1.The clinical reseach of early enteral nutrition through jejunostomy after total gastrectomy
Wenrui JIANG ; Zimiao HU ; Ming CHANG ;
Parenteral & Enteral Nutrition 1997;0(03):-
Objectives:To investigate the effect of early enteral nutrition after total gastrectomy and evaluate its feasibility. Methods:25 cases of postoprative patients of stomacch carcinoma after total gastrectomy were selected and is divided into two groups at random.12 cases (control group) had accepted parenteral nutrition after operation.13 cases(test group) had accepted enteral nutrition after 24 hours of the operation though jejunostomy.The study continued for 7 days. The energy was equal approximately between groups.The nutrition state was evaluated in two groups before and after operation,and the recovery of intestinal function and hospitalized charge were compared too. Results:The postoperative body weight and nutrition state in the test group were better than those in control group and the differnces were very significant( P
3.Structure of the catalytic domain of a state transition kinase homolog from Micromonas algae.
Jiangtao GUO ; Xuepeng WEI ; Mei LI ; Xiaowei PAN ; Wenrui CHANG ; Zhenfeng LIU
Protein & Cell 2013;4(8):607-619
Under natural environments, plants and algae have evolved various photosynthetic acclimation mechanisms in response to the constantly changing light conditions. The state transition and long-term response processes in photosynthetic acclimation involve remodeling and composition alteration of thylakoid membrane. A chloroplast protein kinase named Stt7/STN7 has been found to have pivotal roles in both state transition and long-term response. Here we report the crystal structures of the kinase domain of a putative Stt7/STN7 homolog from Micromonas sp. RCC299 (MsStt7d) in the apo form and in complex with various nucleotide substrates. MsStt7d adopts a canonical protein kinase fold and contains all the essential residues at the active site. A novel hairpin motif, found to be a conserved feature of the Stt7/STN7 family and indispensable for the kinase stability, interacts with the activation loop and fixes it in an active conformation. We have also demonstrated that MsStt7d is a dualspecifi city kinase that phosphorylates both Thr and Tyr residues. Moreover, preliminary in vitro data suggest that it might be capable of phosphorylating a consensus N-terminal pentapeptide of light-harvesting proteins Micromonas Lhcp4 and Arabidopsis Lhcb1 directly. The potential peptide/protein substrate binding site is predicted based on the location of a pseudo-substrate contributed by the adjacent molecule within the crystallographic dimer. The structural and biochemical data presented here provide a framework for an improved understanding on the role of Stt7/STN7 in photosynthetic acclimation.
Amino Acid Sequence
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Amino Acid Substitution
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Arabidopsis
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metabolism
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Arabidopsis Proteins
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chemistry
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genetics
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metabolism
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Binding Sites
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Catalytic Domain
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Chlorophyta
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enzymology
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Crystallography, X-Ray
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Cyclin-Dependent Kinase 2
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chemistry
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metabolism
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Molecular Sequence Data
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Phosphorylation
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Protein Structure, Secondary
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Protein-Serine-Threonine Kinases
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chemistry
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genetics
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metabolism
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Sequence Alignment
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Substrate Specificity
4.Structural insights into the catalytic mechanism of aldehyde-deformylating oxygenases.
Chenjun JIA ; Mei LI ; Jianjun LI ; Jingjing ZHANG ; Hongmei ZHANG ; Peng CAO ; Xiaowei PAN ; Xuefeng LU ; Wenrui CHANG
Protein & Cell 2015;6(1):55-67
The fatty alk(a/e)ne biosynthesis pathway found in cyanobacteria gained tremendous attention in recent years as a promising alternative approach for biofuel production. Cyanobacterial aldehyde-deformylating oxygenase (cADO), which catalyzes the conversion of Cn fatty aldehyde to its corresponding Cn-1 alk(a/e)ne, is a key enzyme in that pathway. Due to its low activity, alk(a/e)ne production by cADO is an inefficient process. Previous biochemical and structural investigations of cADO have provided some information on its catalytic reaction. However, the details of its catalytic processes remain unclear. Here we report five crystal structures of cADO from the Synechococcus elongates strain PCC7942 in both its iron-free and iron-bound forms, representing different states during its catalytic process. Structural comparisons and functional enzyme assays indicate that Glu144, one of the iron-coordinating residues, plays a vital role in the catalytic reaction of cADO. Moreover, the helix where Glu144 resides exhibits two distinct conformations that correlates with the different binding states of the di-iron center in cADO structures. Therefore, our results provide a structural explanation for the highly labile feature of cADO di-iron center, which we proposed to be related to its low enzymatic activity. On the basis of our structural and biochemical data, a possible catalytic process of cADO was proposed, which could aid the design of cADO with improved activity.
Aldehyde Oxidoreductases
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chemistry
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genetics
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metabolism
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Amino Acid Sequence
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Amino Acid Substitution
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Bacterial Proteins
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chemistry
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genetics
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metabolism
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Binding Sites
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Biocatalysis
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Crystallography, X-Ray
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Gas Chromatography-Mass Spectrometry
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Ligands
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Molecular Dynamics Simulation
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Molecular Sequence Data
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Protein Structure, Tertiary
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Sequence Alignment
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Synechococcus
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enzymology
5.Efficacy and safety of eltrombopag in aplastic anemia: A multi-center survey in China
Wenrui YANG ; Bing HAN ; Hong CHANG ; Bingyi WU ; Fankai MENG ; Dexiang JI ; Yingmei LI ; Zhengjin ZHENG ; Yan FEI ; Jianping SHEN ; Ping HU ; Xiaoqing DING ; Peng ZHANG ; Yongqing WANG ; Fengkui ZHANG
Chinese Journal of Hematology 2020;41(11):890-895
Objective:To evaluate the safety and efficacy of eltrombopag combined with immunosuppressive therapy in patients with aplastic anemia (AA) in China.Methods:We investigated and analyzed the clinical data of AA patients from 14 hematological treatment centers who were treated with oral eltrombopag for at least 3 mon.Results:We enrolled 56 AA patients, including 19 treatment-na?ve patients and 37 IST-refractory patients. The median administration period for eltrombopag was 7 (3-31) months, and the median maximum stable dosage was 75 mg/d (50-150 mg/d) . The 3-month hematological response (HR) rate was 60%, and the complete response (CR) rate was 30% in 10 SAA patients who were treated with first-line eltrombopag and standard IST (ATG+CsA) . Eight of 9 eltrombopag and CsA ± androgen first-line treated SAA patients responded (8/9, 89%) and 4 (44%) gave CR. The overall HR and CR rates were 79% and 52.6%, respectively, among these 19 patients by the end of the follow-up period. Of the 19 AA patients who were refractory to CsA ± androgen, 11 achieved HR (57.9%) at 3 mon, and the best HR rate was 44% in standard IST (ATG+CsA) refractory 18 patients after eltrombopag treatment. Fifty-one percent of the patients experienced mild or moderate adverse events, and gastrointestinal discomfort was the most common adverse effect reported by the study subjects.Conclusion:Adding Eltrombopag in first-line IST can accelerate the acquisition and improve the quality of hematological responses in AA patients. AA with relatively more residual hematopoietic cells may be well treated with eltrombopag and non-ATG IST. Eltrombopag can be used as salvage therapy for CsA±androgen refractory patients. Eltrombopag was generally safe and well tolerated by AA patients in China.