Analysis of MC Systems Employing Receivers Covered by Heterogeneous Receptors

TL;DR

This paper analyzes the molecule hitting rate of a molecular communication system with heterogeneous receptors on the receiver, considering different transmitter types and receptor distributions, validated by simulations.

Contribution

It provides a novel analytical framework for the expected molecule absorption in MC systems with heterogeneous receptors and arbitrary receptor distributions.

Findings

Absorbed molecules increase with the number of receptors when total receptor area is fixed.

Evenly distributed receptors maximize molecule absorption compared to other distributions.

The analytical model matches particle-based simulation results accurately.

Abstract

This paper investigates the channel impulse response (CIR), i.e., the molecule hitting rate, of a molecular communication (MC) system employing an absorbing receiver (RX) covered by multiple non overlapping receptors. In this system, receptors are heterogeneous, i.e., they may have different sizes and arbitrary locations. Furthermore, we consider two types of transmitter (TX), namely a point TX and a membrane fusion (MF)-based spherical TX. We assume the point TX or the center of the MF-based TX has a fixed distance to the center of the RX. Given this fixed distance, the TX can be at different locations and the CIR of the RX depends on the exact location of the TX. By averaging over all possible TX locations, we analyze the expected molecule hitting rate at the RX as a function of the sizes and locations of the receptors, where we assume molecule degradation may occur during the propagation of the signaling molecules. Notably, our analysis is valid for different numbers, a wide range of sizes, and arbitrary locations of the receptors, and its accuracy is confirmed via particle-based simulations. Exploiting our numerical results, we show that the expected number of absorbed molecules at the RX increases with the number of receptors, when the total area on the RX surface covered by receptors is fixed. Based on the derived analytical expressions, we compare different geometric receptor distributions by examining the expected number of absorbed molecules at the RX. We show that evenly distributed receptors result in a larger number of absorbed molecules than other distributions. We further compare three models that combine different types of TXs and RXs.