Microscale crystallization is at the frontier of chemical engineering,material science,and biochemical research and is affected by many factors.The precise regulation and control of microscale crystal processes is sti...Microscale crystallization is at the frontier of chemical engineering,material science,and biochemical research and is affected by many factors.The precise regulation and control of microscale crystal processes is still a major challenge.In the heterogeneous induced nucleation process,the chemical and micro/nanostructural characteristics of the interface play a dominant role.Ideal crystal products can be obtained by modifying the interface characteristics,which has been proven to be a promising strategy.This review illustrates the application of interface properties,including chemical characteristics(hydropho-bicity and functional groups)and the morphology of micro/nanostructures(rough structure and cavities,pore shape and pore size,surface porosity,channels),in various microscale crystallization controls and process intensification.Finally,possible future research and development directions are outlined to emphasize the importance of interfacial crystallization control and regulation for crystal engineering.展开更多
Kidney disease has become a global public health problem affecting over 750 million people worldwide and imposing a heavy economic burden on patients.The complex architecture of the human kidney makes it very difficul...Kidney disease has become a global public health problem affecting over 750 million people worldwide and imposing a heavy economic burden on patients.The complex architecture of the human kidney makes it very difficult to study the pathophysiology of renal diseases in vitro and to develop effective therapeutic options for patients.Even though cell lines and animal models have enriched our understanding,they fail to recapitulate key aspects of human kidney development and renal disease at cellular and functional levels.Organoids can be derived from either pluripotent stem cells or adult stem cells by strictly regulating key signalling pathways.Today,these self-differentiated organoids represent a promising technology to further understand the human kidney,one of the most complex organs,in an unprecedented way.The newly established protocols improved by organ-on-chip and coculture with immune cells will push kidney organoids towards the next generation.Herein,we focus on recent achievements in the application of kidney organoids in disease modelling,nephrotoxic testing,precision medicine,biobanking,and regenerative therapy,followed by discussions of novel strategies to improve their utility for biomedical research.The applications we discuss may help to provide new ideas in clinical fields.展开更多
Thirty-one new 10,12-disubstituted aloperine derivatives were subtly constructed through a selective oxidation on the 10-α-C-H induced by sulfonyl and a nucleophilic substitution with the stereoselectivity and scalab...Thirty-one new 10,12-disubstituted aloperine derivatives were subtly constructed through a selective oxidation on the 10-α-C-H induced by sulfonyl and a nucleophilic substitution with the stereoselectivity and scalability.Of them,compound 6b displayed a moderate anti-human coronavirus OC43(HCoV-OC43)potency and blocked the viral entry stage through a host mechanism of action.Using chemoproteomic techniques,both transmembrane serine protease 2(TMPRSS2)and scavenger receptor class B type 1(SR-B1)proteins,which act as host cofactors of viral entry,were identified to be the direct targets of 6b against HCoV-OC43.Furthermore,6b may deactivate the TMPRSS2 by inducing a change in protein conformation,rather than binding to its catalytic center,thus suppressing the viral membrane fusion.Accordingly,our study provided key scientific data for the development of aloperine derivatives into a new class of antiviral candidates against humanβ-coronavirus,including severe acute respiratory syndrome coronavirus 2(SARS-CoV-2).展开更多
基金Creative Research Groups of the National Natural Science Foundation of China(Grant No.22021005)National Natural Science Foundation of China(Grant Nos.21978037 and 21978033)+3 种基金Fundamental Research Funds for the Central Universities(Grant No.DUT19TD33)National Key Research and Development Program of China(Grant No.2019YFE0119200)Support Plan of Innovative Talents of Liaoning Province(Grant Nos.XLYC1901005,XLYC1907149,XLYC1907063)Dalian Innovative Science and Technology Fund(Grant Nos.2020JJ26SN064 and 2021JJ12GX019).
文摘Microscale crystallization is at the frontier of chemical engineering,material science,and biochemical research and is affected by many factors.The precise regulation and control of microscale crystal processes is still a major challenge.In the heterogeneous induced nucleation process,the chemical and micro/nanostructural characteristics of the interface play a dominant role.Ideal crystal products can be obtained by modifying the interface characteristics,which has been proven to be a promising strategy.This review illustrates the application of interface properties,including chemical characteristics(hydropho-bicity and functional groups)and the morphology of micro/nanostructures(rough structure and cavities,pore shape and pore size,surface porosity,channels),in various microscale crystallization controls and process intensification.Finally,possible future research and development directions are outlined to emphasize the importance of interfacial crystallization control and regulation for crystal engineering.
基金This study was supported by grants from Undergraduate Inno-vation and Entrepreneurship Project(No.202321007)Hunan Innovative Provincial Construction Project(No.20195K2211)+7 种基金Changsha Science,Technology Plan Project(No.kq2001044)the National Natural Science Foundation of China(No.81970248)National Key Research and Development Program of China(No.2018YFA0108700,2017YFA0105602)NSFC Pro-jects of Intemational Cooperation and Exchanges(No.81720108004)National Natural Science Foundation of China(No.81974019)The Research Team Project of Natural Science Foundation of Guangdong Province of China(No.2017A030312007)The Key Program of Guangzhou Science Research Plan(No.201904020047)The Special Project of Dengfeng Program of Guangdong Provincial People's Hospital(No.DFJH201812,KJ012019119,KJ012019423).
文摘Kidney disease has become a global public health problem affecting over 750 million people worldwide and imposing a heavy economic burden on patients.The complex architecture of the human kidney makes it very difficult to study the pathophysiology of renal diseases in vitro and to develop effective therapeutic options for patients.Even though cell lines and animal models have enriched our understanding,they fail to recapitulate key aspects of human kidney development and renal disease at cellular and functional levels.Organoids can be derived from either pluripotent stem cells or adult stem cells by strictly regulating key signalling pathways.Today,these self-differentiated organoids represent a promising technology to further understand the human kidney,one of the most complex organs,in an unprecedented way.The newly established protocols improved by organ-on-chip and coculture with immune cells will push kidney organoids towards the next generation.Herein,we focus on recent achievements in the application of kidney organoids in disease modelling,nephrotoxic testing,precision medicine,biobanking,and regenerative therapy,followed by discussions of novel strategies to improve their utility for biomedical research.The applications we discuss may help to provide new ideas in clinical fields.
基金supported by the National Natural Science Foundation of China(No.81974494)CAMS Innovation Fund for Medical Sciences(No.2021-I2M-1-070).
文摘Thirty-one new 10,12-disubstituted aloperine derivatives were subtly constructed through a selective oxidation on the 10-α-C-H induced by sulfonyl and a nucleophilic substitution with the stereoselectivity and scalability.Of them,compound 6b displayed a moderate anti-human coronavirus OC43(HCoV-OC43)potency and blocked the viral entry stage through a host mechanism of action.Using chemoproteomic techniques,both transmembrane serine protease 2(TMPRSS2)and scavenger receptor class B type 1(SR-B1)proteins,which act as host cofactors of viral entry,were identified to be the direct targets of 6b against HCoV-OC43.Furthermore,6b may deactivate the TMPRSS2 by inducing a change in protein conformation,rather than binding to its catalytic center,thus suppressing the viral membrane fusion.Accordingly,our study provided key scientific data for the development of aloperine derivatives into a new class of antiviral candidates against humanβ-coronavirus,including severe acute respiratory syndrome coronavirus 2(SARS-CoV-2).