Department of Neuroscience, Physiology and Pharmacology, University College London, London, UK.
Department of Microbiology and Translational Data Analytics Institute, The Ohio State University, Columbus, OH, USA.
Channels (Austin). 2023 Dec;17(1):2167563. doi: 10.1080/19336950.2023.2167563.
In this hybrid review, we have first collected and reviewed available information on the structure and function of the enigmatic cache domains in αδ proteins. These are organized into two double cache (dCache_1) domains, and they are present in all αδ proteins. We have also included new data on the key function of these domains with respect to amino acid and gabapentinoid binding to the universal amino acid-binding pocket, which is present in αδ-1 and αδ-2. We have now identified the reason why αδ-3 and αδ-4 do not bind gabapentinoid drugs or amino acids with bulky side chains. In relation to this, we have determined that the bulky amino acids Tryptophan and Phenylalanine prevent gabapentin from inhibiting cell surface trafficking of αδ-1. Together, these novel data shed further light on the importance of the cache domains in αδ proteins.
在这篇混合综述中,我们首先收集并回顾了关于 αδ 蛋白中神秘的缓存结构域的结构和功能的现有信息。这些结构域组织成两个双缓存 (dCache_1) 域,存在于所有 αδ 蛋白中。我们还纳入了关于这些结构域关键功能的新数据,这些数据与氨基酸和加巴喷丁类药物结合到普遍存在于 αδ-1 和 αδ-2 中的氨基酸结合口袋有关。我们现在已经确定了 αδ-3 和 αδ-4 为什么不结合加巴喷丁类药物或具有大侧链的氨基酸的原因。关于这一点,我们已经确定大的氨基酸色氨酸和苯丙氨酸阻止加巴喷丁抑制 αδ-1 的细胞表面转运。总之,这些新数据进一步阐明了缓存结构域在 αδ 蛋白中的重要性。