Document Detail

Nanoscale dynamics and protein adhesivity of alkylamine self-assembled monolayers on graphene.
MedLine Citation:
PMID:  23301836     Owner:  NLM     Status:  Publisher    
Atom-scale molecular dynamics computer simulations are used to probe the structure, dynamics and energetics of alkylamine self-assembled monolayer (SAM) films on graphene, and to model the formation of molecular bilayers and protein complexes on the films. Routes toward the development and exploitation of functionalized graphene structures are detailed here, and we show that the SAM architecture can be tailored for use in emerging applications, e.g., electrically stimulated nerve fiber growth via the targeted binding of specific cell surface peptide sequences on the functionalized graphene scaffold. The simulations quantify the changes in film physisorption on graphene and alkyl chain packing efficiency as the film surface is made more polar by changing the terminal groups from methyl (-CH3) to amine (-NH2) to hydroxyl (-OH) groups. The mode of molecule packing dictates the orientation and spacing between terminal groups at the surface of the SAM, which determines the way in which successive layers build up on the surface, whether via formation of bilayers of the molecule or the immobilization of other (macro)molecules, e.g., proteins, on the SAM. The simulations show formation of ordered, stable assemblies of monolayers and bilayers of decylamine-based molecules on graphene. These films can serve as protein adsorption platforms, with a hydrophobin protein showing strong and selective adsorption by binding via its hydrophobic patch to methyl-terminated films and binding to amine-terminated films using its more hydrophilic surface regions. Design rules obtained from modeling the atom-scale structure of the films and interfaces may provide inputs to experiments for rational design of assemblies in which the electronic, physicochemical and mechanical properties of the substrate, film and protein layer can be tuned to provide the desired functionality.
Shane O'Mahony; Colm O'Dwyer; Chris Nijhuis; James C Greer; Aidan J Quinn; Damien Thompson
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Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2013-1-9
Journal Detail:
Title:  Langmuir : the ACS journal of surfaces and colloids     Volume:  -     ISSN:  1520-5827     ISO Abbreviation:  Langmuir     Publication Date:  2013 Jan 
Date Detail:
Created Date:  2013-1-10     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9882736     Medline TA:  Langmuir     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

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