The rotational parameters estimation of maneuvering target is the key of cross-range scaling of ISAR （inverse synthetic aperture radar）, which can be used in the target feature extraction. The cross-range signal mod...The rotational parameters estimation of maneuvering target is the key of cross-range scaling of ISAR （inverse synthetic aperture radar）, which can be used in the target feature extraction. The cross-range signal model of rotating target with fixed acceleration is presented and the weighted linear least squares estimation of rotational parameters with fixed velocity or acceleration is proposed via the relationship of cross-range FM （frequency modulation） parameter, scatterers coordinates and rotational parameters. The FM parameter is calculated via RWT （Radon-Wigner transform）. The ISAR imaging and cross-range scaling based on scaled RWT imaging method are implemented after obtaining rotational parameters. The rotational parameters estimation and cross-range scaling are validated by the ISAR processing of experimental radar data, and the method presents good application foreground to the ISAR imaging and scaling of maneuvering target.展开更多
In order to produce millimeter-scale plasmas for the research of laser-plasma interactions （LPIs）, gasbag target is designed and tested on Shenguang-III prototype laser facility. The x-ray pinhole images show that m...In order to produce millimeter-scale plasmas for the research of laser-plasma interactions （LPIs）, gasbag target is designed and tested on Shenguang-III prototype laser facility. The x-ray pinhole images show that millimeter-scale plasmas are produced with the gasbag. The electron temperature inferred from the stimulated Raman scattering （SRS） spectrum is about 1.6 keV. The SRS spectrum also indicates that the electron density has a fiat region within the duration of 200 ps. The obvious differences between the results of the gasbag and that of the void half hohlraum show the feasibility of the gasbag target in creating millimeter-scale plasmas. The LPIs in these millimeter-scale plasmas may partially mimic those in the ignition condition because the duration of the existence of a flat plasma density is much larger than the growth time of the two main instabilities, i.e., SRS and stimulated Brillouin scattering （SBS）. So we make the conclusion that the gasbag target can be used to research the large-scale LPIs.展开更多
Background:Human immunodeficiency virus type 1(HIV-1)remains a persistent global health challenge.Therefore,a continuous exploration of novel therapeutic strategies is essential.A comprehensive understanding of how HI...Background:Human immunodeficiency virus type 1(HIV-1)remains a persistent global health challenge.Therefore,a continuous exploration of novel therapeutic strategies is essential.A comprehensive understanding of how HIV-1 utilizes the cellular metabolism machinery for replication can provide insights into new therapeutic approaches.Methods:In this study,we performed a flux balance analysis using a genome-scale metabolic model(GEM)integrated with an HIV-1 viral biomass objective function to identify potential targets for anti–HIV-1 interventions.We generated a GEM by integrating an HIV-1 production reaction into CD4+T cells and optimized for both host and virus optimal states as objective functions to depict metabolic profiles of cells in the status for optimal host biomass maintenance or for optimal HIV-1 virion production.Differential analysis was used to predict biochemical reactions altered optimal for HIV-1 production.In addition,we conducted in silico simulations involving gene and reaction knock-outs to identify potential anti–HIV-1 targets,which were subsequently validated by human phytohemagglutinin(PHA)blasts infected with HIV-1.Results:Differential analysis identified several altered biochemical reactions,including increased lysine uptake and oxidative phosphorylation(OXPHOS)activities in the virus optima compared with the host optima.In silico gene and reaction knock-out simulations revealed de novo pyrimidine synthesis,and OXPHOS could serve as potential anti–HIV-1 metabolic targets.In vitro assay confirmed that targeting OXPHOS using metformin could suppress the replication of HIV-1 by 56.6%(385.4±67.5 pg/mL in the metformintreated group vs.888.4±32.3 pg/mL in the control group,P<0.001).Conclusion:Our integrated host-virus genome-scale metabolic study provides insights on potential targets(OXPHOS)for anti-HIV therapies.展开更多
基金supported by the National Natural Science Foundation of China (60875019)
文摘The rotational parameters estimation of maneuvering target is the key of cross-range scaling of ISAR （inverse synthetic aperture radar）, which can be used in the target feature extraction. The cross-range signal model of rotating target with fixed acceleration is presented and the weighted linear least squares estimation of rotational parameters with fixed velocity or acceleration is proposed via the relationship of cross-range FM （frequency modulation） parameter, scatterers coordinates and rotational parameters. The FM parameter is calculated via RWT （Radon-Wigner transform）. The ISAR imaging and cross-range scaling based on scaled RWT imaging method are implemented after obtaining rotational parameters. The rotational parameters estimation and cross-range scaling are validated by the ISAR processing of experimental radar data, and the method presents good application foreground to the ISAR imaging and scaling of maneuvering target.
基金Project supported by the National Natural Science Foundation of China (Grant No. 10625523)the Innovation Project of the Chinese Academy of Sciences (Grant No. KJCX2-YW-N36)National High-Tech Program of China
文摘In order to produce millimeter-scale plasmas for the research of laser-plasma interactions （LPIs）, gasbag target is designed and tested on Shenguang-III prototype laser facility. The x-ray pinhole images show that millimeter-scale plasmas are produced with the gasbag. The electron temperature inferred from the stimulated Raman scattering （SRS） spectrum is about 1.6 keV. The SRS spectrum also indicates that the electron density has a fiat region within the duration of 200 ps. The obvious differences between the results of the gasbag and that of the void half hohlraum show the feasibility of the gasbag target in creating millimeter-scale plasmas. The LPIs in these millimeter-scale plasmas may partially mimic those in the ignition condition because the duration of the existence of a flat plasma density is much larger than the growth time of the two main instabilities, i.e., SRS and stimulated Brillouin scattering （SBS）. So we make the conclusion that the gasbag target can be used to research the large-scale LPIs.
基金the National Natural Science Foundation of China(82071784)the Fundamental Research Funds for the Central Universities(2042022dx0003 and PTPP2023002)+1 种基金the Key Research and Development Project of Hubei Province(2020BCA069)the Translational Medicine and Interdisciplinary Research Joint Fund of Zhongnan Hospital of Wuhan University(ZNJC202007).
文摘Background:Human immunodeficiency virus type 1(HIV-1)remains a persistent global health challenge.Therefore,a continuous exploration of novel therapeutic strategies is essential.A comprehensive understanding of how HIV-1 utilizes the cellular metabolism machinery for replication can provide insights into new therapeutic approaches.Methods:In this study,we performed a flux balance analysis using a genome-scale metabolic model(GEM)integrated with an HIV-1 viral biomass objective function to identify potential targets for anti–HIV-1 interventions.We generated a GEM by integrating an HIV-1 production reaction into CD4+T cells and optimized for both host and virus optimal states as objective functions to depict metabolic profiles of cells in the status for optimal host biomass maintenance or for optimal HIV-1 virion production.Differential analysis was used to predict biochemical reactions altered optimal for HIV-1 production.In addition,we conducted in silico simulations involving gene and reaction knock-outs to identify potential anti–HIV-1 targets,which were subsequently validated by human phytohemagglutinin(PHA)blasts infected with HIV-1.Results:Differential analysis identified several altered biochemical reactions,including increased lysine uptake and oxidative phosphorylation(OXPHOS)activities in the virus optima compared with the host optima.In silico gene and reaction knock-out simulations revealed de novo pyrimidine synthesis,and OXPHOS could serve as potential anti–HIV-1 metabolic targets.In vitro assay confirmed that targeting OXPHOS using metformin could suppress the replication of HIV-1 by 56.6%(385.4±67.5 pg/mL in the metformintreated group vs.888.4±32.3 pg/mL in the control group,P<0.001).Conclusion:Our integrated host-virus genome-scale metabolic study provides insights on potential targets(OXPHOS)for anti-HIV therapies.
