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仿生隐匿表面用于可逆化学和细胞机械响应基底

Biomimetic cryptic site surfaces for reversible chemo- and cyto-mechanoresponsive substrates.

机构信息

Institut de Sciences des Matériaux de Mulhouse, IS2M-LRC 7228 CNRS/Université de Haute-Alsace, 15, Rue Jean Starcky, 68057 Mulhouse Cedex, France.

出版信息

ACS Nano. 2013 Apr 23;7(4):3457-65. doi: 10.1021/nn400356p. Epub 2013 Apr 4.

DOI:10.1021/nn400356p
PMID:23530596
Abstract

Chemo-mechanotransduction, the way by which mechanical forces are transformed into chemical signals, plays a fundamental role in many biological processes. The first step of mechanotransduction often relies on exposure, under stretching, of cryptic sites buried in adhesion proteins. Likewise, here we report the first example of synthetic surfaces allowing for specific and fully reversible adhesion of proteins or cells promoted by mechanical action. Silicone sheets are first plasma treated and then functionalized by grafting sequentially under stretching poly(ethylene glycol) (PEG) chains and biotin or arginine-glycine-aspartic acid (RGD) peptides. At unstretched position, these ligands are not accessible for their receptors. Under a mechanical deformation, the surface becomes specifically interactive to streptavidin, biotin antibodies, or adherent for cells, the interactions both for proteins and cells being fully reversible by stretching/unstretching, revealing a reversible exposure process of the ligands. By varying the degree of stretching, the amount of interacting proteins can be varied continuously.

摘要

化学机械转导,即将机械力转化为化学信号的方式,在许多生物学过程中起着至关重要的作用。机械转导的第一步通常依赖于将埋藏在粘附蛋白中的隐藏部位暴露在拉伸下。同样,在这里我们报告了第一个通过机械作用促进蛋白质或细胞特异性和完全可逆附着的合成表面的例子。硅酮片首先进行等离子体处理,然后在拉伸下依次接枝聚乙二醇(PEG)链和生物素或精氨酸-甘氨酸-天冬氨酸(RGD)肽进行功能化。在未拉伸的位置,这些配体不可用于其受体。在机械变形下,表面对链霉亲和素、生物素抗体或细胞变得具有特异性相互作用,蛋白质和细胞的相互作用都可以通过拉伸/未拉伸完全可逆,揭示了配体的可逆暴露过程。通过改变拉伸程度,可以连续改变相互作用蛋白质的数量。

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