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Fabrication of biofunctional nanomaterials via Escherichia coli OmpF protein air/water interface insertion/integration with copolymeric amphiphiles

机译:通过大肠杆菌OmpF蛋白质空气/水界面插入/与共聚两亲物整合来制备生物功能纳米材料

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Fabrication of next-generation biologically active materials will involve the integration of proteins with synthetic membrane materials toward a wide spectrum of applications in nanoscale medicine, including high-throughput drug testing,energy conversion for powering medical devices,and bio- cloaking films for mimicry of cellular membrane surfaces toward the enhancement of implant biocompatibility.We have used ABA triblock copolymer membranes (PMOXA-PDMS-PMOXA) of varied thicknesses as platform materials for Langmuir film-based functionalization with the OmpF pore protein from Escherichia coli by fabricating monolayers of copolymer amphiphile-protein complexes on the air/water interface.Here we demonstrate that the ability for protein insertion at the air/water interface during device fabrication is dependent upon the initial surface coverage with the copolymer as well as copolymer thickness.Methacrylate-terminated block copolymer structures that were 4 nm (4METH) and 8 nm (8METH) in length were used as the protein reconstitution matrix, whereas a l-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) lipid (approx 4 nm thickness) was used as a comparison to demonstrate the effects of copolymer length on protein integration capabilities.Wilhemy surface pressure measurements (mN/m) revealed a greater protein insertion in the 4METH and POPC structures compared with the 8METH structure,indicating that shorter copolymer chains possess enhanced biomimicry of natural lipid-based membranes.In addition, comparisons between the isothermal characteristics of the 4METH,8METH,and POPC membranes reveal that phase transitions of the 4METH resemble a blend of the 8METH and POPC materials, indicating that the 4METH chain may possess hybrid properties of both copolymers and lipids. Furthermore,we have shown that following the deposition of the amphiphilic materials on the air/ water interface,the OmpF can be deposited directly on top of the amphiphiles (surface addition), thus effectively further enhancing protein insertion because of the buoying effects of the membranes. These characteristics of Langmuir-Blodgett-based fabrication of copolymer-biomolecule hybrids represent a synthesis strategy for next-generation biomedical materials.
机译:下一代生物活性材料的制造将涉及蛋白质与合成膜材料的集成,从而在纳米级医学中广泛应用,包括高通量药物测试,为医疗设备供电的能量转换以及用于仿制药的生物隐身膜。细胞膜表面,以提高植入物的生物相容性。我们已使用不同厚度的ABA三嵌段共聚物膜(PMOXA-PDMS-PMOXA)作为平台材料,通过制造共聚物两亲性单层膜,利用大肠杆菌的OmpF孔蛋白对Langmuir膜进行功能化。空气/水界面上的蛋白质复合物这里我们证明了在器件制造过程中蛋白质在空气/水界面上的插入能力取决于共聚物的初始表面覆盖率以及共聚物的厚度。甲基丙烯酸酯封端的嵌段共聚物结构在l中分别为4 nm(4METH)和8 nm(8METH)蛋白质被用作蛋白质重构基质,而l-棕榈酰基-2-油酰基-sn-甘油-3-磷酸胆碱(POPC)脂质(约4 nm厚)被用作比较,以证明共聚物长度对蛋白质的影响与8METH结构相比,Wilhemy表面压力测量结果(mN / m)显示4METH和POPC结构中的蛋白质插入更大,这表明较短的共聚物链具有天然脂质基膜的增强的仿生性。 4METH,8METH和POPC膜的等温特性表明,4METH的相变类似于8METH和POPC材料的混合物,表明4METH链可能同时具有共聚物和脂质的杂化特性。此外,我们已经表明,两亲性材料在空气/水界面上的沉积之后,OmpF可以直接沉积在两亲性材料的顶部(表面添加),从而由于膜的浮力效应而有效地进一步增强了蛋白质插入。共聚物-生物分子杂化物的基于Langmuir-Blodgett的制造方法的这些特征代表了下一代生物医学材料的合成策略。

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