Abstract
Self-assembled monolayer (SAM) as a unique type of nanomaterials has played important roles in modern nanotechnology. In this study, we described a novel method to fabricate SAM with a surfactant-like peptide A6K, which has been known to self-assemble into micellar nanofibers in aqueous solution. Firstly a simple filtration method was used to remove self-assembling nanofibers and retain peptide monomers in solution. Pyrene-fluorescence, dynamic light scattering (DLS) and atomic force microscopy (AFM) were used to confirm that nanofibers were effectively removed and filtered solution contained only peptide monomers. Then by incubating the filtered peptide solution on mica surface, the peptide monomers could self-assemble into a flat and continuous peptide SAM, which was further proved to be a suitable substrate for creating nanopatterns by AFM nanolithography.
Keywords: Micelles, monomers, nanolithography, nanopatterns, self-assembled monolayer, self-assembling peptide.
Current Nanoscience
Title:Fabrication of Peptide Self-assembled Monolayer on Mica Surface and its Application in Atomic Force Microscopy Nanolithography
Volume: 10 Issue: 2
Author(s): Zhihua Xing, Yongzhu Chen, Chengkang Tang, Xiaoqiang Gong and Feng Qiu
Affiliation:
Keywords: Micelles, monomers, nanolithography, nanopatterns, self-assembled monolayer, self-assembling peptide.
Abstract: Self-assembled monolayer (SAM) as a unique type of nanomaterials has played important roles in modern nanotechnology. In this study, we described a novel method to fabricate SAM with a surfactant-like peptide A6K, which has been known to self-assemble into micellar nanofibers in aqueous solution. Firstly a simple filtration method was used to remove self-assembling nanofibers and retain peptide monomers in solution. Pyrene-fluorescence, dynamic light scattering (DLS) and atomic force microscopy (AFM) were used to confirm that nanofibers were effectively removed and filtered solution contained only peptide monomers. Then by incubating the filtered peptide solution on mica surface, the peptide monomers could self-assemble into a flat and continuous peptide SAM, which was further proved to be a suitable substrate for creating nanopatterns by AFM nanolithography.
Export Options
About this article
Cite this article as:
Xing Zhihua, Chen Yongzhu, Tang Chengkang, Gong Xiaoqiang and Qiu Feng, Fabrication of Peptide Self-assembled Monolayer on Mica Surface and its Application in Atomic Force Microscopy Nanolithography, Current Nanoscience 2014; 10 (2) . https://dx.doi.org/10.2174/15734137113096660111
DOI https://dx.doi.org/10.2174/15734137113096660111 |
Print ISSN 1573-4137 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6786 |
- Author Guidelines
- Graphical Abstracts
- Fabricating and Stating False Information
- Research Misconduct
- Post Publication Discussions and Corrections
- Publishing Ethics and Rectitude
- Increase Visibility of Your Article
- Archiving Policies
- Peer Review Workflow
- Order Your Article Before Print
- Promote Your Article
- Manuscript Transfer Facility
- Editorial Policies
- Allegations from Whistleblowers
Related Articles
-
Chagas Disease Chemotherapy: What Do We Know So Far?
Current Pharmaceutical Design The CXCL12/CXCR4 Axis as a Therapeutic Target in Cancer and HIV-1 Infection
Current Medicinal Chemistry Time Recall; Future Concept of Chronomodulating Chemotherapy for Cancer
Current Pharmaceutical Biotechnology Patent Selections
Recent Patents on Mechanical Engineering Ascorbic Acid in Cancer Chemoprevention: Translational Perspectives and Efficacy
Current Drug Targets Environmental Chemicals and Breast Cancer Risk – A Structural Chemistry Perspective
Current Medicinal Chemistry Radiolabelled Peptides: Eon in Radiopharmaceutical
Current Radiopharmaceuticals Tanshinone IIA: Pharmacology, Total Synthesis, and Progress in Structure-modifications
Current Medicinal Chemistry Advances in the Use of Stem Cells and Tissue Engineering Applications in Bone Repair
Current Stem Cell Research & Therapy Current Status Of Short Synthetic Peptides As Vaccines
Medicinal Chemistry Histopathological Determinants of Tumor Resistance: A Special Look to the Immunohistochemical Expression of Carbonic Anhydrase IX in Human Cancers
Current Medicinal Chemistry Targeting Cancer and Neuropathy with Histone Deacetylase Inhibitors:Two Birds with One Stone?
Current Cancer Drug Targets Epigallocatechin-3-gallate Increases RXRγ-mediated Pro-apoptotic and Anti-invasive Effects in Gastrointestinal Cancer Cell Lines
Current Cancer Drug Targets lGnRH-III - a Promising Candidate for Anticancer Drug Development
Protein & Peptide Letters Cellular Sensitivity to β-Diketonato Complexes of Ruthenium(III), Chromium(III) and Rhodium(III)
Medicinal Chemistry Low Doses Naltrexone: The Potential Benefit Effects for its Use in Patients with Cancer
Current Drug Research Reviews High-throughput Screening Identifies Small Molecule Inhibitors of Molecular Chaperones
Current Pharmaceutical Design Stable Expression of the Sodium/Iodide Symporter (NIS) for anti-Cancer Gene Therapy of Glioma Cells Using a Third Generation Self-Inactivating Lentiviral Vector System in Combination with 211At
Current Radiopharmaceuticals Advances in the Development of Class I Phosphoinositide 3-Kinase (PI3K) Inhibitors
Current Topics in Medicinal Chemistry Vitamin D and Vitamin D Analogs in Cancer Treatment
Current Drug Targets