Kato Yuna, Iwata Shuichi, Nasu Yusuke, Obata Akiko, Nagata Kenji, Campbell Robert E, Mizuno Toshihisa
Department of Life Science and Applied Chemistry, Graduate School of Engineering, Nagoya Institute of Technology Gokiso-cho, Showa-ku Nagoya Aichi 466-8555 Japan
Department of Chemistry, School of Science, The University of Tokyo Bunkyo-ku Tokyo 113-0033 Japan.
RSC Adv. 2023 Oct 10;13(42):29584-29593. doi: 10.1039/d3ra06108f. eCollection 2023 Oct 4.
The development of a new materials platform capable of sustaining the functionality of proteinous sensor molecules over an extended period without being affected by biological contaminants in living systems, such as proteases, is highly demanded. In this study, our primary focus was on fabricating new core-shell fibremats using unique polymer materials, capable of functionalizing encapsulated sensor proteins while resisting the effects of proteases. The core-fibre parts of core-shell fibremats were made using a newly developed post-crosslinkable water-soluble copolymer, poly(2-hydroxypropyl methacrylamide)--poly(diacetone methacrylamide), and the bifunctional crosslinking agent, adipic dihydrazide, while the shell layer of the nanofibers was made of nylon 6. Upon encapsulating the lactate-sensor protein eLACCO1.1 at the core-fibre part, the fibremat exhibited a distinct concentration-dependent fluorescence response, with a dynamic range of fluorescence alteration exceeding 1000% over the lactate concentration range of 0 to 100 mM. The estimated dissociation constant from the titration data was comparable to that estimated in a buffer solution. The response remained stable even after 5 cycles and in the presence of proteases. These results indicates that our core-shell fibremat platform could serve as effective immobilizing substrates for various sensor proteins, facilitating continuous and quantitative monitoring of various low-molecular-weight metabolites and catabolites in a variety of biological samples.
迫切需要开发一种新型材料平台,该平台能够在较长时间内维持蛋白质传感器分子的功能,且不受生物系统中生物污染物(如蛋白酶)的影响。在本研究中,我们主要致力于使用独特的聚合物材料制造新型核壳纤维垫,这种材料能够使封装的传感器蛋白功能化,同时抵抗蛋白酶的作用。核壳纤维垫的核纤维部分采用新开发的可后交联水溶性共聚物聚(甲基丙烯酸2-羟丙酯)-聚(双丙酮甲基丙烯酰胺)和双功能交联剂己二酸二酰肼制成,而纳米纤维的壳层则由尼龙6制成。在核纤维部分封装乳酸传感器蛋白eLACCO1.1后,纤维垫表现出明显的浓度依赖性荧光响应,在0至100 mM的乳酸浓度范围内,荧光变化的动态范围超过1000%。从滴定数据估计的解离常数与在缓冲溶液中估计的解离常数相当。即使在5个循环后以及存在蛋白酶的情况下,响应仍保持稳定。这些结果表明,我们的核壳纤维垫平台可以作为各种传感器蛋白的有效固定基质,有助于对各种生物样品中的各种低分子量代谢物和分解代谢物进行连续和定量监测。