Enhanced diffusion and enzyme dissociation
Ah-Young Jee, Kuo Chen, Tsvi Tlusty, Jiang Zhao, Steve Granick

TL;DR
This study demonstrates that oligomeric enzymes like urease dissociate into smaller, faster-diffusing subunits at high substrate concentrations, providing a physical explanation for enhanced diffusion observed during catalysis.
Contribution
The paper reveals that enzyme dissociation into subunits explains enhanced diffusion, supported by multiple analytical techniques, challenging previous assumptions about enzyme motion.
Findings
Urease dissociates into subunits at high substrate concentrations.
Enzymatic catalysis enhances diffusion below kM without dissociation.
Multiple analytical methods confirm enzyme dissociation and diffusion changes.
Abstract
The concept that catalytic enzymes can act as molecular machines transducing chemical activity into motion has conceptual and experimental support, but much of the claimed support comes from experimental conditions where the substrate concentration is higher than biologically relevant and accordingly exceeds kM, the Michaelis-Menten constant. Moreover, many of the enzymes studied experimentally to date are oligomeric. Urease, a hexamer of subunits, has been considered to be the gold standard demonstrating enhanced diffusion. Here we show that urease and certain other oligomeric enzymes of high catalytic activity above kM dissociate into their smaller subunit fragments that diffuse more rapidly, thus providing a simple physical mechanism of enhanced diffusion in this regime of concentrations. Mindful that this conclusion may be controversial, our findings are sup-ported by four…
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