Protein Tyrosine Phosphatase Control of Metabolism

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Publisher : Springer Science & Business Media
ISBN 13 : 1461478553
Total Pages : 279 pages
Book Rating : 4.4/5 (614 download)

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Book Synopsis Protein Tyrosine Phosphatase Control of Metabolism by : Kendra K. Bence

Download or read book Protein Tyrosine Phosphatase Control of Metabolism written by Kendra K. Bence and published by Springer Science & Business Media. This book was released on 2013-08-30 with total page 279 pages. Available in PDF, EPUB and Kindle. Book excerpt: Although phosphorylation of proteins on tyrosine is relatively rare compared to phosphorylation on serine or threonine residues, the past two decades of research into PTP function have led to a great appreciation of the critical role PTPs have in regulating basic cellular processes. Among these important roles is the regulation of cellular signaling pathways related to metabolism. This volume contains chapters which highlight many aspects of PTP function in the context of metabolism. Given the growing obesity and diabetes epidemics in the United States and throughout the world, the desire to identify possible therapeutic targets for treatment of these diseases is a high priority. In many ways, PTPs may be attractive drug targets since they are amenable to targeting with small molecules; however many challenges abound in making PTP inhibitors.

Diabetes Mellitus

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Publisher : Lippincott Williams & Wilkins
ISBN 13 : 9780781740975
Total Pages : 1606 pages
Book Rating : 4.7/5 (49 download)

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Book Synopsis Diabetes Mellitus by : Derek LeRoith

Download or read book Diabetes Mellitus written by Derek LeRoith and published by Lippincott Williams & Wilkins. This book was released on 2004 with total page 1606 pages. Available in PDF, EPUB and Kindle. Book excerpt: Thoroughly revised and updated, this Third Edition encompasses the most recent advances in molecular and cellular research and describes the newest therapeutic modalities for type 1 and type 2 diabetes mellitus. Chapters by leading experts integrate the latest basic science and clinical research on diabetes mellitus and its complications. The text is divided into ten major sections, including extensive sections on therapeutics, diabetes during pregnancy, and complications. New chapters cover stem cell therapy for type 1 diabetes; genetics and treatment of obesity; new therapies to promote insulin action; vasculopathy; islet cell protocols; triglycerides in muscle; hypoglycemia in the adult; and the Diabetes Prevention Program.

Protein Tyrosine Phosphatases

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Publisher : Walter de Gruyter GmbH & Co KG
ISBN 13 : 3110421771
Total Pages : 296 pages
Book Rating : 4.1/5 (14 download)

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Book Synopsis Protein Tyrosine Phosphatases by : Lalima G. Ahuja

Download or read book Protein Tyrosine Phosphatases written by Lalima G. Ahuja and published by Walter de Gruyter GmbH & Co KG. This book was released on 2018-10-08 with total page 296 pages. Available in PDF, EPUB and Kindle. Book excerpt: Protein tyrosine phosphatases remove phosphates from the phosphotyrosine residues of target proteins and reverse the action of various protein tyrosine kinases. This essential interplay between the opposing actions of protein tyrosine phosphatases and protein tyrosine kinases forms the basis of signaling networks that underlie the cellular workings of human physiology. Initially passed-off as housekeeping genes; these proteins were only acknowledged to maintain a steady background of phosphotyrosine levels in the cell. However, recent progress in studying their role in embryonic development and human disease has established their importance as regulators of signal regulation. Convincing evidence shows the role of mutations in these proteins to cause and/or intensify the severity of various diseases including metabolic and neurological disorders and also cancer. Protein tyrosine phosphatases have slowly, yet convincingly become crucial targets for therapeutic intervention of various human pathophysiologies. This book describes these signaling enzymes using the molecular details of their structure and mechanistic function. Various subtypes of cysteine-based Class I, II, III and the Haloacid dehalogenase related Class IV protein tyrosine phosphatases have been illustrated and explained. The superfamily of proteins is also described vis-a-vis its complimentary protein phosphoserine/phosphoserine phosphatases. Membrane bound receptor forms and the cytosolic non-receptor protein tyrosine phosphatases have been described for their biological function. This book serves as a reference for any reader looking to understand the sequence features, structural elements, molecular mechanism and cellular function of this superfamily of signaling enzymes.

Bridging the Gap Between Protein-tyrosine Phosphorylation Networks, Metabolism and Physiology in Liver-specific PTP1b Deletion Mice

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Publisher :
ISBN 13 :
Total Pages : 182 pages
Book Rating : 4.:/5 (86 download)

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Book Synopsis Bridging the Gap Between Protein-tyrosine Phosphorylation Networks, Metabolism and Physiology in Liver-specific PTP1b Deletion Mice by : Emily Rae Miraldi

Download or read book Bridging the Gap Between Protein-tyrosine Phosphorylation Networks, Metabolism and Physiology in Liver-specific PTP1b Deletion Mice written by Emily Rae Miraldi and published by . This book was released on 2012 with total page 182 pages. Available in PDF, EPUB and Kindle. Book excerpt: Metabolic syndrome describes a complex set of obesity-related disorders that enhance diabetes, cardiovascular, and mortality risk. Studies of liver-specific protein-tyrosine phosphatase lb (PTPlb) deletion mice (L-PTPlb-/-) suggests that hepatic PTPlb inhibition would mitigate metabolic syndrome progression through amelioration of hepatic insulin resistance, endoplasmic reticulum stress, and whole-body lipid metabolism. However, the network alterations underlying these phenotypes are poorly understood. Mass spectrometry was used to quantitatively discover protein phosphotyrosine network changes in L-PTP lb-/- mice relative to control mice under both normal and high-fat diet conditions. A phosphosite set enrichment analysis was developed to identify numerous pathways exhibiting PTPlb- and diet-dependent phosphotyrosine regulation. Detection of PTP lb-dependent phosphotyrosine sites on lipid metabolic proteins initiated global lipidomics characterization of corresponding liver samples and revealed altered fatty acid and triglyceride metabolism in L-PTPlb-/- mice. Multivariate modeling techniques were developed to infer molecular dependencies between phosphosites and lipid metabolic changes, resulting in quantitatively predictive phenotypic models.

Investigations Into the Chemistry of Protein Tyrosine Phosphatase Redox Regulation

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Publisher :
ISBN 13 :
Total Pages : 148 pages
Book Rating : 4.:/5 (518 download)

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Book Synopsis Investigations Into the Chemistry of Protein Tyrosine Phosphatase Redox Regulation by : Jason N. LaButti

Download or read book Investigations Into the Chemistry of Protein Tyrosine Phosphatase Redox Regulation written by Jason N. LaButti and published by . This book was released on 2009 with total page 148 pages. Available in PDF, EPUB and Kindle. Book excerpt: Transmission of complex intracellular signals, such as those for glucose uptake or proliferation, is often accomplished through the reversible phosphorylation of specific protein tyrosine residues. This reversible phosphorylation serves as a biochemical "rheostat" that alters a protein's functional properties and leads to propagation of the signal. The phosphorylation status of these tyrosine residues, thus transmission of the cellular signal itself, is tightly controlled by the opposing actions of protein tyrosine kinases that catalyze the addition of phosphoryl groups and protein tyrosine phosphatases (PTPs) are cysteine based enzymes that catalyze their removal. Abstraction of these phosphoryl groups, in many cases, serves as an "off switch" to terminate the cellular responses to the extracellular stimulus. PTPs, therefore, play a central role in the regulation of diverse cellular processes including glucose metabolism, cell cycle control and immune responses. Accordingly, small molecules capable of inactivating PTPs through reversible oxidation of their active site cysteine thiolate may find use as therapeutic agents and/or tools for the study of diverse signal transduction pathways. In the body of work presented here we report the chemical properties of a novel PTP redox regulator and develop new methodologies for studying PTP redox regulation.

Protein Tyrosine Phosphatases

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Publisher : Springer Nature
ISBN 13 : 1071635697
Total Pages : 321 pages
Book Rating : 4.0/5 (716 download)

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Book Synopsis Protein Tyrosine Phosphatases by : Damien Thévenin

Download or read book Protein Tyrosine Phosphatases written by Damien Thévenin and published by Springer Nature. This book was released on 2024-01-27 with total page 321 pages. Available in PDF, EPUB and Kindle. Book excerpt: This second edition volume expands on the previous edition with discussions on the latest advancements in protein tyrosine phosphatases (PTP) research used to investigate these essential enzymes and new inhibitors. The new techniques covered in the chapters of this book include studying enzymes in vitro, in cells, and in animal models through proteomics, genomics, and structural biology. Furthermore, new advances in pharmacology and drug design have contributed to the developing novel therapeutics that target PTPs. Written in the highly successful Methods in Molecular Biology series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. Cutting-edge and comprehensive, Protein Tyrosine Phosphatases: Methods and Protocols, Second Edition is a valuable resource for both experienced and novel researchers in this field, and will lead to discoveries and accelerated progress in the field of PTP, signal transduction, and drug development.

Molecular Biology of Prostate Cancer

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Publisher : Walter de Gruyter
ISBN 13 : 3110807270
Total Pages : 220 pages
Book Rating : 4.1/5 (18 download)

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Book Synopsis Molecular Biology of Prostate Cancer by : Manfred Wirth

Download or read book Molecular Biology of Prostate Cancer written by Manfred Wirth and published by Walter de Gruyter. This book was released on 2013-05-22 with total page 220 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Roles of Protein-tyrosine Phosphatases in the Endocrine Pancreas

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Publisher :
ISBN 13 : 9781303541223
Total Pages : pages
Book Rating : 4.5/5 (412 download)

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Book Synopsis Roles of Protein-tyrosine Phosphatases in the Endocrine Pancreas by : Yannan Xi

Download or read book Roles of Protein-tyrosine Phosphatases in the Endocrine Pancreas written by Yannan Xi and published by . This book was released on 2013 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Protein-tyrosine phosphatase 1B (PTP1B) and T cell protein-tyrosine phosphatase (TCPTP) are structurally similar cytosolic proteins that are implicated in the regulation of metabolism. PTP1B is an important physiological regulator of glucose homeostasis and energy balance and the role of PTP1B in liver, muscle, and brain has been established. TCPTP is implicated in cytokine-induced pancreatic beta-cell apoptosis and is a candidate gene in type 1 diabetes. However, the roles of PTP1B and TCPTP in pancreatic endocrine function and insulin secretion remain largely unknown. To explore the metabolic role of PTP1B in the pancreas, we generated mice with pancreas-specific PTP1B deletion (panc-PTP1B KO) and fed them chow or high fat diet (HFD) and evaluated their glucose tolerance and insulin secretion. Insulin secretion and biochemical studies were performed on isolated islets and MIN6 cells with knockdown (KD) and reconstituted PTP1B. On regular chow, aged panc-PTP1B KO mice exhibited glucose intolerance compared with controls. HFD led to earlier impairment of glucose tolerance and attenuated glucose-stimulated insulin secretion (GSIS) in panc-PTP1B KO mice. Ex vivo studies demonstrated attenuated GSIS in KO islets and in MIN6 cells with PTP1B knockdown indicating a cell autonomous defect. Mechanistically, basal and glucose-stimulated EphA5 tyrosyl phosphorylation was enhanced in PTP1B deficient islets and in MIN6 cells with PTP1B knockdown. PTP1B reconstitution in KD cells attenuated EphA5 phosphorylation indicating that it is regulated by PTP1B. Moreover, EphA5 mutagenesis revealed that various tyrosine residues differentially modulate insulin secretion, and demonstrated that PTP1B directly regulates insulin secretion, at least in part, via EphA5. Collectively, our studies identify a novel role for pancreatic PTP1B and uncover EphA5 as a physiologically-relevant target for PTP1B. To investigate the metabolic role of TCPTP in pancreatic endocrine function, we generated mice with TCPTP deletion (panc-TCPTP KO). Mice were fed regular chow and HFD and insulin secretion and glucose homeostasis were determined. When fed regular chow diet panc-TCPTP KO mice exhibited comparable glucose tolerance to controls. On the other hand, when challenged with prolonged HFD panc-TCPTP KO mice exhibited impaired glucose tolerance and attenuated glucose-stimulated insulin secretion (GSIS) compared with controls. Ex vivo studies using primary islets demonstrated attenuated GSIS in panc-TCPTP KO islets compared with controls indicating that the effects are cell autonomous. In addition, lentiviral-mediated knockdown of TCPTP in the glucose-responsive MIN6 beta-cells attenuated GSIS while reconstitution of TCPTP restored GSIS to levels compared with controls demonstrating that the effects are directly caused by TCPTP deficiency. Similarly, pharmacological inhibition of TCPTP in Min6 cells attenuated GSIS. At the molecular level we identified STAT 1/3 as direct TCPTP substrates and modulators of its functions in beta-cells. In summary, these studies identify a novel role for TCPTP in insulin secretion and uncover STAT3 as physiologically-relevant target for TCPTP in the pancreas.

Handbook of Cell Signaling

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Publisher : Academic Press
ISBN 13 : 0080920918
Total Pages : 3188 pages
Book Rating : 4.0/5 (89 download)

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Book Synopsis Handbook of Cell Signaling by : Ralph A. Bradshaw

Download or read book Handbook of Cell Signaling written by Ralph A. Bradshaw and published by Academic Press. This book was released on 2009-11-03 with total page 3188 pages. Available in PDF, EPUB and Kindle. Book excerpt: Handbook of Cell Signaling, Three-Volume Set, 2e, is a comprehensive work covering all aspects of intracellular signal processing, including extra/intracellular membrane receptors, signal transduction, gene expression/translation, and cellular/organotypic signal responses. The second edition is an up-to-date, expanded reference with each section edited by a recognized expert in the field. Tabular and well illustrated, the Handbook will serve as an in-depth reference for this complex and evolving field. Handbook of Cell Signaling, 2/e will appeal to a broad, cross-disciplinary audience interested in the structure, biochemistry, molecular biology and pathology of cellular effectors. Contains over 350 chapters of comprehensive coverage on cell signaling Includes discussion on topics from ligand/receptor interactions to organ/organism responses Provides user-friendly, well-illustrated, reputable content by experts in the field

Hydrogen Peroxide and Cell Signaling, Part B

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Publisher : Academic Press
ISBN 13 : 9780124058828
Total Pages : 0 pages
Book Rating : 4.0/5 (588 download)

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Book Synopsis Hydrogen Peroxide and Cell Signaling, Part B by :

Download or read book Hydrogen Peroxide and Cell Signaling, Part B written by and published by Academic Press. This book was released on 2013-07-15 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: This new volume of Methods in Enzymology continues the legacy of this premier serial with quality chapters authored by leaders in the field. This is the second of three volumes on hydrogen peroxide and cell signaling, and includes chapters on such topics as the cellular steady-state of H2O2, evaluating peroxiredoxin sensitivity towards inactivation by peroxide substrates, and peroxiredoxins as preferential targets in H2O2-induced signaling.

Protein Tyrosine Kinases

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Publisher : Springer Science & Business Media
ISBN 13 : 1592599621
Total Pages : 599 pages
Book Rating : 4.5/5 (925 download)

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Book Synopsis Protein Tyrosine Kinases by : Doriano Fabbro

Download or read book Protein Tyrosine Kinases written by Doriano Fabbro and published by Springer Science & Business Media. This book was released on 2007-11-13 with total page 599 pages. Available in PDF, EPUB and Kindle. Book excerpt: Leading researchers, from the Novartis group that pioneered Gleevec/GlivecTM and around the world, comprehensively survey the state of the art in the drug discovery processes (bio- and chemoinformatics, structural biology, profiling, generation of resistance, etc.) aimed at generating PTK inhibitors for the treatment of various diseases, including cancer. Highlights include a discussion of the rationale and the progress made towards generating "selective" low molecular-weight kinase inhibitors; an analysis of the normal function, role in disease, and application of platelet-derived growth factor antagonists; and a summary of the factors involved in successful structure-based drug design. Additional chapters address the advantages and disadvantages of in vivo preclinical models for testing protein kinase inhibitors with antitumor activity and the utility of different methods in the drug discovery and development process for determining "on-target" vs "off-target" effects of kinase inhibitors.

The Metabolic Effects of Novel Protein Tyrosine Phosphatase 1B (PTP1B) Substrates

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Publisher :
ISBN 13 : 9781321362060
Total Pages : pages
Book Rating : 4.3/5 (62 download)

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Book Synopsis The Metabolic Effects of Novel Protein Tyrosine Phosphatase 1B (PTP1B) Substrates by : Jesse Bakke

Download or read book The Metabolic Effects of Novel Protein Tyrosine Phosphatase 1B (PTP1B) Substrates written by Jesse Bakke and published by . This book was released on 2014 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Protein tyrosine phosphorylation is a covalent modification by protein tyrosine kinases and opposed by protein tyrosine phosphatases (PTPs). Protein phosphorylation is an important regulator of cell signaling pathways in all life forms and aberrant changes of phosphorylated proteins are often associated with diseases, such as cancer and metabolic diseases: obesity and type II diabetes. Importantly, there are over one hundred identified PTPs strictly defined with an active-site signature motif of HCX5R. Out of the one hundred total PTPs, thirty-seven are classical PTPs that are either transmembrane receptor-like PTPs or non-transmembrane PTPs. Protein tyrosine phosphatase 1B (PTP1B) is a non-transmembrane PTP, bound to the cytoplasmic face of endoplasmic reticulum with a C-terminal anchor. PTP1B has several well- known substrates, including the insulin receptor and insulin receptor substrate 1 (IRS1). PTP1B gained popularity as a therapeutic target due to the striking phenotype observed in mice following PTP1B gene deletion. The mice exhibited improved insulin sensitivity and decreased body weight upon high fat diet (HFD) feeding. Through tissue specific deletion, it was revealed that PTP1B has cell/tissue specific roles. Briefly, PTP1B deletion from muscle and liver results in improved insulin sensitivity and neuronal deletion of PTP1B results in resistance to HFD- induced obesity. Adipose specific deletion of PTP1B remains controversial with several contradictory reports; this argues for further work to be done to determine PTP1Bs role within adipose tissue. This dissertation uncovers novel PTP1B substrates in the adipose, syntaxin binding protein 3 (munc18c) and pyruvate kinase M2 (PKM2), and highlights the regulatory role of PTP1B in glucose transporter 4 (GLUT4) externalization as well as glycolytic flux. And surprisingly, PKM2 deficiency results in the emergence of a thermogenic program in white adipocytes.

Insulin Action

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Publisher : Springer Science & Business Media
ISBN 13 : 9780792381136
Total Pages : 206 pages
Book Rating : 4.3/5 (811 download)

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Book Synopsis Insulin Action by : Ashok K. Srivastava

Download or read book Insulin Action written by Ashok K. Srivastava and published by Springer Science & Business Media. This book was released on 1998-05-31 with total page 206 pages. Available in PDF, EPUB and Kindle. Book excerpt: In 1996 the 75th anniversary of the discovery of insulin was celebrated at the University of Toronto, the scene of that discovery in 1921. This volume was stimulated by the scientific program which was staged at that time and brought together much of the world's best talent to discuss and analyze the most recent developments in our understanding of pancreatic function, insulin secretion, the interaction of insulin with its target tissues, the mechanism of insulin action at the cellular level, and the defects which underlie both Type I (insulin-dependent diabetes mellitus, IDDM) and Type II (noninsulin-dependent diabetes mellitus, NIDDM) forms of the disease. We have chosen to focus the present volume on work related to insulin action.

Prokaryotic Metabolism and Physiology

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Publisher : Cambridge University Press
ISBN 13 : 1107171733
Total Pages : 509 pages
Book Rating : 4.1/5 (71 download)

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Book Synopsis Prokaryotic Metabolism and Physiology by : Byung Hong Kim

Download or read book Prokaryotic Metabolism and Physiology written by Byung Hong Kim and published by Cambridge University Press. This book was released on 2019-05-16 with total page 509 pages. Available in PDF, EPUB and Kindle. Book excerpt: Extensive and up-to-date review of key metabolic processes in bacteria and archaea and how metabolism is regulated under various conditions.

Protein Tyrosine Phosphatases in Cancer

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Publisher : Springer
ISBN 13 : 1493936492
Total Pages : 362 pages
Book Rating : 4.4/5 (939 download)

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Book Synopsis Protein Tyrosine Phosphatases in Cancer by : Benjamin G. Neel

Download or read book Protein Tyrosine Phosphatases in Cancer written by Benjamin G. Neel and published by Springer. This book was released on 2016-08-05 with total page 362 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book aims to bridge the gap in understanding how protein-tyrosine phosphatases (PTPs), which carry out the reverse reaction of tyrosine phosphorylation, feature in cancer cell biology. The expertly authored chapters will first review the general features of the PTP superfamily, including their overall structure and enzymological properties; use selected examples of individual PTP superfamily members, to illustrate emerging data on the role of PTPs in cancer; and will review the current status of PTP-based drug development efforts. Protein Tyrosine Phosphatases in Cancer,from renowned researchers Benjamin Neel and Nicholas Tonks, is invaluable reading for researchers in oncology, stem cell signaling,and biochemistry.

Inactivation of Protein Tyrosine Phosphatases by Endogenous and Dietary Agents

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Publisher :
ISBN 13 :
Total Pages : 133 pages
Book Rating : 4.:/5 (519 download)

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Book Synopsis Inactivation of Protein Tyrosine Phosphatases by Endogenous and Dietary Agents by : Derrick R. Seiner

Download or read book Inactivation of Protein Tyrosine Phosphatases by Endogenous and Dietary Agents written by Derrick R. Seiner and published by . This book was released on 2009 with total page 133 pages. Available in PDF, EPUB and Kindle. Book excerpt: Protein tyrosine phosphatases are a class of enzymes that control a number of critical signaling pathways inside cells. We have discovered a number of dietary and endogenous agents that are capable of modifying these enzymes, and therefore disrupting signaling pathways inside cells. It is possible that these small molecules are exerting their widely reported biological effect by the modification of protein tyrosine phosphatase activity. This information is critical to our understanding of dietary effect on diseases like diabetes and cancer. In addition to this work, we have explored the chemistry of the most common DNA lesion, the abasic site. We have found it is capable of producing an interstrand crosslink in duplex DNA, when placed in the right sequence context. This work significantly expands our understanding of the toxicity of abasic sites to cells. Furthermore, this work may result in developing novel treatment strategies for cancer.

Regulation of Protein Tyrosine Phosphatases by Glucose

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Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (133 download)

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Book Synopsis Regulation of Protein Tyrosine Phosphatases by Glucose by : Hoang Kim Le-Tien

Download or read book Regulation of Protein Tyrosine Phosphatases by Glucose written by Hoang Kim Le-Tien and published by . This book was released on 2000 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: Exposure of tissues to high glucose concentrations (HG) induces a number of alterations in cell signalling. The role in these effects of protein tyrosine phosphatases (PTPs), key enzymes regulating the extent and duration of tyrosine phosphorylation, has not been studied. 'Hypothesis'. HG will cause changes in PTP expression and activity which contribute to the effects of HG on signalling. 'Results'. Exposure of rat adipocytes to HG with insulin and cultured rat mesangial cells (MCs) to HG caused an increase in protein content of transmembrane PTPÃ, but no change in the intracellular SHP2 or PTP1B. Transmernbrane PTP LAR was detected only in adipocytes and was decreased. Specific activity of PTPÃ was not altered in adipocytes, but decreased in MCs. HG is thought to modulate its effects in MCs by PKC activation and PKC downregulation with phorbol myristate acetate blocked the increased in PTPÃ by HG. The cytosolic tyrosine kinase Src, a substrate of and activated by PTPÃ, was increased by HG in protein but specific activity was decreased by HQ consistent with decreased activity of PTPÃ. 'Conclusion'. HG causes changes in cellular PTPs which may contribute to the altered signalling observed.