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采用中子反射率研究的丝层。

Silk layering as studied with neutron reflectivity.

机构信息

School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, United States.

出版信息

Langmuir. 2012 Aug 7;28(31):11481-9. doi: 10.1021/la300916e. Epub 2012 Jul 26.

DOI:10.1021/la300916e
PMID:22697306
Abstract

Neutron reflectivity (NR) measurements of ultrathin surface films (below 30 nm) composed of Bombyx mori silk fibroin protein in combination with atomic force microscopy and ellipsometry were used to reveal the internal structural organization in both dry and swollen states. Reconstituted aqueous silk solution deposited on a silicon substrate using the spin-assisted layer-by-layer (SA-LbL) technique resulted in a monolayer silk film composed of random nanofibrils with constant scattering length density (SLD). However, a vertically segregated ordering with two different regions has been observed in dry, thicker, seven-layer SA-LbL silk films. The vertical segregation of silk multilayer films indicates the presence of a different secondary structure of silk in direct contact with the silicon oxide surface (first 6 nm). The layered structure can be attributed to interfacial β-sheet crystallization and the formation of well-developed nanofibrillar nanoporous morphology for the initially deposited silk surface layers with the preservation of less dense, random coil secondary structure for the layers that follow. This segregated structure of solid silk films defines their complex nonuniform behavior in the D(2)O environment with thicker silk films undergoing delamination during swelling. For a silk monolayer with an initial thickness of 6 nm, we observed the increase in the effective thickness by 60% combined with surprising decrease in density. Considering the nanoporous morphology of the hydrophobic silk layer, we suggested that the apparent increase in its thickness in liquid environment is caused by the air nanobubble trapping phenomenon at the liquid-solid interface.

摘要

利用中子反射率(NR)测量技术,结合原子力显微镜和椭圆偏振术,对桑蚕丝素蛋白组成的超薄膜(厚度低于 30nm)进行了研究,揭示了其在干燥和溶胀状态下的内部结构组织。使用旋转辅助层层(SA-LbL)技术,将再水合的丝素水溶液沉积在硅基底上,得到了由随机纳米原纤维组成的单层丝素薄膜,其散射长度密度(SLD)保持不变。然而,在干燥的、较厚的、七层 SA-LbL 丝素薄膜中观察到了垂直分层的有序排列,存在两种不同的区域。丝素多层膜的垂直分层表明,与氧化硅表面(前 6nm)直接接触的丝素具有不同的二级结构。分层结构归因于界面β-片晶结晶以及最初沉积的丝素表面层形成了发达的纳米原纤维纳米多孔形态,而后续的层则保持了密度较低的无规卷曲二级结构。这种固态丝素膜的分层结构决定了它们在 D(2)O 环境中的复杂非均相行为,较厚的丝素膜在溶胀过程中会分层。对于初始厚度为 6nm 的丝素单层,我们观察到有效厚度增加了 60%,同时密度惊人地降低。考虑到疏水丝素层的纳米多孔形态,我们认为在液体环境中其厚度的明显增加是由液体-固界面处空气纳米气泡捕获现象引起的。

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