Targeted Tuning of Interactive Forces by Engineering of Molecular Bonds in Series and Parallel Using Peptide-Based Adhesives.
Targeted Tuning of Interactive Forces by Engineering of Molecular Bonds in Series and Parallel Using Peptide-Based Adhesives.
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通过使用肽基粘合剂对串联和并联分子键进行工程设计,有针对性地调节相互作用力
DOI:
10.1021/acs.langmuir.5b02746
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发表时间:
2015
期刊:
影响因子:
--
通讯作者:
Valtiner
中科院分区:
文献类型:
--
作者:
Valtiner
Polymer-mediated adhesion plays a major role for both technical glues and biological processes like self-assembly or biorecognition. In contrast to engineering systems, adhesive strength in biological systems is precisely tuned via well-adjusted arrangement of individual bonds. How adhesion may be engineered by arrangement of individual bonds is however not yet well-understood. Here we show how the number of bonds in series and parallel can significantly influence adhesion forces using specifically designed surface-bridging peptides. We directly measure how adhesion forces between −COOH and −NH2functionalized surfaces across aqueous media vary as a function of the number of bonds in parallel. We also introduce surface bridging peptide sequences that are similarly end-functionalized with amines and carboxylic acid. Compared to single molecular junctions, adhesive strength mediated by these surface bridging peptides decreases by a factor of 2 for adhesive junctions that consist of two acid/base bonds in series. Furthermore, adhesive strength varies with the density of bonds in parallel. For dense systems, we observe that the formation of a bridging peptide monolayer is sterically hindered and therefore adhesion is further reduced significantly by 20%. Our results unravel how the arrangement of individual bonds in an adhesive junction allows for a wide tuning of adhesive strength on the basis of utilizing just one single specific bond. As such, for peptide adhesives it is essential to consider bonds in parallel in a wide range of applications where both high adhesion and triggered release of adhesive bonds is essential.
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影响因子:
3.4
作者:
Evans, E;Ritchie, K
通讯作者:
Ritchie, K
影响因子:
3.4
作者:
LECKBAND, D;MULLER, W;RINGSDORF, H
通讯作者:
RINGSDORF, H
DOI:
--
发表时间:
1996
期刊:
Biotechnology progress (Print)
影响因子:
--
作者:
A. Saterbak;D. Lauffenburger
通讯作者:
D. Lauffenburger
影响因子:
16.6
作者:
Raman, Sangeetha;Utzig, Thomas;Valtiner, Markus
通讯作者:
Valtiner, Markus
影响因子:
3.9
作者:
Utzig, Thomas;Raman, Sangeetha;Valtiner, Markus
通讯作者:
Valtiner, Markus