Distinct stabilization of the human T cell leukemia virus type 1 immature Gag lattice

Human T cell leukemia virus type 1 (HTLV-1) immature particles differ in morphology from other retroviruses, suggesting a distinct way of assembly. Here we report the results of cryo-electron tomography studies of HTLV-1 virus-like particles assembled in vitro, as well as derived from cells. This work shows that HTLV-1 uses a distinct mechanism of Gag-Gag interactions to form the immature viral lattice. Analysis of high-resolution structural information from immature capsid (CA) tubular arrays reveals that the primary stabilizing component in HTLV-1 is the N-terminal domain of CA. Mutagenesis analysis supports this observation. This distinguishes HTLV-1 from other retroviruses, in which the stabilization is provided primarily by the C-terminal domain of CA. These results provide structural details of the quaternary arrangement of Gag for an immature deltaretrovirus and this helps explain why HTLV-1 particles are morphologically distinct.

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Publication Details

Journal
Nature Structural & Molecular Biology
Published
2024-09-06
DOI
https://doi.org/10.1038/s41594-024-01390-8
Citations
9
Primary Topic
T-cell and Retrovirus Studies
Type
article
Field-Weighted Citation Impact
2.16
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article

Distinct stabilization of the human T cell leukemia virus type 1 immature Gag lattice

Gergely Pinke, Robert A. Dick, Darya Chernikova, Martin Obr et al.
9 citations
Nature Structural & Molecular Biology
T-cell and Retrovirus Studies
2.16
article

Distinct stabilization of the human T cell leukemia virus type 1 immature Gag lattice

Gergely Pinke, Robert A. Dick, Darya Chernikova, Martin Obr, Huixin Yang, A. Thader, Louis M. Mansky, Mathias Percipalle, Darío Porley, F.K.M. Schur
article en
9 citations

Abstract

Human T cell leukemia virus type 1 (HTLV-1) immature particles differ in morphology from other retroviruses, suggesting a distinct way of assembly. Here we report the results of cryo-electron tomography studies of HTLV-1 virus-like particles assembled in vitro, as well as derived from cells. This work shows that HTLV-1 uses a distinct mechanism of Gag-Gag interactions to form the immature viral lattice. Analysis of high-resolution structural information from immature capsid (CA) tubular arrays reveals that the primary stabilizing component in HTLV-1 is the N-terminal domain of CA. Mutagenesis analysis supports this observation. This distinguishes HTLV-1 from other retroviruses, in which the stabilization is provided primarily by the C-terminal domain of CA. These results provide structural details of the quaternary arrangement of Gag for an immature deltaretrovirus and this helps explain why HTLV-1 particles are morphologically distinct.

Nature Structural & Molecular BiologyVol. 32(2)
University of Minnesota (US), Emory University (US), Institute of Science and Technology Austria (AT), Cornell University (US), Thermo Fisher Scientific (Netherlands) (NL)
Openalex Percentile: Top 12%
T-cell and Retrovirus Studies
2.16
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Distinct stabilization of the human T cell leukemia virus type 1 immature Gag lattice — Gergely Pinke, Robert A. Dick, et al. · Nature Structural & Molecular Biology (2024) | TGRS Research Map | TGRS