石英晶体微天平
单层
化学
牛血清白蛋白
生物分子
背景(考古学)
吸附
相间
图层(电子)
化学工程
分子
蛋白质吸附
纳米技术
化学物理
材料科学
色谱法
有机化学
遗传学
生物化学
生物
工程类
古生物学
作者
Evan Angelo Quimada Mondarte,Elisa Margarita Mendoza Zamarripa,Ryongsok Chang,Fan Wang,S. N. Song,Hiroyuki Tahara,T. Hayashi
出处
期刊:Langmuir
[American Chemical Society]
日期:2022-01-14
卷期号:38 (4): 1324-1333
被引量:9
标识
DOI:10.1021/acs.langmuir.1c02312
摘要
We investigated a viscous protein layer formed on self-assembled monolayers (SAMs) in crowded biological environments. The results were obtained through force spectroscopic measurements using colloidal probes and substantiated by exhaustive analysis using a quartz crystal microbalance with an energy dissipation technique. A hydrophobic SAM of n-octanethiol (C8 SAM) in bovine serum albumin (BSA) solution is buried under an adlayer of denatured BSA molecules and an additional viscous interphase layer that is five times more viscous than the bulk solution. C8 SAMs in fetal bovine serum induced a formation of a thicker adsorbed protein layer but with no observable viscous interphase layer. These findings show that a fouling surface is essentially inaccessible to any approaching molecules and thus has a new biological and physical identity arising from its surrounding protein layers. In contrast, the SAMs composed of sulfobetaine-terminated alkanethiol proved to be sufficiently protein-resistant and bio-inert even under crowded conditions due to a protective barrier of its interfacial water, which has implications in the accurate targeting of artificial particles for drug delivery and similar applications by screening any non-specific interactions. Finally, our strategies provide a platform for the straightforward yet effectual in vitro characterization of diverse types of surfaces in the context of targeted interactions in crowded biological environments.
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