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<p>Bacteriophage T4 has long served as an extraordinary model for tailed phages. During virion assembly, the viral DNA genome is tightly packed into the head, to which tail attaches via a portal-neck connector. Keeping this highly pressurized head leak-proof during these transactions is a challenge, yet the mechanisms remain poorly understood. Here we show that T4 seals its DNA-filled capsid using a double “genome-gate” mechanism. By reconstituting portal (gp20)–neck (gp13/gp14) assembly intermediates in vitro and determining their structures, we find that the gp14 hexamer forms a primary gate that closes the portal-neck opening. This gate is reinforced by a second gate formed by the host protein Hfq, which is hijacked by the virus as an accessory structural component. Hfq also stabilizes neck assembly and prevents its mis-assembly with portal. These studies define a viral genome retention mechanism in which a pre-assembled gp13/gp14/Hfq neck complex seals the pressurized, genome-filled capsid during virion maturation.</p>

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Cryo-EM structures of bacteriophage T4 portal-neck assembly intermediates reveal a viral genome retention mechanism

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年2月7日

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  • Lin Han,
  • Qiyu Mao,
  • Jingen Zhu,
  • Xiaohui Jin,
  • Xiaodan Wang,
  • Zhimin Liu,
  • Narbada Upreti,
  • Xiaorong Wu,
  • Qianglin Fang,
  • Andrei Fokine,
  • Venigalla B. Rao,
  • Zhenguo Chen,
  • Lei Sun

摘要

Bacteriophage T4 has long served as an extraordinary model for tailed phages. During virion assembly, the viral DNA genome is tightly packed into the head, to which tail attaches via a portal-neck connector. Keeping this highly pressurized head leak-proof during these transactions is a challenge, yet the mechanisms remain poorly understood. Here we show that T4 seals its DNA-filled capsid using a double “genome-gate” mechanism. By reconstituting portal (gp20)–neck (gp13/gp14) assembly intermediates in vitro and determining their structures, we find that the gp14 hexamer forms a primary gate that closes the portal-neck opening. This gate is reinforced by a second gate formed by the host protein Hfq, which is hijacked by the virus as an accessory structural component. Hfq also stabilizes neck assembly and prevents its mis-assembly with portal. These studies define a viral genome retention mechanism in which a pre-assembled gp13/gp14/Hfq neck complex seals the pressurized, genome-filled capsid during virion maturation.