Programmable DNA order/disorder modulates phase behavior and dynamics of DNA/peptide condensates

Membraneless compartments formed by liquid–liquid phase separation (LLPS) regulate biochemical reactions and play a key role in both physiological and pathological processes, including viral replication. In retroviral systems, the extent of genome folding is critical for the efficient packaging of new viral particles, a process mediated by the nucleocapsid (NC) protein that chaperones RNA folding and assembly. Here, we sought to elucidate how nucleic-acid folding and structural order/disorder influence LLPS, and whether an HIV NC-derived peptide (HNP) can modulate this process through chaperone-like activity. To this end, we designed a programmable single-stranded DNA (ssDNA) library spanning varying degree of ordered/disordered and palindromic architectures, enabling systematic investigation of how nanoscale structural order governs coacervation. Using circular dichroism, FRET, SAXS, and coarse-grained simulations, we correlate DNA conformations with phase behavior and emergent condensate material properties. We find that interactions with HNP promote DNA folding, and that increasing DNA order suppresses LLPS, whereas structural disorder and palindromic linkers that induce DNA dimerization enhance phase separation by facilitating multivalent interactions and in turn, increasing condensate viscosity. Together, these findings identify two programmable determinants, local structural order and palindromic dimerization, that govern DNA/peptide condensate behavior, offering mechanistic insight into viral genome organization and guiding principles for tuning the physicochemical and material properties of synthetic condensates.