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An Engineered OmpG Nanopore with Displayed Peptide Motifs for Single-Molecule Multiplex Protein Detection
Authors:Joshua C. Foster  Bach Pham  Ryan Pham  Minji Kim  Prof. Matthew D. Moore  Prof. Min Chen
Affiliation:1. Molecular and Cellular Biology Program, University of Massachusetts Amherst, Amherst, MA 01003 USA;2. Department of Chemistry, University of Massachusetts Amherst, Amherst, MA 01003 USA;3. Department of Food Science, University of Massachusetts Amherst, Amherst, MA 01003 USA
Abstract:Molecular detection via nanopore, achieved by monitoring changes in ionic current arising from analyte interaction with the sensor pore, is a promising technology for multiplex sensing development. Outer Membrane Protein G (OmpG), a monomeric porin possessing seven functionalizable loops, has been reported as an effective sensing platform for selective protein detection. Using flow cytometry to screen unfavorable constructs, we identified two OmpG nanopores with unique peptide motifs displayed in either loop 3 or 6, which also exhibited distinct analyte signals in single-channel current recordings. We exploited these motif-displaying loops concurrently to facilitate single-molecule multiplex protein detection in a mixture. We additionally report a strategy to increase sensor sensitivity via avidity motif display. These sensing schemes may be expanded to more sophisticated designs utilizing additional loops to increase multiplicity and sensitivity.
Keywords:Multiplex  Nanopore  Proteins  Sensors  Single-Molecule Detection
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