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Abstract

Intrinsically disordered regions (IDRs) are vital for several cellular processes. They play a significant role in liquid-liquid phase separation (LLPS). LLPS enhances reaction efficiency by locally concentrating proteins and nucleic acids. The BACH2 transcription factor contains such IDRs. Early observations hinted at the phase separation capabilities of BACH2. However, how BACH2-IDR directly participates in LLPS is not fully understood. Its precise modulation by heme binding and phosphorylation also requires further elucidation. This study experimentally demonstrated the intrinsic capability of BACH2-IDR (residues 331-520) to undergo LLPS in vitro. Microscopic observations revealed that TANK-binding kinase 1(TBK1)-mediated phosphorylation suppressed LLPS of BACH2-IDR. Conversely, the coexistence of heme enhanced LLPS, initiating LLPS at lower polyethylene glycol concentrations. Bioinformatic analyses supported these experimental observations. Tools such as FuzDrop and CIDER were used to predict LLPS propensity from sequences. Specifically, the calculations for the sequence of phosphorylation-mimic mutations showed changes in LLPS-promoting regions. Heme binding influenced TBK1-mediated phosphorylation sites. Some of these sites overlap with predicted LLPS-driving regions. Heme binding also induced substantial conformational alterations within BACH2-IDR. Consequently, we propose LLPS as a fundamental regulatory mechanism for BACH2 protein function. This process complements its known regulation through heme binding and phosphorylation.