Discrimination between Functional and Non-functional Cellular Gag Complexes involved in HIV-1 Assembly

HIV-1 Gag and Gag-Pol are responsible for viral assembly and maturation and represent a major paradigm for enveloped virus assembly. Numerous intracellular Gag-containing complexes (GCCs) have been identified in cellular lysates using sucrose gradient ultracentrifugation. While these complexes are universally present in Gag-expressing cells, their roles in virus assembly are not well understood. Here we demonstrate that most GCC species are predominantly comprised of monomeric or dimeric Gag molecules bound to ribosomal complexes, and as such, are not on-pathway intermediates in HIV assembly. Rather, these GCCs represent a population of Gag that is not yet functionally committed for incorporation into a viable virion precursor. We hypothesize that these complexes act as a reservoir of monomeric Gag that can incorporate into assembling viruses, and serve to mitigate non-specific intracellular Gag oligomerization. We have identified a subset of large GCC complexes, comprising more than 20 Gag molecules, that may be equivalent to membrane-associated puncta previously shown to be bona fide assembling-virus intermediates. This work provides a clear rationale for the existence of diverse GCCs, and serves as the foundation for characterizing on-pathway intermediates early in virus assembly. (C) 2021 Elsevier Ltd. All rights reserved.

Automated summary

Most GCC species are mainly composed of monomeric or dimeric Gag molecules bound to ribosomal complexes, representing a population of Gag not yet functionally committed for incorporation into viable virion precursors. A subset of large GCC complexes, with more than 20 Gag molecules, may be equivalent to membrane-associated puncta as genuine assembling-virus intermediates. These findings provide a rationale for the existence of diverse GCCs and lay the foundation for characterizing on-pathway intermediates in early virus assembly.