8J6M
SIDT1 protein
8J6M の概要
| エントリーDOI | 10.2210/pdb8j6m/pdb |
| EMDBエントリー | 36008 |
| 分子名称 | Green fluorescent protein,SID1 transmembrane family member 1, CHOLESTEROL, ZINC ION, ... (6 entities in total) |
| 機能のキーワード | transport t1, transcription |
| 由来する生物種 | Aequorea victoria 詳細 |
| タンパク質・核酸の鎖数 | 2 |
| 化学式量合計 | 251901.31 |
| 構造登録者 | |
| 主引用文献 | Zhang, J.,Zhan, C.,Fan, J.,Wu, D.,Zhang, R.,Wu, D.,Chen, X.,Lu, Y.,Li, M.,Lin, M.,Gong, J.,Jiang, D. Structural insights into double-stranded RNA recognition and transport by SID-1. Nat.Struct.Mol.Biol., 31:1095-1104, 2024 Cited by PubMed Abstract: RNA uptake by cells is critical for RNA-mediated gene interference (RNAi) and RNA-based therapeutics. In Caenorhabditis elegans, RNAi is systemic as a result of SID-1-mediated double-stranded RNA (dsRNA) across cells. Despite the functional importance, the underlying mechanisms of dsRNA internalization by SID-1 remain elusive. Here we describe cryogenic electron microscopy structures of SID-1, SID-1-dsRNA complex and human SID-1 homologs SIDT1 and SIDT2, elucidating the structural basis of dsRNA recognition and import by SID-1. The homodimeric SID-1 homologs share conserved architecture, but only SID-1 possesses the molecular determinants within its extracellular domains for distinguishing dsRNA from single-stranded RNA and DNA. We show that the removal of the long intracellular loop between transmembrane helix 1 and 2 attenuates dsRNA uptake and systemic RNAi in vivo, suggesting a possible endocytic mechanism of SID-1-mediated dsRNA internalization. Our study provides mechanistic insights into dsRNA internalization by SID-1, which may facilitate the development of dsRNA applications based on SID-1. PubMed: 38664565DOI: 10.1038/s41594-024-01276-9 主引用文献が同じPDBエントリー |
| 実験手法 | ELECTRON MICROSCOPY (2.77 Å) |
構造検証レポート
検証レポート(詳細版)
をダウンロード






