed enzymes, and also the enzymatic activity per particle. Bioconjugates formed by adding CS to the Au nanoparticles before MDH was added exhibited higher specific activities for both enzymes than those formed by adding the enzymes in the reverse order. These bioconjugates also had 3-fold higher per-particle sequential activity for conversion of malate to citrate, despite substantially fewer copies of both enzymes present.
机译:我们报告了生物缀合物的合成和表征,其中苹果酸脱氢酶(MDH)和/或柠檬酸合酶(CS)被吸附到直径为30 nm的金纳米颗粒上。确定了MDH:Au,CS:Au和三种双重活性MDH / CS:Au生物缀合物的酶:Au化学计量和动力学参数(比活性,kcat,KM和每个颗粒的活性)。对于单活性生物共轭物(MDH:Au和CS:Au),每个颗粒吸附的酶分子数量取决于溶液中的酶浓度,并以高的酶:Au溶液比例形成多层。吸附的酶的比活性随CS:Au的每个颗粒吸附数的增加而增加,但对MDH:Au的化学计量灵敏度较差。具有三种活性的生物活性共轭物可以通过三种方式制备:(1)吸附MDH,然后吸附CS;(2)吸附CS,然后吸附MDH;(3)两种酶从同一溶液中共吸附。所得的生物缀合物在每个颗粒上吸附的酶分子数量,所吸附的酶的比活性以及每个颗粒的酶促活性方面存在显着差异。在添加MDH之前,通过在Au纳米颗粒中添加CS形成的生物结合物,与通过反向添加酶形成的结合物相比,对两种酶均显示出更高的比活。这些生物共轭物还具有将苹果酸转化为柠檬酸盐的每颗粒更高的3倍顺序活性,尽管存在两种酶的拷贝少得多。

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