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Biology subjects

Li, C. X.

Publications and source records attributed to Li, C. X..

2 recordsLinked to original sources

Auditory Stimulus Information Entropy Modulates Inter-Brain Synchronization: Evidence from Wireless EEG Hyperscanning

Inter-brain synchronization (IBS) - reflecting inter-individual correlated neural activity during interaction - marks shared experiences like music listening. The ability of complex auditory stimuli (e.g., music) to induce IBS links to their information dynamics, notably the uncertainty they evoke, which challenges the nervous systems predictive coding. Based on mutual prediction theory (interacting individuals simultaneously process their own behavior and predict their partners; accurate mutual predictions lead to convergent neural representations and thus IBS), this study hypothesized that higher stimulus uncertainty enhances IBS (heightened uncertainty reduces independent predictability, promoting convergent representations and stronger IBS). Using information entropy to quantify uncertainty, the study conducted hyperscanning, manipulated entropy across Resting State and 6 Hz auditory stimuli (ASSR, MMN, AHER, Dream Wedding), and measured IBS via phase-locking values (PLV). Results showed frequency specificity: 6 Hz PLV increased with entropy (DW {approx} AHER > MMN {approx} ASSR > Resting State); Alpha band had highest PLV in Resting State. Critically, PLVs differed significantly between any two conditions, and each experimental conditions PLV was also significantly different from that of the Resting State. Findings confirm a 6 Hz-specific positive association between auditory uncertainty and IBS, suggesting musical elements may facilitate social interaction by modulating entropy, with entropy-IBS relations showing frequency dependence.

neuroscience↗

Single-molecule assay reveals the impact of composition, RNA duplex, and inhibitors on the binding dynamics of SARS-CoV-2 polymerase complex

The genome replication of SARS-CoV-2, the causative agent of COVID-19, involves a multi-subunit replication complex consisting of non-structural proteins (nsps) 12, 7 and 8. While the structure of this complex is known, the dynamic behavior of the subunits interacting with RNA is missing. Here we report a single-molecule protein-induced fluorescence enhancement (SM-PIFE) assay to monitor binding dynamics between the reconstituted or co-expressed replication complex and RNA. Increasing binding times were observed, in this order, with nsp7 (none) nsp8 and nsp12, in nsp8-nsp12 mixtures and in reconstituted mixtures bearing all three proteins. Unstable, transient, and stable binding modes were recorded in the latter case, indicating that complexation is dynamic, and the correct conformation must be achieved before stable RNA binding can occur. Notably, the co-expressed protein yields mostly stable binding even at low concentrations, while the reconstituted proteins exhibit unstable binding indicating inefficient complexation with reduced protein. The SM-PIFE assay distinguishes inhibitors that impact protein binding from those that prevent replication, as demonstrated with suramin and remdesivir, respectively. The data reveals a correlation between binding lifetime/affinity, and protein activity, and underscores differences between co-expressed vs reconstituted mixtures, suggesting the existence of trapped conformations that may not evolve to productive binding.

biophysics↗