9F3C

Low-resolution (5.4 angstrom) cryo-EM structure of SV2B-BoNT/A1 at pH 5.5

9F3C の概要

• エントリーDOI: 10.2210/pdb9f3c/pdb
• EMDBエントリー: 50151
• 分子名称: Synaptic vesicle glycoprotein 2B, Botulinum neurotoxin type A, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
• 機能のキーワード: transporter, botulinum neurotoxin, synaptic vesicle glycoprotein, membrane protein
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 2
• 化学式量合計: 231627.71

構造登録者

Khanppnavar, B.,Leka, O.,Korkhov, V.,Kammerer, R. (登録日: 2024-04-25, 公開日: 2025-03-12)

主引用文献

Khanppnavar, B.,Leka, O.,Pal, S.K.,Korkhov, V.M.,Kammerer, R.A.
Cryo-EM structure of the botulinum neurotoxin A/SV2B complex and its implications for translocation.
Nat Commun, 16:1224-1224, 2025

PubMed Abstract: Botulinum neurotoxin A1 (BoNT/A1) belongs to the most potent toxins and is used as a major therapeutic agent. Neurotoxin conformation is crucial for its translocation to the neuronal cytosol, a key process for intoxication that is only poorly understood. To gain molecular insights into the steps preceding toxin translocation, we determine cryo-EM structures of BoNT/A1 alone and in complex with its receptor synaptic vesicle glycoprotein 2B (SV2B). In solution, BoNT/A1 adopts a unique, semi-closed conformation. The toxin changes its structure into an open state upon receptor binding with the translocation domain (H) and the catalytic domain (LC) remote from the membrane, suggesting translocation incompatibility. Under acidic pH conditions, where translocation is initiated, receptor-bound BoNT/A1 switches back into a semi-closed conformation. This conformation brings the LC and H close to the membrane, suggesting that a translocation-competent state of the toxin is required for successful LC transport into the neuronal cytosol.

PubMed: 39934119
DOI: 10.1038/s41467-025-56304-z

実験手法

ELECTRON MICROSCOPY (5.41 Å)