首页> 外文期刊>ACS Omega >Protein-Stabilizing Effect of Amphiphilic Block Copolymers with a Tertiary Sulfonium-Containing Zwitterionic Segment
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Protein-Stabilizing Effect of Amphiphilic Block Copolymers with a Tertiary Sulfonium-Containing Zwitterionic Segment

机译:两性含叔Z两性离子链段的嵌段共聚物的蛋白质稳定作用

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Tertiary sulfonium-containing zwitterionic block copolymers consisting of N-acryloyl-l-methionine methyl sulfonium salt (A-Met(S+)-OH) and n-butyl acrylate (BA) were newly synthesized to develop a novel protein stabilizer. The zwitterionic block copolymers were prepared by reversible addition–fragmentation chain-transfer (RAFT) polymerization of BA using a hydrophilic macro-chain-transfer agent (CTA) obtained from N-acryloyl-l-methionine (A-Met-OH) and subsequent postmodification. RAFT polymerization of A-Met-OH using poly(BA) macro-CTA, followed by postmodification, also afforded the target poly(A-Met(S+)-OH)-b-poly(BA). The block copolymers stabilized horseradish peroxidase (HRP) during storage at 37 °C for 5 days, and the protein-stabilizing effect was enhanced with increase in the A-Met(S+)-OH content. In particular, the block copolymer with ~85% A-Met(S+)-OH content showed a significant protein-stabilizing effect at a temperature (37 °C) higher than the room temperature, which is highly desirable for practical and industrial applications. The addition of sucrose into the block copolymer–protein solution led to a considerable increase in the HRP activity under the same conditions. Excellent alkaline phosphatase stabilization at 37 °C for 12 days was also achieved using the block copolymers. The zwitterionic block copolymers with the optimal hydrophilic/hydrophobic balance were found to serve as efficient protein-stabilizing agents, in comparison with the corresponding homopolymer and random copolymers. Dynamic light scattering, zeta potential, transmission electron microscopy, and circular dichroism measurements revealed that the zwitterionic block copolymer stabilizes an enzyme by wrapping with a slight change in the size, whereas the secondary and ordered structures of the enzyme are maintained.
机译:新合成了由N-丙烯酰基-1-甲硫氨酸甲基sulf盐(A-Met(S +)-OH)和丙烯酸正丁酯(BA)组成的含叔ionic两性离子嵌段共聚物,以开发新型蛋白质稳定剂。两性离子嵌段共聚物是通过使用可得自N-丙烯酰基-1-甲硫氨酸(A-Met-OH)的亲水性大链转移剂(CTA)和随后的BA的可逆加成-断裂链转移(RAFT)聚合反应制备的后修改。使用聚(BA)宏观CTA进行A-Met-OH的RAFT聚合,然后进行后改性,也得到了目标聚(A-Met(S +)-OH)-b-聚(BA)。该嵌段共聚物在37°C下储存5天期间稳定了辣根过氧化物酶(HRP),并且随着A-Met(S +)-OH含量的增加,蛋白质稳定作用得到增强。特别是,A-Met(S +)-OH含量约为85%的嵌段共聚物在高于室温的温度(37°C)下表现出显着的蛋白质稳定作用,这在实际和工业应用中是非常需要的。在相同条件下,将蔗糖添加到嵌段共聚物-蛋白质溶液中导致HRP活性显着提高。使用嵌段共聚物还可以在37°C下保持12天出色的碱性磷酸酶稳定性。与相应的均聚物和无规共聚物相比,发现具有最佳亲水/疏水平衡的两性离子嵌段共聚物可作为有效的蛋白质稳定剂。动态光散射,ζ电势,透射电子显微镜和圆二色性测量显示,两性离子嵌段共聚物通过包裹而尺寸略有变化而稳定了酶,而维持了酶的二级和有序结构。

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