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Summary: Although the determination of the structural basis of potato virus Y (PVY) coat protein (CP) provides the possibility for CP-based antiviral drug design, the role of many specific residues on CP in regulating virion pathogenicity is largely unknown, and fewer small-molecular drugs have been discovered to act on these potential sites. In this study, a series of derivatives of 2,2-dimethyl-2H-chromene are rationally designed by employing a molecular hybridization strategy. We screen a case of phytovirucide C50 that could form a stable H-bond with Ser125 of PVY CP to exert antiviral properties. Ser125 is further identified to be crucial for CP-viral RNA (vRNA) interaction, enabling PVY virion assembly. This interaction can be significantly inhibited through competitive binding with compound C50. The study enhances our understanding of anti-PVY drug mechanisms and provides a basis for developing new CP-targeting virus particle assembly inhibitors.

Background: Previous studies have demonstrated that individuals overestimate the time duration of fear-related stimuli compared with relatively neutral stimuli. However, their physiological and psychological mechanisms behind this effect remain unclear. This study investigates the overestimation the duration perception of fearful faces and its relationship with general cognitive ability (short-term memory, working memory, and attentional inhibition). Method: Emotional pictures were selected from the Chinese Facial Affective Picture System. A total of 85 university students (43 females and 42 males,aged 20–24 years) participated in the experiments at a university. In Experiment 1,a temporal bisection task (300 ms: 1200 ms) was used to explore the effect of perceptual overestimating the duration perception of fearful faces and its relationship with general cognitive abilities (short-term memory, working memory, and attentional inhibition), In Experiment 2, the short and long standard time intervals were set to 1200 ms and 4800 ms, respectively, with the other conditions remaining the same as in Experiment 1. Results: Both experiment revealed that participants overestimated the duration of fearful faces compared with that of neutral faces. Experiment 1 indicated no significant correlation between short-term memory, working memory, attention inhibition tests, and the overestimation effect. Experiment 2 revealed a positive correlation between working memory test scores, short-term memory test scores, and the overestimation effect,as well as temporal sensitivity. Conclusion: Individuals tend to overestimate the duration of fearful faces, and the influence of arousal and memory is modulated by the length of the target time intervals.

The Late Ediacaran Dengying Formation, located in the Sichuan Basin of the northwestern Yangtze Craton, is of significant interest in oil and gas exploration due to its abundant pores and vugs within microbial mound-shoal complexes. However, there is still uncertainty regarding the spatiotemporal distribution and controlling factors of the platform margin. This study comprehensively analyzes the retrogradation pattern of the Dengying Formation platform margin using seismic data, well logs, field outcrops, and petrological characteristics. Our findings reveal that the Dengying Formation strata surrounding the rift basin at the northwestern of the Yangtze Craton can be divided into three main depositional facies: basin facies, slope facies, and platform margin facies. Additionally, based on the integration of lithological, log, and seismic characteristics, the Dengying Formation is subdivided into four third-order sequences, with five sequence boundaries and three seismic facies identified. Supported by sequence stratigraphy and geophysical data, we have reconstructed the tectono-sedimentary evolution of the multiple platform margins on the eastern side of the Deyang-Anyue rift in the Sichuan Basin during the late Ediacaran. Our findings indicate that the platform underwent two phases of retrogradation. The second-stage platform margin underwent retrogradation towards the interior, spanning a distance between 10 and 80 km, based on the initial configuration established by the first-stage platform margin. The main controls for progradation and retrogradation of carbonate platforms are eustatic sea-level changes and tectonic activity. Eustatic sea-level changes can be divided into constructive and destructive phases. Constructive phases are commonly observed in highstand systems tracts, while destructive phases are often associated with transgressive systems tracts and are related to platform retrogradation processes. However, sea-level changes alone cannot fully control the process of platform retrogradation. The thermal subsidence following mantle plume events likely played a significant role in the retrogradation of the platform in the study area. During this period, tectonic processes controlled the geometry of the platform and the deposition of carbonates in the platform margin-slope-basin environment. Additionally, karst-related mound-shoal complexes developed extensively along the platform margin of the Dengying Formation in the northwestern Yangtze Craton. The Lower Cambrian dark shales represent high-quality hydrocarbon source rocks, while the Dengying Formation exhibits an optimal source-reservoir configuration.

Abstract The control of potato virus Y (PVY) induced crop failure is a challengeable issue in agricultural chemistry. Although many anti‐PVY agents are designed to focus on the functionally important coat protein (CP) of virus, how these drugs act on CP to inactivate viral pathogenicity, remains largely unknown. Herein, a PVY CP inhibitor ‐3j (S) is disclosed, which is accessed by developing unusually efficient (up to 99% yield) and chemo‐selective (> 99:1 er in most cases) carbene‐catalyzed [3+4] cycloaddition reactions. Compound ‐3j bears a unique arylimidazole‐fused diazepine skeleton and shows chirality‐preferred performance against PVY. In addition, ‐3j (S) as a mediator allows ARG191 (R191) of CP to be identified as a key amino acid site responsible for intercellular movement of virions. R191 is further demonstrated to be critical for the interaction between PVY CP and the plant functional protein NtCPIP, enabling virions to cross plasmodesmata. This key step can be significantly inhibited through bonding with the ‐3j (S) to further impair pathogenic behaviors involving systemic infection and particle assembly. The study reveals the in‐depth mechanism of action of antiviral agents targeting PVY CP, and contributes to new drug structures and synthetic strategies for PVY management.