Probing Biological Molecule Orientation and Polymer Surface Structure at the Polymer/Solution Interface In Situ

Polymers are widely used for many applications ranging from biomedical materials, marine antifouling coatings, membranes for biomolecule separation, to substrates for enzyme molecules for biosensing. For such applications, it is important to understand molecular interactions between biological molec...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 36(2020), 26 vom: 07. Juli, Seite 7681-7690
1. Verfasser: Lin, Ting (VerfasserIn)
Weitere Verfasser: Guo, Wen, Guo, Ruiying, Chen, Zhan
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't
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520 |a Polymers are widely used for many applications ranging from biomedical materials, marine antifouling coatings, membranes for biomolecule separation, to substrates for enzyme molecules for biosensing. For such applications, it is important to understand molecular interactions between biological molecules and polymer materials in situ in real time. Such understanding provides vital knowledge to manipulate biological molecule-polymer interactions and to optimize polymer surface structures to improve polymer performance. In this research, sum frequency generation (SFG) vibrational spectroscopy was applied to study interactions between peptides (serving as models for biological molecules) and deuterated polystyrene (d8-PS, serving as a model for polymer materials). The peptide conformations/orientations and polymer surface phenyl orientation during the peptide-d8-PS interactions were determined using SFG. It was found that the π-π interaction between the aromatic amino acids on peptides and phenyl groups on d8-PS surface does not play a significant role. Instead, the peptide-d8-PS interactions are mediated by general hydrophobic interactions between the peptides and the polymer surface 
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650 4 |a Research Support, Non-U.S. Gov't 
700 1 |a Guo, Wen  |e verfasserin  |4 aut 
700 1 |a Guo, Ruiying  |e verfasserin  |4 aut 
700 1 |a Chen, Zhan  |e verfasserin  |4 aut 
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