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.
Authors
- Gergely Pinke (ORCID: https://orcid.org/0000-0002-6727-7296)
- Robert A. Dick (ORCID: https://orcid.org/0000-0003-3693-2531)
- Darya Chernikova (ORCID: https://orcid.org/0009-0007-4866-8498)
- Martin Obr (ORCID: https://orcid.org/0000-0003-1756-6564)
- Huixin Yang (ORCID: https://orcid.org/0000-0003-0539-0477)
- A. Thader (ORCID: https://orcid.org/0000-0001-6966-0400)
- Louis M. Mansky (ORCID: https://orcid.org/0000-0003-2391-1061)
- Mathias Percipalle (ORCID: https://orcid.org/0009-0006-4081-1571)
- Darío Porley
- F.K.M. Schur (ORCID: https://orcid.org/0000-0003-4790-8078)
Institutions
- University of Minnesota (US)
- Emory University (US)
- Institute of Science and Technology Austria (AT)
- Cornell University (US)
- Thermo Fisher Scientific (Netherlands) (NL)
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