Abstract

In the human retina, rod and cone cells detect incoming light with a molecule called rhodopsin. After rhodopsin molecules are activated (by photon impact), these molecules activate the rest of the signalling process for a brief period of time until they are deactivated by a multistage process. First, active rhodopsin is phosphorylated multiple times. Following this, they are further inhibited by the binding of molecules called arrestins. Finally, they decay into opsins. The time required for each of these stages becomes progressively longer, and each stage further reduces the activity of rhodopsin. However, while this deactivation process itself is well researched, the roles of the above stages in signal (and image) processing are poorly understood. In this paper, we will show that the activity of rhodopsin molecules during the deactivation process can be described as the fractional integration of an incoming signal. Furthermore, we show how this affects an image; specifically, the effect of fractional integration in video and signal processing and how it reduces noise and the improves adaptability under different lighting conditions. Our experimental results provide a better understanding of vertebrate and human vision, and why the rods and cones of the retina differ from the light detectors in cameras.

Highlights

  • As humans rely heavily on visual perception, research on human vision is currently receiving strong interest

  • We have shown how rhodopsin’s ability to activate the rest of the signalling approximates a fractional integral

  • We have shown how this affects the rest of the signalling process; namely, it improves the cone cells’ abilities to adapt to different light conditions and reduces noise in “measuring” the number of incoming photons

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Summary

Introduction

As humans rely heavily on visual perception, research on human vision is currently receiving strong interest. Despite the rich literature and constant progress in this field, human vision is still not understood in its entirety owing to its overall complexity [1,2,3,4,5] This fact is well illustrated by the different scales of interactions that are required to produce a signal in the retina: (i) molecular processes within the photoreceptor cells [6,7,8]; (ii) the various roles of the photoreceptor cells [9, 10]; (iii) their interactions with other cells before the signal leaves the retina [11,12,13].

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