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低蛋白日粮中添加亮氨酸通过雷帕霉素靶蛋白信号通路增加成年大鼠骨骼肌重量及蛋白质合成
张博, 楚丽翠, 刘宏, 谢春元, 谯仕彦, 曾祥芳
《工程(英文)》 2017年 第3卷 第5期 页码 760-765 doi: 10.1016/J.ENG.2017.03.008
低蛋白日粮会减少动物组织中蛋白质沉积,影响骨骼肌增重。本文旨在研究低蛋白日粮中添加亮氨酸对成年大鼠骨骼肌重量和蛋白质合成的影响。试验第11天,所有大鼠大剂量一次性腹腔注射L-[ring-2H5]苯丙氨酸注射液,测定血清中的氨基酸含量、比目鱼肌和腓肠肌重量、蛋白质合成速率及mTOR信号通路相关分子的表达。结果表明,在3个处理中,RL组血清亮氨酸含量最高(P < 0.05),而异亮氨酸含量最低(P < 0.05);CON组的缬氨酸含量低于R和RL组(P < 0.05),但采食量、蛋白质合成速度和与R组相比,RL组可以增加腓肠肌重量(P < 0.05),促进S6K1磷酸化(P < 0.05),增加骨骼肌蛋白质合成(P < 0.05)。本文结论如下,在成年大鼠长期采食低蛋白日粮的情况下,日粮中添加亮氨酸可以改善大鼠的生长性能,通过提高mTOR通路中S6K1磷酸化水平,促进大鼠骨骼肌蛋白质合成,抑制蛋白质降解。
时间序列多组学整合分析揭示原代肝细胞体外培养去分化过程伴随非降解性泛素化修饰的增加 Article
姜正一, 孙泽宇, 欧阳晓希, 赵亚磊, 周梦豪, 王保红, 李启睿, 范林骁, 张赛男, 李兰娟
《工程(英文)》 2020年 第6卷 第11期 页码 1302-1314 doi: 10.1016/j.eng.2020.02.011
人类蛋白质N-糖基化的十二年全基因组关联研究 Review
Anna Timoshchuk, Sodbo Sharapov, Yurii S. Aulchenko
《工程(英文)》 2023年 第26卷 第7期 页码 17-31 doi: 10.1016/j.eng.2023.03.013
Most human-secreted and membrane-bound proteins have covalently attached oligosaccharide chains, or glycans. Glycosylation influences the physical and chemical properties of proteins, as well as their biological functions. Unsurprisingly, alterations in protein glycosylation have been implicated in a growing number of human diseases, and glycans are increasingly being considered as potential therapeutic targets, an essential part of therapeutics, and biomarkers. Although glycosylation pathways are biochemically well-studied, little is known about the networks of genes that guide the cell- and tissue-specific regulation of these biochemical reactions in humans in vivo. The lack of a detailed understanding of the mechanisms regulating glycome variation and linking the glycome to human health and disease is slowing progress in clinical applications of human glycobiology. Two of the tools that can provide much sought-after knowledge of human in vivo glycobiology are human genetics and genomics, which offer a powerful data-driven agnostic approach for dissecting the biology of complex traits. This review summarizes the current state of human populational glycogenomics. In Section 1, we provide a brief overview of the N-glycan's structural organization, and in Section 2, we give a description of the major blood plasma glycoproteins. Next, in Section 3, we summarize, systemize, and generalize the results from current N-glycosylation genome-wide association studies (GWASs) that provide novel knowledge of the genetic regulation of the populational variation of glycosylation. Until now, such studies have been limited to an analysis of the human blood plasma N-glycome and the N-glycosylation of immunoglobulin G and transferrin. While these three glycomes make up a rather limited set compared with the enormous multitude of glycomes of different tissues and glycoproteins, the study of these three does allow for powerful analysis and generalization. Finally, in Section 4, we turn to genes in the established loci, paying particular attention to genes with strong support in Section 5. At the end of the review, in Sections 6 and 7, we describe special cases of interest in light of new discoveries, focusing on possible mechanisms of action and biological targets of genetic variation that have been implicated in human protein N-glycosylation.
转录因子HNF1A、HNF4A和FOXA2调节肝细胞蛋白质N-糖基化 Article
Vedrana Vičić Bočkor,Nika Foglar,Goran Josipović,Marija Klasić,Ana Vujić,Branimir Plavša,Toma Keser,Samira Smajlović,Aleksandar Vojta,Vlatka Zoldoš
《工程(英文)》 2024年 第32卷 第1期 页码 58-69 doi: 10.1016/j.eng.2023.09.019
Hepatocyte nuclear factor 1 alpha (HNF1A), hepatocyte nuclear factor 4 alpha (HNF4A), and forkhead box protein A2 (FOXA2) are key transcription factors that regulate a complex gene network in the liver, creating a regulatory transcriptional loop. The Encode and ChIP-Atlas databases identify the recognition sites of these transcription factors in many glycosyltransferase genes. Our in silico analysis of HNF1A, HNF4A, and FOXA2 binding to the 10 candidate glyco-genes studied in this work confirms a significant enrichment of these transcription factors specifically in the liver. Our previous studies identified HNF1A as a master regulator of fucosylation, glycan branching, and galactosylation of plasma glycoproteins. Here, we aimed to functionally validate the role of the three transcription factors on downstream glyco-gene transcriptional expression and the possible effect on glycan phenotype. We used the state-of-the-art clustered regularly interspaced short palindromic repeats/dead Cas9 (CRISPR/dCas9) molecular tool for the downregulation of the HNF1A, HNF4A, and FOXA2 genes in HepG2 cells—a human liver cancer cell line. The results show that the downregulation of all three genes individually and in pairs affects the transcriptional activity of many glyco-genes, although downregulation of glyco-genes was not always followed by an unambiguous change in the corresponding glycan structures. The effect is better seen as an overall change in the total HepG2 N-glycome, primarily due to the extension of biantennary glycans. We propose an alternative way to evaluate the N-glycome composition via estimating the overall complexity of the glycome by quantifying the number of monomers in each glycan structure. We also propose a model showing feedback loops with the mutual activation of HNF1A–FOXA2 and HNF4A–FOXA2 affecting glyco-genes and protein glycosylation in HepG2 cells.
关键词: Clustered regularly interspaced short palindromic repeats/dead Cas9 (CRISPR/dCas9) Epigenetics Hepatocyte nuclear factor 1 alpha (HNF1A) Hepatocyte nuclear factor 4 alpha (HNF4A) Forkhead box protein A2 (FOXA2) N-glycosylation HepG2 cells
李荣和,姜浩奎
《中国工程科学》 2003年 第5卷 第3期 页码 72-74
采用大豆功效成份连续提取、逆向留存大豆蛋白技术,生产新型大豆浓缩蛋白(纯度≥70%)可将大豆浓缩蛋白成本降至<0.22万元/t,是国内外同类产品成本的1/3,在面粉中添加5%~8%新型大豆浓缩蛋白,可使面制主食中大豆蛋白含量提高3.5%~5.6%,而且可全面改善面制主食的品质,不增加面粉与面制主食的售价。
中东呼吸综合征病毒(MERS-CoV)蛋白的分子特征、功能及其致病性 Review
李艳华, 胡晨雨, 吴南屏, 姚航平, 李兰娟
《工程(英文)》 2019年 第5卷 第5期 页码 940-947 doi: 10.1016/j.eng.2018.11.035
靶向膜蛋白的抗体药物开发的新进展 Review
Georgina To’a Salazar, 黄子逸, 张凝艳, 张学光, 安志强
《工程(英文)》 2021年 第7卷 第11期 页码 1541-1551 doi: 10.1016/j.eng.2020.11.013
在疾病干预的众多膜蛋白靶标中,G蛋白偶联受体(GPCR)作为人体内最大的膜受体蛋白家族,成为很多药物的重要靶点,其次是离子通道、转运蛋白和激酶等膜蛋白在细胞信号转导和运输中发挥了关键作用,当前药物研发面临的挑战在于进一步发掘此类膜蛋白的潜在靶点的干预价值,开发治疗性抗体药物。鉴于特异性抗体能够识别膜蛋白的灵敏特性,以及随着基因工程技术的进步,对已有抗体进行加工改造可获得适应多个靶点蛋白的特异性抗体。然而,成功分离特异靶向膜蛋白抗体取决于一系列因素。我们更易研制和识别结构简单且具有长片段胞外区的抗体分子,但对于高难度的靶点蛋白,如GPCR和其他复杂膜蛋白往往难以得到具有活性的候选抗体。深入研究靶标膜蛋白的结构有助于推进治疗性抗体药物的开发进程。本文概述了抗体靶向复杂膜蛋白的优势和挑战,以及膜蛋白抗原制备和抗体研发策略的最新进展。
浦华 ,杨静 ,王永伟 ,涂涛 ,李燕松 ,罗会颖 ,姚斌
《中国工程科学》 2023年 第25卷 第4期 页码 149-157 doi: 10.15302/J-SSCAE-2023.04.003
针对于此,本文梳理蛋白饲料资源基本情况、分析饲料蛋白替代潜力、提出蛋白替代战略构想,以期为增强蛋白饲料资源的有效供给提供借鉴。蛋白资源传统加工技术存在短板
目前我国的蛋白资源多采用传统加工工艺获取,存在消化利用率低、蛋白质含量变异大、氨基酸组成不理想、含有内源毒素和抗营养因子等限制因素。例如,菜粕蒸炒温度较高、时间较长,导致蛋白质和氨基酸破坏严重,饼粕价值降低。② 谷物及加工副产物类饲料资源开发利用水平总体不高。
关键词: 粮食安全;蛋白饲料资源;蛋白替代;豆粕
新型冠状病毒HCoV-19 S蛋白与人ACE2蛋白表面糖链和独特翻译后修饰的质谱分析 Article
孙泽宇, 任科燚, 张兴, 陈景华, 姜正一, 江静, 季飞洋, 欧阳晓希, 李兰娟
《工程(英文)》 2021年 第7卷 第10期 页码 1441-1451 doi: 10.1016/j.eng.2020.07.014
基于微流控工程的高强力学性能蛋白纤维 Review
孙静, 陈静思, 刘凯, 曾洪波
《工程(英文)》 2021年 第7卷 第5期 页码 615-623 doi: 10.1016/j.eng.2021.02.005
普列克底物蛋白同源物样结构域家族A成员1蛋白——导致代谢疾病的多方面细胞存活因素 Review
Tamana Yousof, Jae Hyun Byun, Jack Chen, Richard C. Austin
《工程(英文)》 2023年 第20卷 第1期 页码 9-18 doi: 10.1016/j.eng.2022.05.014
普列克底物蛋白同源物样结构域家族A成员1(PHLDA1)是多作用的胞内蛋白,属于进化上保守的普列克底物蛋白同源相关结构域家族。本文综述了PHLDA1基因及蛋白调控、定位和功能方面的现有知识。本文重点介绍了PHLDA1促凋亡和抗凋亡,进而导致代谢性疾病的作用。
糖尿病发作后心脏脂蛋白脂肪酶的变化 Review
Chae Syng Lee, Yajie Zhai, Brian Rodrigues
《工程(英文)》 2023年 第20卷 第1期 页码 19-25 doi: 10.1016/j.eng.2022.06.013
标题 作者 时间 类型 操作
转录因子HNF1A、HNF4A和FOXA2调节肝细胞蛋白质N-糖基化
Vedrana Vičić Bočkor,Nika Foglar,Goran Josipović,Marija Klasić,Ana Vujić,Branimir Plavša,Toma Keser,Samira Smajlović,Aleksandar Vojta,Vlatka Zoldoš
期刊论文
普列克底物蛋白同源物样结构域家族A成员1蛋白——导致代谢疾病的多方面细胞存活因素
Tamana Yousof, Jae Hyun Byun, Jack Chen, Richard C. Austin
期刊论文