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Implications of dimeric activation of PDE6 for rod phototransduction
We examine the implications of a recent report providing evidence that two transducins must bind to the rod phosphodiesterase to elicit significant hydrolytic activity. To predict the rod photoreceptor's electrical response, we use numerical simulation of the two-dimensional diffusional contact...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119862/ https://www.ncbi.nlm.nih.gov/pubmed/30068567 http://dx.doi.org/10.1098/rsob.180076 |
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author | Lamb, Trevor D. Heck, Martin Kraft, Timothy W. |
author_facet | Lamb, Trevor D. Heck, Martin Kraft, Timothy W. |
author_sort | Lamb, Trevor D. |
collection | PubMed |
description | We examine the implications of a recent report providing evidence that two transducins must bind to the rod phosphodiesterase to elicit significant hydrolytic activity. To predict the rod photoreceptor's electrical response, we use numerical simulation of the two-dimensional diffusional contact of interacting molecules at the surface of the disc membrane, and then we use the simulated PDE activity as the driving function for the downstream reaction cascade. The results account for a number of aspects of rod phototransduction that have previously been puzzling. For example, they explain the existence of a greater initial delay in rods than in cones. Furthermore, our analysis suggests that the ‘continuous’ noise recorded in rods in darkness is likely to arise from spontaneous activation of individual molecules of PDE at a rate of a few tens per second per rod, probably as a consequence of spontaneous activation of transducins at a rate of thousands per second per rod. Hence, the dimeric activation of PDE in rods provides immunity against spontaneous transducin activation, thereby reducing the continuous noise. Our analysis also provides a coherent quantitative explanation of the amplification underlying the single photon response. Overall, numerical analysis of the dimeric activation of PDE places rod phototransduction in a new light. |
format | Online Article Text |
id | pubmed-6119862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-61198622018-09-06 Implications of dimeric activation of PDE6 for rod phototransduction Lamb, Trevor D. Heck, Martin Kraft, Timothy W. Open Biol Research We examine the implications of a recent report providing evidence that two transducins must bind to the rod phosphodiesterase to elicit significant hydrolytic activity. To predict the rod photoreceptor's electrical response, we use numerical simulation of the two-dimensional diffusional contact of interacting molecules at the surface of the disc membrane, and then we use the simulated PDE activity as the driving function for the downstream reaction cascade. The results account for a number of aspects of rod phototransduction that have previously been puzzling. For example, they explain the existence of a greater initial delay in rods than in cones. Furthermore, our analysis suggests that the ‘continuous’ noise recorded in rods in darkness is likely to arise from spontaneous activation of individual molecules of PDE at a rate of a few tens per second per rod, probably as a consequence of spontaneous activation of transducins at a rate of thousands per second per rod. Hence, the dimeric activation of PDE in rods provides immunity against spontaneous transducin activation, thereby reducing the continuous noise. Our analysis also provides a coherent quantitative explanation of the amplification underlying the single photon response. Overall, numerical analysis of the dimeric activation of PDE places rod phototransduction in a new light. The Royal Society 2018-08-01 /pmc/articles/PMC6119862/ /pubmed/30068567 http://dx.doi.org/10.1098/rsob.180076 Text en © 2018 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Lamb, Trevor D. Heck, Martin Kraft, Timothy W. Implications of dimeric activation of PDE6 for rod phototransduction |
title | Implications of dimeric activation of PDE6 for rod phototransduction |
title_full | Implications of dimeric activation of PDE6 for rod phototransduction |
title_fullStr | Implications of dimeric activation of PDE6 for rod phototransduction |
title_full_unstemmed | Implications of dimeric activation of PDE6 for rod phototransduction |
title_short | Implications of dimeric activation of PDE6 for rod phototransduction |
title_sort | implications of dimeric activation of pde6 for rod phototransduction |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6119862/ https://www.ncbi.nlm.nih.gov/pubmed/30068567 http://dx.doi.org/10.1098/rsob.180076 |
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