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Jiang, h.

Publications and source records attributed to Jiang, h..

2 recordsLinked to original sources

Optical Conductivity as a Stage-Sensitive Imaging Biomarker for Alzheimer's Disease

1.Early detection of Alzheimers disease (AD) remains limited by the inability of current imaging biomarkers to capture dynamic tissue changes preceding overt neurodegeneration. Conventional approaches primarily reflect molecular burden or structural atrophy and incompletely characterize the intermediate microenvironmental remodeling linking early pathology to clinical progression. Here, we introduce optical conductivity as a novel imaging biomarker characterizing tissue responses to optical-frequency electromagnetic fields. Using an optical wave tomography (OWT) framework, optical conductivity is reconstructed from diffuse optical measurements by integrating absorption-driven energy deposition with microstructure-dependent field redistribution. Applied to an APP/PS1 mouse model across young and old cohorts, optical conductivity revealed a significant age-by-disease interaction (F = 9.20, p = 0.0071). Quantitatively, its value was reduced in young AD animals relative to controls ([~]13%; Cohens d = 1.93) but showed attenuation or reversal in older animals, indicating a stage-dependent crossover. Consistently, optical conductivity achieved strong classification performance in the young cohort (AUC = 0.80), outperforming absorption and exceeding scattering, with improved performance via multimodal integration (AUC = 0.87). Together, these findings suggest that optical conductivity captures stage-dependent microenvironmental remodeling not detectable by conventional optical parameters, offering potential for early detection and disease staging.

bioengineering↗

Structural Basis for the Inhibition of the RNA-Dependent RNA Polymerase from SARS-CoV-2 by Remdesivir

The pandemic of Corona Virus Disease 2019 (COVID-19) caused by SARS-CoV-2 has become a global crisis. The replication of SARS-CoV-2 requires the viral RNA-dependent RNA polymerase (RdRp), a direct target of the antiviral drug, Remdesivir. Here we report the structure of the SARS-CoV-2 RdRp either in the apo form or in complex with a 50-base template-primer RNA and Remdesivir at a resolution range of 2.5-2.8 [A]. The complex structure reveals that the partial double-stranded RNA template is inserted into the central channel of the RdRp where Remdesivir is incorporated into the first replicated base pair and terminates the chain elongation. Our structures provide critical insights into the working mechanism of viral RNA replication and a rational template for drug design to combat the viral infection.

molecular biology↗