An investigation into the feasibility of myoglobin-based single-electron transistors
Debin Li, Peter M. Gannet, and David Lederman

TL;DR
This study explores the use of myoglobin proteins in single-electron transistors, demonstrating that proteins with redox centers can facilitate electron transport and serve as components in nanoscale electronic devices.
Contribution
It provides the first proof-of-principle that proteins with redox centers can be used to create single-electron transistors, highlighting the role of protein structure in device performance.
Findings
Single-electron transport mediated by resonant tunneling through heme groups.
Protein orientation and conformation significantly influence conductance.
Proof-of-principle for protein-based single-electron transistors.
Abstract
Myoglobin single-electron transistors were investigated using nanometer- gap platinum electrodes fabricated by electromigration at cryogenic temperatures. Apomyoglobin (myoglobin without heme group) was used as a reference. The results suggest single electron transport is mediated by resonant tunneling with the electronic and vibrational levels of the heme group in a single protein. They also represent a proof-of-principle that proteins with redox centers across nanometer-gap electrodes can be utilized to fabricate single-electron transistors. The protein orientation and conformation may significantly affect the conductance of these devices. Future improvements in device reproducibility and yield will require control of these factors.
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