Abstract

The morphological and mechanical properties of thiolated ssDNA films self-assembled at different ionic strength on flat gold surfaces have been investigated using Atomic Force Microscopy (AFM). AFM nanoshaving experiments, performed in hard tapping mode, allowed selectively removing molecules from micro-sized regions. To image the shaved areas, in addition to the soft contact mode, we explored the use of the Quantitative Imaging (QI) mode. QI is a less perturbative imaging mode that allows obtaining quantitative information on both sample topography and mechanical properties. AFM analysis showed that DNA SAMs assembled at high ionic strength are thicker and less deformable than films prepared at low ionic strength. In the case of thicker films, the difference between film and substrate Young’s moduli could be assessed from the analysis of QI data. The AFM finding of thicker and denser films was confirmed by X-Ray Photoelectron Spectroscopy (XPS) and Spectroscopic Ellipsometry (SE) analysis. SE data allowed detecting the DNA UV absorption on dense monomolecular films. Moreover, feeding the SE analysis with the thickness data obtained by AFM, we could estimate the refractive index of dense DNA films.

Highlights

  • Nucleic acid microarrays are largely employed in biosensing: the parallel detection of DNA or RNA hybridization allows for the simultaneous multiple detection of biomarkers [1,2]

  • Examples are the detection of methicillin-resistant Staphylococcus aureus (MRSA) [4], mi-RNA sequences related to tumor or cardiovascular diseases [5,6], or coronavirus-related sequences [7,8]

  • We investigated the role of ionic strength on the morphological and mechanical properties of thiolated DNA SAMs on flat gold substrates

Read more

Summary

Introduction

Nucleic acid microarrays are largely employed in biosensing: the parallel detection of DNA or RNA hybridization allows for the simultaneous multiple detection of biomarkers [1,2]. Hybridization can be exploited for biosensing on a two-fold level It can be used for the direct recognition of specific target sequences, with applications in molecular biology and molecular diagnostics, since particular diseases can be identified based on the identification of specific nucleic acid sequences. Examples are the detection of methicillin-resistant Staphylococcus aureus (MRSA) [4], mi-RNA sequences related to tumor or cardiovascular diseases [5,6], or coronavirus-related sequences [7,8]. In this respect, in response to the pandemic COVID-19 emergency, the selective recognition of SARS-CoV-2 sequences has been recently demonstrated using a thermoplasmonic approach based on DNA hybridization [9]

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call