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Cellular and Molecular Basis of Leptin Resistance in Obese Patients
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作者 Xiao-ting Ma Shao-qin Ge 《Food Therapy and Health Care》 2020年第3期122-128,共7页
Obesity is a major risk factor for diabetes,cardiovascular disease,and certain cancers.It arises from a chronic positive energy balance.This is usually due to unrestricted access to food in the context of genetic and ... Obesity is a major risk factor for diabetes,cardiovascular disease,and certain cancers.It arises from a chronic positive energy balance.This is usually due to unrestricted access to food in the context of genetic and epigenetic vulnerabilities.And an increasingly sedentary lifestyle.Over the past few decades,our understanding of the fluid and nervous systems that mediate energy balance control has greatly improved.However,our ability to formulate effective strategies to slow the current obesity epidemic has been hampered,mainly because we have limited knowledge of the resistance mechanisms of metabolic hormones such as leptin.Resistance to leptin is a sign of obesity,leptin is a key hormone for neuroendocrine control of energy balance.In the past few years,we have made tremendous progress in our in-depth research on the cellular pathways that disrupt the action of leptin.In this review,we discuss the molecular mechanisms of leptin resistance and how to use them as targets for obesity drug therapy. 展开更多
关键词 OBESITY LEPTIN Leptin resistance Cellular basis molecular basis
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Molecular Basis of Transfer of Induced Resistance in Plants
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作者 徐文联 董汉松 +3 位作者 潘军 蒋五玲 刘爱新 段明星 《Tsinghua Science and Technology》 SCIE EI CAS 1997年第1期33-35,共3页
Two brown spot disease resistant varieties of tobacco, named NC89 V1 and NC89 V2, were obtained by first inducing from disease sensitive NC89 with the two hypovirulent viruses ToMV N14 and CMV SV52, then tissue ... Two brown spot disease resistant varieties of tobacco, named NC89 V1 and NC89 V2, were obtained by first inducing from disease sensitive NC89 with the two hypovirulent viruses ToMV N14 and CMV SV52, then tissue culturing the plants and finally seed breeding. The disease resistance for both varieties was verified to be stable in three generations. The transcription activities of five plant defense response genes, pr 1a, chi, chs, pal, and lox, in NC89, NC89 V1, and NC89 V2 were studied through RNA blot hybridization. Genome DNA structural differences among the three tobacco lines were identified using randomly amplified polymorphic DNA(RAPD). 展开更多
关键词 induced disease resistance defense gene molecular basis
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Molecular basis of the high fidelity in protein synthesis
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作者 Jianping Ding Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue-Yang Road, Shanghai 200031, China 《生物物理学报》 CAS CSCD 北大核心 2009年第S1期81-81,共1页
Aminoacyl-tRNA synthetases (aaRSs) are a family of ancient enzymes that are responsible for catalysis of the attachment of amino acids to their cognate tRNAs in the first step
关键词 molecular basis of the high fidelity in protein synthesis HIGH
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Structural Analyses of Short-Chain Prenyltransfemses Identify an Evolutionarily Conserved GFPPS Clade in Brassicaceae Plants 被引量:21
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作者 ChengyuanWang Qingwen Chen +3 位作者 Dongjie Fan Jianxu Li Guodong Wang Peng Zhang 《Molecular Plant》 SCIE CAS CSCD 2016年第2期195-204,共10页
Terpenoids are the largest and most diverse class of plant-specialized metabolites, which function in diverse physiological processes during plant development. In the biosynthesis of plant terpenoids, short-chain pren... Terpenoids are the largest and most diverse class of plant-specialized metabolites, which function in diverse physiological processes during plant development. In the biosynthesis of plant terpenoids, short-chain prenyltransferases (SC-PTs), together with terpene synthases (TPSs), play critical roles in determining terpenoid diversity. SC-PTs biosynthesize prenyl pyrophosphates with different chain lengths, and these compounds are the direct precursors of terpenoids. Arabidopsis thaliana possesses a subgroup of SC-PTs whose functions are not clearly known. In this study, we focus on 10 geranylgeranyl pyro- phosphate synthase-like [GGPPSL] proteins, which are commonly thought to produce GGPP [C20]. We found that a subset of members of the Arabidopsis GGPPSL gene family have undergone neo- functionalization: GGPPSL6, 7, 9, and 10 mainly have geranylfarnesyl pyrophosphate synthase activity (C25; renamed AtGFPPS1, 2, 3, and 4), and GGPPSL8 produces even longer chain prenyl pyrophosphate (〉C30; renamed polyprenyl pyrophosphate synthase 2, AtPPPS2). By solving the crystal structures of AtGFPPS2, AtPPPS2, and AtGGPPS11, we reveal the product chain-length determination mechanism of SC-PTs and interpret it as a "three floors" model. Using this model, we identified a novel GFPPS clade distributed in Brassicaceae plants and found that the GFPPS gene typically occurs in tandem with a gene encoding a TPS, forming a GFPPS-TPS gene cluster. 展开更多
关键词 TERPENOID PRENYLTRANSFERASE molecular basis product length determination geranylfarnesyl diphos-phate synthase crystal structure
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Crystal clear: visualizing the intervention mechanism of the PD-1/PD-L1 interaction by two cancer therapeutic monoclonal antibodies 被引量:8
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作者 ShuguangTan Danqing Chen +9 位作者 Kefang Liu Mengnan He Hao Song Yi Shi Jun Liu Catherine W.-H. Zhang Jianxun Qi Jinghua Yan Shan Gao George F. Gao 《Protein & Cell》 SCIE CAS CSCD 2016年第12期866-877,共12页
Antibody-based PD-IIPD-L1 blockade therapies have taken center stage in immunotherapies for cancer, with multiple clinical successes. PD-1 signaling plays pivotal roles in tumor-driven T-cell dysfunction. In contrast ... Antibody-based PD-IIPD-L1 blockade therapies have taken center stage in immunotherapies for cancer, with multiple clinical successes. PD-1 signaling plays pivotal roles in tumor-driven T-cell dysfunction. In contrast to prior approaches to generate or boost tumor-specific T-cell responses, antibody-based PD-1/PD-L1 blockade targets tumor-induced T-cell defects and restores pre- existing T-cell function to modulate antitumor immunity. in this review, the fundamental knowledge on the expression regulations and inhibitory functions of PD-1 and the present understanding of antibody-based PD-1/ PD-L1 blockade therapies are briefly summarized. We then focus on the recent breakthrough work concerning the structural basis of the PD-IIPD-Ls interaction and how therapeutic antibodies, pembrolizumab targeting PD-1 and avelumab targeting PD-L1, compete with the binding of PD-1/PD-L1 to interrupt the PD-1/PD-L1 interaction. We believe that this structural informationwill benefit the design and improvement of therapeutic antibodies targeting PD-1 signaling. 展开更多
关键词 PD-1/PD-L1 interaction checkpointblockade molecular basis therapeutic antibody
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