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Aggregate 2024年第1期5卷 167-174页

作者： Hang Gao Shen-Yu Shi shu-minwang Qian-Qian Tao Hui-Li Ma Jun Hu Hong-Yuan Chen Jing-Juan Xu State Key Laboratory of Analytical Chemistry for Life Science School of Chemistry and Chemical EngineeringNanjing UniversityNanjingChina Key Laboratory of Flexible Electronics(KLOFE)and Institute of Advanced Materials(IAM) Nanjing Tech UniversityNanjingChina School of Life Science and Health Engineering Jiangnan UniversityWuxiChina

Full utilization of the excited species at both singlet states(1R*)and triplet states(3R*)is crucial to improving electrochemiluminescence(ECL)efficiency but is challenging for organic luminescent ***,an aggregation-induced delayed ECL(AIDECL)active organic dot(OD)containing a benzophenone acceptor and dimethylacridine donor is reported,which shows high ECL efficiency via reverse intersystem crossing(RISC)of non-emissive 3R*to emissive 1R*,overcoming the spin-forbidden radiative decay from 3R*.By introducing dual donor-acceptor pairs into luminophores,it is found that nonradiative pathway could be further suppressed via enhanced intermolecular weak interactions,and multiple spin-up conversion channels could be *** a consequence,the obtained OD enjoys a 6.8-fold higher ECL efficiency relative to the control AIDECL-active ***-crystal studies and theoretical calculations reveal that the enhanced AIDECL behaviors come from the acceleration of both radiative transition and *** work represents a major step towards purely organic,high-efficiency ECL dyes and a direction for the design of next-generation ECL dyes at the molecular level.

关键词： aggregation-induced delayed electrochemiluminescence benzophenone dimethylacridine organic dots reverse intersystem crossing

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Expression of hepatitis B virus X protein in transgenic mice

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World Journal of Gastroenterology 2003年第1期9卷 112-116页

作者： JunXiong Yu-ChengYao Xiao-YuanZi Jian-XiuLi Xin-minwang Xu-TingYe shu-MinZhao Yong-BiYan Hong-YuYu Yi-PingHu DepartmentofCellBiology SecondMilitary'MedicalUniversity-Shanghai200433.China DepartmentofPathology.ChangzhengHospital SecondMilitaUMedicalUniversityShanghai200433China DepartmentofCellBiology SecondMilitary'MedicalUniversity-Shanghai200433.China

AIM: To establish a mice model harboring hepatitis B virusx gene (adr subtype) for studying the function of hepatitis Bvirus X protein, a transactivator of viral and cellular promoter/enhancer ***: Expression vector pcDNA3-HBx, containing CMVpromoter and hepatitis B virus x gene open reading fragment,was constructed by recombination DNA technique. Hela cellswere cultured in DMEM and transfected with pcDNA3-HBxor control pcDNA3 plasmids using FuGENE6 TransfectionReagent. Expression of pcDNA3-HBx vectors in thetransfected Hela cells was confirmed by Western *** restriction endonudease digestion, the coding elementswere microinjected into male pronuclei of mice zygotes. Thepups were evaluated by multiplex polymerase chain reaction(PCR) at genomic DNA level. The x gene transgenic micefounders were confirmed at protein level by Western blotting,immunohistochemistry and immunogold transmissionelectron ***: Expression vector pcDNA3-HBxwas constructedby recombination DNA technique and identified right byrestriction endonuclease digestion and DNA directsequencing. With Western blotting, hepatitis X protein wasdetected in Hela cells transfected with pcDNA3-HBxplasmids,suggesting pcDNA3-HBxplasmids could express in eukaryoticcells. Following microinjection of coding sequence ofpcDNA3-HBx, the embryos were transferred to oviducts ofpsedopregnant females. Four pups were born and *** of them were verified to have the HBxgene integratedin their genomic DNA by multiplex PCR assay, and namedC57-TgN(HBx)SMMU1 and C57-TgN(HBx)SMMU3respectively. They expressed 17KD X protein in liver tissueby Western blotting assay. With the immunohistochemistry,X protein was detected mainly in hepatocytes cytoplasm oftransgenic mice, which was furthermore confirmed byimmunogold transmission electon ***: We have constructed the expression vectorpcDNA3-HBxthat can be used to study the function of HBxgene in eukaryotic cellsin vitro. We al

关键词：乙肝病毒X蛋白转基因技术动物模型 DNA重组技术慢性乙型肝炎

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