6BM8

Crystal structure of glycoprotein B from Herpes Simplex Virus type I

6BM8 の概要

• エントリーDOI: 10.2210/pdb6bm8/pdb
• 関連するPDBエントリー: 5V2S
• 分子名称: Envelope glycoprotein B, beta-D-mannopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose-(1-4)-2-acetamido-2-deoxy-beta-D-glucopyranose, 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: viral protein, fusogen, bitopic membrane protein
• 由来する生物種: Human herpesvirus 1 (HHV-1)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 94981.80

構造登録者

Cooper, R.S.,Heldwein, E.E. (登録日: 2017-11-13, 公開日: 2018-05-16, 最終更新日: 2024-11-06)

主引用文献

Cooper, R.S.,Georgieva, E.R.,Borbat, P.P.,Freed, J.H.,Heldwein, E.E.
Structural basis for membrane anchoring and fusion regulation of the herpes simplex virus fusogen gB.
Nat. Struct. Mol. Biol., 25:416-424, 2018

PubMed Abstract: Viral fusogens merge viral and cell membranes during cell penetration. Their ectodomains drive fusion by undergoing large-scale refolding, but little is known about the functionally important regions located within or near the membrane. Here we report the crystal structure of full-length glycoprotein B (gB), the fusogen from herpes simplex virus, complemented by electron spin resonance measurements. The membrane-proximal (MPR), transmembrane (TMD), and cytoplasmic (CTD) domains form a uniquely folded trimeric pedestal beneath the ectodomain, which balances dynamic flexibility with extensive, stabilizing membrane interactions. The postfusion conformation of the ectodomain suggests that the CTD likewise adopted the postfusion form. However, hyperfusogenic mutations, which destabilize the prefusion state of gB, target key interfaces and structural motifs that reinforce the observed CTD structure. Thus, a similar CTD structure must stabilize gB in its prefusion state. Our data suggest a model for how this dynamic, membrane-dependent 'clamp' controls the fusogenic refolding of gB.

PubMed: 29728654
DOI: 10.1038/s41594-018-0060-6

実験手法

X-RAY DIFFRACTION (4.1 Å)