Nucleotide‐Driven Molecular Sensing of Monkeypox Virus Through Hierarchical Self‐Assembly of 2D Hafnium Disulfide Nanoplatelets and Gold Nanospheres

Author:

Moitra Parikshit12,Iftesum Maria3,Skrodzki David24,Paul Priyanka2,Sheikh Elnaz3,Gray Jennifer Lynn4,Dighe Ketan256,Sheffield Zach25,Gartia Manas Ranjan3,Pan Dipanjan12456ORCID

Affiliation:

1. Department of Nuclear Engineering The Pennsylvania State University University Park PA 16802 USA

2. Department of Pediatrics Centre of Blood Oxygen Transport & Hemostasis University of Maryland Baltimore School of Medicine Baltimore MD 21201 USA

3. 3261 Patrick F Taylor Hall Department of Mechanical & Industrial Engineering Louisiana State University Baton Rouge LA 70803 USA

4. Department of Materials Science and Engineering The Pennsylvania State University University Park PA 16802 USA

5. Department of Chemical & Biochemical Engineering University of Maryland Baltimore County Baltimore County MD 21250 USA

6. Department of Biomedical Engineering The Pennsylvania State University University Park PA 16802 USA

Abstract

AbstractLiquid interfaces facilitate the organization of nanometer‐scale biomaterials with plasmonic properties suitable for molecular diagnostics. Using hierarchical assemblage of 2D hafnium disulfide nanoplatelets and zero‐dimensional spherical gold nanoparticles, the design of a multifunctional material is reported. When the target analyte is present, the nanocomposites’ self‐assembling pattern changes, altering their plasmonic response. Using monkeypox virus (MPXV) as an example, the findings reveal that adding genomic DNA to the nanocomposite surface increases the agglomeration between gold nanoparticles and decreases the π‐stacking distance between hafnium disulfide nanoplatelets. Further, this self‐assembled nanomaterial is found to have minimal cross‐reactivity toward other pathogens and a limit of detection of 7.6 pg µL−1 (i.e., 3.57 × 104 copies µL−1) toward MPXV. Overall, this study helped to gain a better understanding of the genomic organization of MPXV to chemically design and develop targeted nucleotides. The study has been validated by UV–vis spectroscopy, X‐ray diffraction, scanning transmission electron microscopy, surface‐enhanced Raman microscopy and electromagnetic simulation studies. To the best knowledge, this is the first study in literature reporting selective molecular detection of MPXV within a few minutes and without the use of any high‐end instrumental techniques like polymerase chain reactions.

Funder

Centers for Disease Control and Prevention

National Institutes of Health

National Science Foundation

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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