Year: 2026
Type: article
Abstract: Recent experimental evidence has shown that enzymes that catalyze exergonic reactions are able to diffuse faster during catalysis, a process called "enhanced diffusion". If true, enzyme propulsion could enable the engineering of designed active materials at the nanoscale. However, further experimental validation is needed under well-controlled conditions. We use single-molecule tracking of enzymes tethered to fluid lipid bilayers, which serve to constrain motion to two dimensions, lower baseline diffusion for improved sensitivity, and accommodate multiple tethering strategies. We find that active urease diffuses approximately 40% faster in the presence of substrate (urea) than in its absence or when inhibited, independent of the tethering scheme. The degree of enhancement scales with the substrate concentration, consistent with prior studies. Finally, we find that assembling multiple enzymes into larger complexes results in even greater diffusion enhancement. This work indicates that enzymes could serve as a platform to create and study active particles at the nanoscale.
Source: Nano Letters
Authors: Ashley Scott, Mengqi Xu, Ian Murphy, David S.-J. Jang, Zainab Marwa Rana, Anthony Estrada, Wylie W. Ahmed, W. Benjamin Rogers, Jennifer L. Ross
Language: English
Topic: Micro and Nano Robotics
Subfield: Condensed Matter Physics
Field: Physics and Astronomy
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $4,500
Awards: G1029376177, G1265426323, Collaborative Research: Enzyme-Powered, Programmable Active Matter, G1943680171, Collaborative Research: Enzyme-Powered, Programmable Active Matter, G2646491576, G3923093550, G4740333214, REU Site: Using Microscopy to understand Form and Function Across Biological Scales (MicroFFABS), Research - Syracuse University (2024), Collaborative Research: Enzyme-Powered, Programmable Active Matter
OpenAlex ID: W7128913678
