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The molecular basis of mechanisms underlying polarization vision

机译:偏振视觉的潜在机制的分子基础

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摘要

The underlying mechanisms of polarization sensitivity (PS) have long remained elusive. For rhabdomeric photoreceptors, questions remain over the high levels of PS measured experimentally. In ciliary photoreceptors, and specifically cones, little direct evidence supports any type of mechanism. In order to promote a greater interest in these fundamental aspects of polarization vision, we examined a varied collection of studies linking membrane biochemistry, protein–protein interactions, molecular ordering and membrane phase behaviour. While initially these studies may seem unrelated to polarization vision, a common narrative emerges. A surprising amount of evidence exists demonstrating the importance of protein–protein interactions in both rhabdomeric and ciliary photoreceptors, indicating the possible long-range ordering of the opsin protein for increased PS. Moreover, we extend this direction by considering how such protein paracrystalline organization arises in all cell types from controlled membrane phase behaviour and propose a universal pathway for PS to occur in both rhabdomeric and cone photoreceptors.
机译:极化灵敏度(PS)的基本机制长期以来仍难以捉摸。对于横纹肌感光体,仍然存在实验测定的高水平PS方面的问题。在睫状体感光体,特别是视锥细胞中,几乎没有直接的证据支持任何类型的机制。为了引起人们对偏振视觉这些基本方面的更大兴趣,我们检查了一系列有关膜生物化学,蛋白质-蛋白质相互作用,分子有序性和膜相行为的研究。尽管最初这些研究似乎与两极分化的视觉无关,但出现了一个共同的叙述。存在大量令人惊讶的证据,证明了在横纹和睫状光感受器中蛋白质之间相互作用的重要性,这表明视蛋白在增加PS方面可能存在长距离排序。此外,我们通过考虑这种蛋白质副晶体组织如何在所有细胞类型中从受控的膜相行为中出现来扩展这个方向,并提出了一种在横纹体和锥体感光体中都存在PS的通用途径。

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