9G54

Group II intron assembly intermediate Domain 1, 2, 3 and 4 "Partly open" state

9G54 の概要

• エントリーDOI: 10.2210/pdb9g54/pdb
• EMDBエントリー: 51077
• 分子名称: GROUP IIC INTRON (1 entity in total)
• 機能のキーワード: rna folding, protein-free rna cryo-em, ribozyme, metalloenzymes, splicing, rna
• 由来する生物種: Oceanobacillus iheyensis
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 117573.62

構造登録者

Jadhav, S.S.,Marcia, M. (登録日: 2024-07-16, 公開日: 2025-11-05, 最終更新日: 2025-12-10)

主引用文献

Jadhav, S.,Maiorca, M.,Manigrasso, J.,Saha, S.,Rakitch, A.,Muscat, S.,Mulvaney, T.,De Vivo, M.,Topf, M.,Marcia, M.
Dynamic assembly of a large multidomain ribozyme visualized by cryo-electron microscopy.
Nat Commun, 16:10195-10195, 2025

PubMed Abstract: Many RNAs rely on their 3D structures for function. While acquiring functional 3D structures, certain RNAs form misfolded, non-functional states ('kinetic traps'). Instead, other RNAs sequentially assemble into their functional conformations over pre-folded scaffolds. Elucidating the principles of RNA sequential assembly is thus important to understand how RNAs avoid the formation of misfolded, non-functional states. Integrating single-particle electron cryomicroscopy (cryo-EM), image processing, in solution small-angle X-ray scattering (SAXS), EM-driven molecular dynamics (MD) simulations, structure-based mutagenesis, and enzymatic assays, we have visualized the sequential multidomain assembly of a self-splicing ribozyme of biomedical and bioengineering significance. Our work reveals a distinct dynamic interplay of helical subdomains in the ribozyme's 5'-terminal scaffold, which acts as a gate to control the docking of 3'-terminal domains. We identify specific conserved and functionally important secondary structure motifs as the key players for orchestrating the energetically inexpensive conformational changes that lead to the productive formation of the catalytic pocket. Our work provides a near-atomic resolution molecular movie of a large multidomain RNA assembling into its functionally active conformation and establishes a basis for understanding how RNA avoids the formation of non-functional 'kinetic traps'.

PubMed: 41309593
DOI: 10.1038/s41467-025-65502-8

実験手法

ELECTRON MICROSCOPY (6.3 Å)