Un-“ESCRT”-ed Budding

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Un-“ESCRT”-ed Budding

In their recent publication, Rossman et al. describe how the inherent budding capability of its M2 protein allows influenza A virus to bypass recruitment of the cellular ESCRT machinery enlisted by several other enveloped RNA and DNA viruses, including HIV, Ebola, rabies, herpes simplex type 1 and hepatitis B. Studies from the same laboratory and other laboratories indicate that budding of plas...

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The ESCRT pathway and HIV-1 budding.

HIV-1 Gag engages components of the ESCRT (endosomal sorting complex required for transport) pathway via so-called L (late-assembly) domains to promote virus budding. Specifically, the PTAP (Pro-Thr-Ala-Pro)-type primary L domain of HIV-1 recruits ESCRT-I by binding to Tsg101 (tumour susceptibility gene 101), and an auxiliary LYPX(n)L (Leu-Tyr-Pro-Xaa(n)-Leu)-type L domain recruits the ESCRT-II...

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Role of ESCRT-I in retroviral budding.

Retroviral late-budding (L) domains are required for the efficient release of nascent virions. The three known types of L domain, designated according to essential tetrapeptide motifs (PTAP, PPXY, or YPDL), each bind distinct cellular cofactors. We and others have demonstrated that recruitment of an ESCRT-I subunit, Tsg101, a component of the class E vacuolar protein sorting (VPS) machinery, is...

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Un Co Rr Ect Ed Pr Oo

12 Article Chronology: 13 Received 30 August 2006 14 Revised version received 15 26 December 2006 16 Accepted 23 January 2007 7 The coxsackie and adenovirus receptor (CAR), a putative cell–cell adhesion molecule, has 8 attracted wide interest due to its importance in viral pathogenesis and in mediating 9 adenoviral gene delivery. However, the distribution pattern and physiological function of 2...

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Release of autoinhibition converts ESCRT-III components into potent inhibitors of HIV-1 budding.

The endosomal sorting complex ESCRT-III, which is formed by the structurally related CHMP proteins, is engaged by HIV-1 to promote viral budding. Here we show that progressive truncations into the C-terminal acidic domains of CHMP proteins trigger an increasingly robust anti-HIV budding activity. Together with biochemical evidence for specific intramolecular interactions between the basic and a...

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ژورنال

عنوان ژورنال: Viruses

سال: 2011

ISSN: 1999-4915

DOI: 10.3390/v3010026