We investigate the Brownian dynamics of a nanoparticle bound to a thermally undulating elastic membrane. The ligand-functionalized nanoparticle is assumed to interact monovalently with the receptor expressed on the membrane. In order to resolve the nanoparticle transient motion subject to the instantaneous membrane configuration in a consistent manner, we employ a set of coupled Langevin equations that simultaneously incorporate the hydrodynamic effects, ligand-receptor binding interaction, intramembrane elastic forces, and thermal fluctuations. We show that the presence of a deformable, elastic fluid membrane not only affects the dynamics of a bound nanoparticle but also alters the effective binding potential felt by the nanoparticle. In contrast to a nanoparticle bound to a flat surface, the oscillatory characteristics of the nanoparticle velocity autocorrelation function are suppressed and transition to an anticorrelated long-time tail. Moreover, the nanoparticle position fluctuation becomes more coherent with that of the membrane binding site, and the width of the distribution of the nanoparticle distance from the membrane decreases with increasing membrane bending rigidity. By introducing a locally harmonic, bistable potential as an effective potential for the ligand-receptor pair, the rate of nanoparticle transitioning between two bound states is facilitated by membrane undulations as a result of stronger positional variations associated with the nanoparticle.

• Received 5 November 2019
• Accepted 21 February 2020

DOI:https://doi.org/10.1103/PhysRevE.101.032604