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- 저자 : Jiapeng Jiao (검색결과 2 건)
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Jihui Yao,Jiapeng Jiao,Ruiqiang Liu,Fei Zha,Xiaojun Guo,Xiaohua Tang,Haifeng Tian,Yue Chang 한국화학공학회 2021 Korean Journal of Chemical Engineering Vol.38 No.7
To improve the dispersion of metals and to enhance the catalytic performance of SAPO-34 molecular sieves, the template-assisted method was applied to synthesize Co, Ni and Zn modified SAPO-34 molecular sieves by using palygorskite as silicon source and tetraethylammonium hydroxide as template. The metal modified SAPO-34 molecular sieves were characterized by XRD, SEM, XPS, N2-adsorption-desorption, NH3-TPD, FTIR, ICP-AES and TG. The N atoms of tetraethylammonium hydroxide exhibited the different forces to three metal ions, thus the acidity of the molecular sieves was further regulated. Compared with metal modified SAPO-34 molecular sieves prepared by impregnation, metal modified SAPO-34 molecular sieves prepared by template-assisted maintained higher surface area, bigger pore volume and better dispersion of metals. The catalytic performance of metal modified SAPO-34 molecular sieves prepared by template-assisted method in the reaction of methanol-to-olefins (MTO) was investigated in the fixed bed reactor. Under the reaction conditions that the reaction temperature was 400 oC, the reaction pressure was 0.1 MPa, the feed WHSV was 2.0 h1 and the mass of catalyst was 0.5 g, Ni modified SAPO-34 molecular sieves exhibited great methanol conversion and high selectivity to light olefins. The selectivity of light olefins reached 95.7%.
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Identification and confirmation of 14-3-3 ζ as a novel target of ginsenosides in brain tissues
Feiyan Chen,Lin Chen,Weifeng Liang,Zhengguang Zhang,Jiao Li,Wan Zheng,Zhu Zhu,Jiapeng Zhu,Yunan Zhao 고려인삼학회 2021 Journal of Ginseng Research Vol.45 No.4
Background: Ginseng can help regulate brain excitability, promote learning and memory, and resist cerebral ischemia in the central nervous system. Ginsenosides are the major effective compounds of Ginseng, but their protein targets in the brain have not been determined. Methods: We screened proteins that interact with the main components of ginseng (ginsenosides) by affinity chromatography and identified the 14-3-3 ζ protein as a potential target of ginsenosides in brain tissues. Results: Biolayer interferometry (BLI) analysis showed that 20(S)-protopanaxadiol (PPD), a ginseng saponin metabolite, exhibited the highest direct interaction to the 14-3-3 ζ protein. Subsequently, BLI kinetics analysis and isothermal titration calorimetry (ITC) assay showed that PPD specifically bound to the 14-3-3 ζ protein. The cocrystal structure of the 14-3-3 ζ protein-PPD complex showed that the main interactions occurred between the residues R56, R127, and Y128 of the 14-3-3 ζ protein and a portion of PPD. Moreover, mutating any of the above residues resulted in a significant decrease of affinity between PPD and the 14-3-3 ζ protein. Conclusion: Our results indicate the 14-3-3 ζ protein is the target of PPD, a ginsenoside metabolite. Crystallographic and mutagenesis studies suggest a direct interaction between PPD and the 14-3-3 ζ protein. This finding can help in the development of small-molecular compounds that bind to the 14-3-3 ζ protein on the basis of the structure of dammarane-type triterpenoid.
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