Controlled Protein Translocation in Nanopores for Sequencing Applications

NIH RePORTER · NIH · R21 · $219,055 · view on reporter.nih.gov ↗

Abstract

Project Summary The ultimate goal in the field of proteomics is single-molecule, high-accuracy, de novo protein sequencing. Unfortunately, current proteomics technologies are costly, and lack the sensitivity, dynamic range, throughput, scale, and accuracy needed to meet this goal. During this project, we will begin examining the technological components and methods required to enable state-of-the-art protein sequencing and characterization. More specifically, we will develop methods for controllably translocating a protein through a nanopore reader such that the protein can be sequenced. Nanopore-based sequencing provides a path to characterizing both high- and low-abundance proteins by sequencing proteins one molecule at a time, but with high accuracy, sensitivity and throughput needed to cover the wide dynamic range in protein abundance in the proteome. During this project, we will develop a completely new nanopore-based technology for de novo protein sequencing. We will develop and build a novel protein sequencing system prototype, fully assess and optimize the associated workflow/methodology for highly controlled and versatile protein/peptide characterization, and demonstrate initial sequencing for various proteins and peptides. At the conclusion of this project, we will have successfully demonstrated feasibility for a practical nanopore-based protein sequencing concept.

Key facts

NIH application ID
10878689
Project number
5R21GM148844-02
Recipient
ELECTRONIC BIOSCIENCES, INC.
Principal Investigator
Eric Mayo Peterson
Activity code
R21
Funding institute
NIH
Fiscal year
2024
Award amount
$219,055
Award type
5
Project period
2023-07-01 → 2026-06-30