A hybrid stochastic/deterministic model of single photon response and light adaptation in mouse rods

被引:6
作者
Beelen, Charlotte Johanna [1 ]
Asteriti, Sabrina [2 ,3 ]
Cangiano, Lorenzo [2 ]
Koch, Karl-Wilhelm [1 ]
Dell'Orco, Daniele [3 ]
机构
[1] Carl von Ossietzky Univ Oldenburg, Div Biochem, Dept Neurosci, D-26111 Oldenburg, Germany
[2] Univ Pisa, Dept Translat Res, I-56123 Pisa, Italy
[3] Univ Verona, Sect Biol Chem, Dept Neurosci Biomed & Movement Sci, I-37134 Verona, Italy
关键词
Dynamic modeling; Phototransduction; Stochastic simulation; Light adaptation; Systems biology; TRANSDUCIN CIRCUMSTANTIAL EVIDENCE; DARK RHODOPSIN; TRANSIENT COMPLEXES; G-PROTEIN; PHOTOTRANSDUCTION; PHOTORECEPTORS; PHOSPHORYLATION; PHOTORESPONSES; ORGANIZATION; SIMULATION;
D O I
10.1016/j.csbj.2021.06.033
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The phototransduction cascade is paradigmatic for signaling pathways initiated by G protein-coupled receptors and is characterized by a fine regulation of photoreceptor sensitivity and electrical response to a broad range of light stimuli. Here, we present a biochemically comprehensive model of phototransduction in mouse rods based on a hybrid stochastic and deterministic mathematical framework, and a quantitatively accurate description of the rod impedance in the dark. The latter, combined with novel patch clamp recordings from rod outer segments, enables the interconversion of dim flash responses between photovoltage and photocurrent and thus direct comparison with the simulations. The model reproduces the salient features of the experimental photoresponses at very dim and bright stimuli, for both normal photoreceptors and those with genetically modified cascade components. Our modelling approach recapitulates a number of recent findings in vertebrate phototransduction. First, our results are in line with the recently established requirement of dimeric activation of PDE6 by transducin and further show that such conditions can be fulfilled at the expense of a significant excess of G protein activated by rhodopsin. Secondly, simulations suggest a crucial role of the recoverin-mediated Ca2+-feedback on rhodopsin kinase in accelerating the shutoff, when light flashes are delivered in the presence of a light background. Finally, stochastic simulations suggest that transient complexes between dark rhodopsin and transducin formed prior to light stimulation increase the reproducibility of single photon responses. Current limitations of the model are likely associated with the yet unknown mechanisms governing the shutoff of the cascade. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
引用
收藏
页码:3720 / 3734
页数:15
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