Related Experiment Video
Updated: May 24, 2026

13:14
Genetic Barcoding with Fluorescent Proteins for Multiplexed Applications
Published on: April 14, 2015
Electronic barcoding of a viral gene at the single-molecule level
Alon Singer1, Srinivas Rapireddy, Danith H Ly
1Department of Biomedical Engineering, Boston University, Boston, Massachusetts 02215, USA.
Nano Letters
|February 23, 2012
Summary
This study introduces a novel single-molecule method using nanopores and peptide nucleic acid probes for rapid gene discrimination. The technique accurately barcodes genes, enabling quick identification of similar pathogens like HIV subtypes.
Area of Science:
- Biotechnology
- Molecular Biology
- Nanotechnology
Background:
- Accurate and rapid discrimination between similar genes, such as pathogen subtypes, is crucial for diagnostics.
- Existing methods may lack the speed or resolution required for real-time classification.
- Single-molecule analysis offers potential for high-sensitivity detection and differentiation.
Purpose of the Study:
- To develop a novel single-molecule approach for rapid and purely electronic discrimination of similar genes.
- To demonstrate the feasibility of this method for pathogen classification using human immunodeficiency virus (HIV) subtypes as a model.
Main Methods:
- Utilizing solid-state nanopores for molecular confinement and electronic signal transduction.
- Employing γ-modified synthetic peptide nucleic acid (PNA) probes for specific gene barcoding.
- Quantifying gene identity by counting attached probes and measuring their spatial distribution along the molecule.
Main Results:
- Successfully demonstrated a single-molecule approach for gene discrimination based on probe count and spacing.
- Achieved accurate barcoding of individual genes from two highly similar HIV subtypes.
- Validated the electronic detection and classification capabilities of the developed platform.
Conclusions:
- The presented single-molecule, nanopore-based method enables rapid and purely electronic gene discrimination.
- This approach offers a novel diagnostic platform for the fast classification of pathogens, including closely related viral subtypes.
- The technology holds promise for advancing molecular diagnostics and infectious disease surveillance.
Related Concept Videos
RNA-seq
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while microarray-based...
DNA Microarrays
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...

