Quality control in the endoplasmic reticulum
暂无分享,去创建一个
[1] I. Wada,et al. A novel ER α‐mannosidase‐like protein accelerates ER‐associated degradation , 2001 .
[2] A. J. Parodi,et al. Protein glucosylation and its role in protein folding. , 2000, Annual review of biochemistry.
[3] J. Rothman,et al. Biosynthetic protein transport and sorting by the endoplasmic reticulum and Golgi. , 1987, Annual review of biochemistry.
[4] F. Vogel,et al. ER-golgi traffic is a prerequisite for efficient ER degradation. , 2002, Molecular biology of the cell.
[5] Tommy Nilsson,et al. Short cytoplasmic sequences serve as retention signals for transmembrane proteins in the endoplasmic reticulum , 1989, Cell.
[6] S. Emr,et al. Ligand recognition and domain structure of Vps10p, a vacuolar protein sorting receptor in Saccharomyces cerevisiae. , 1999, European journal of biochemistry.
[7] D. Söll,et al. Quality control mechanisms during translation. , 1999, Science.
[8] T. Lindahl,et al. Quality control by DNA repair. , 1999, Science.
[9] J. Mackenzie,et al. Assembly and Maturation of the Flavivirus Kunjin Virus Appear To Occur in the Rough Endoplasmic Reticulum and along the Secretory Pathway, Respectively , 2001, Journal of Virology.
[10] R. Riek,et al. NMR structure of the calreticulin P-domain , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[11] E. Trombetta,et al. Calnexin, calreticulin and the folding of glycoproteins. , 1997, Trends in cell biology.
[12] K. Mori. Tripartite Management of Unfolded Proteins in the Endoplasmic Reticulum , 2000, Cell.
[13] H. Andersson,et al. The lectin ERGIC-53 is a cargo transport receptor for glycoproteins , 1999, Nature Cell Biology.
[14] W. Greene,et al. Cotranslational Biogenesis of NF-κB p50 by the 26S Proteasome , 1998, Cell.
[15] R. Schekman,et al. COPII and secretory cargo capture into transport vesicles. , 1997, Current opinion in cell biology.
[16] S. High,et al. Interaction of the Thiol-Dependent Reductase ERp57 with Nascent Glycoproteins , 1997, Science.
[17] J. Neefjes,et al. The major substrates for TAP in vivo are derived from newly synthesized proteins , 2000, Nature.
[18] A Helenius,et al. Setting the standards: quality control in the secretory pathway. , 1999, Science.
[19] M. Spiess,et al. Endoplasmic reticulum storage diseases. , 2002, Swiss medical weekly.
[20] S. High,et al. ERp57 functions as a subunit of specific complexes formed with the ER lectins calreticulin and calnexin. , 1999, Molecular biology of the cell.
[21] R. Schekman,et al. Out of the ER--outfitters, escorts and guides. , 1999, Trends in cell biology.
[22] J. Buchner,et al. Interaction of the chaperone BiP with an antibody domain: implications for the chaperone cycle. , 2002, Journal of Molecular Biology.
[23] Xi Chen,et al. ER stress regulation of ATF6 localization by dissociation of BiP/GRP78 binding and unmasking of Golgi localization signals. , 2002, Developmental cell.
[24] J. Goldstein,et al. Cholesterol addition to ER membranes alters conformation of SCAP, the SREBP escort protein that regulates cholesterol metabolism. , 2002, Molecular cell.
[25] L Orci,et al. Regulation of protein secretion through controlled aggregation in the endoplasmic reticulum. , 2000, Science.
[26] Yan Liu,et al. Oligosaccharide Modification in the Early Secretory Pathway Directs the Selection of a Misfolded Glycoprotein for Degradation by the Proteasome* , 1999, The Journal of Biological Chemistry.
[27] H. Kawasaki,et al. E3 ubiquitin ligase that recognizes sugar chains , 2002, Nature.
[28] S. Kornfeld,et al. The nonglycosylated glycoprotein of vesicular stomatitis virus is temperature-sensitive and undergoes intracellular aggregation at elevated temperatures. , 1979, The Journal of biological chemistry.
[29] J. Brodsky,et al. Assembly of ER-associated protein degradation in vitro: dependence on cytosol, calnexin, and ATP , 1996, The Journal of cell biology.
[30] G. Bu,et al. The roles of receptor-associated protein (RAP) as a molecular chaperone for members of the LDL receptor family. , 2001, International review of cytology.
[31] A. Helenius,et al. Glycoproteins form mixed disulphides with oxidoreductases during folding in living cells , 1999, Nature.
[32] J. Sambrook. The involvement of calcium in transport of secretory proteins from the endoplasmic reticulum , 1990, Cell.
[33] G. Wiens,et al. Recovering Antibody Secretion Using a Hapten Ligand as a Chemical Chaperone* , 2001, The Journal of Biological Chemistry.
[34] R. Riek,et al. TROSY-NMR reveals interaction between ERp57 and the tip of the calreticulin P-domain , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[35] Yoshihisa Hagihara,et al. Toward development of a screen to identify randomly encoded, foldable sequences , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[36] A. Ciechanover,et al. The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction. , 2002, Physiological reviews.
[37] Eric D. Spear,et al. Distinct retrieval and retention mechanisms are required for the quality control of endoplasmic reticulum protein folding , 2001, The Journal of cell biology.
[38] M R Jackson,et al. The Molecular Chaperone Calnexin Binds Glc1Man9GlcNAc2 Oligosaccharide as an Initial Step in Recognizing Unfolded Glycoproteins (*) , 1995, The Journal of Biological Chemistry.
[39] H. Hauri,et al. Mutations in the ER–Golgi Intermediate Compartment Protein ERGIC-53 Cause Combined Deficiency of Coagulation Factors V and VIII , 1998, Cell.
[40] M. R. Leach,et al. Calreticulin functions in vitro as a molecular chaperone for both glycosylated and non‐glycosylated proteins , 1999, The EMBO journal.
[41] William E. Balch,et al. Integration of endoplasmic reticulum signaling in health and disease , 1999, Nature Medicine.
[42] J. Yewdell,et al. At the crossroads of cell biology and immunology: DRiPs and other sources of peptide ligands for MHC class I molecules. , 2001, Journal of cell science.
[43] C. Kaiser,et al. A pathway for targeting soluble misfolded proteins to the yeast vacuole , 1996, The Journal of cell biology.
[44] J. Goldstein,et al. Insig-2, a second endoplasmic reticulum protein that binds SCAP and blocks export of sterol regulatory element-binding proteins , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[45] P. H. Cameron,et al. Association of folding intermediates of glycoproteins with calnexin during protein maturation , 1993, Nature.
[46] Jan C. Semenza,et al. ERD2, a yeast gene required for the receptor-mediated retrieval of luminal ER proteins from the secretory pathway , 1990, Cell.
[47] D. Clarke,et al. Correction of Defective Protein Kinesis of Human P-glycoprotein Mutants by Substrates and Modulators* , 1997, The Journal of Biological Chemistry.
[48] A. Verkman,et al. Diffusion in the Endoplasmic Reticulum of an Aquaporin-2 Mutant Causing Human Nephrogenic Diabetes Insipidus* , 2001, The Journal of Biological Chemistry.
[49] L. Hendershot,et al. A subset of chaperones and folding enzymes form multiprotein complexes in endoplasmic reticulum to bind nascent proteins. , 2002, Molecular biology of the cell.
[50] A. Helenius,et al. Quality control in the secretory pathway: retention of a misfolded viral membrane glycoprotein involves cycling between the ER, intermediate compartment, and Golgi apparatus , 1994, The Journal of cell biology.
[51] M. Bouvier,et al. Ligands act as pharmacological chaperones and increase the efficiency of δ opioid receptor maturation , 2002, The EMBO journal.
[52] A. Helenius,et al. Protein oligomerization in the endoplasmic reticulum. , 1989, Annual review of cell biology.
[53] D. Y. Thomas,et al. The Structure of calnexin, an ER chaperone involved in quality control of protein folding. , 2001, Molecular cell.
[54] A. Helenius,et al. Intracellular Assembly and Secretion of Recombinant Subviral Particles from Tick-Borne Encephalitis Virus , 2003, Journal of Virology.
[55] J. Brodsky,et al. ER protein quality control and proteasome-mediated protein degradation. , 1999, Seminars in cell & developmental biology.
[56] A. Varshavsky,et al. Detecting and measuring cotranslational protein degradation in vivo. , 2000, Science.
[57] G. de Prat-Gay,et al. UDP-Glc:glycoprotein glucosyltransferase recognizes structured and solvent accessible hydrophobic patches in molten globule-like folding intermediates , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[58] R. Halaban,et al. Proper Folding and Endoplasmic Reticulum to Golgi Transport of Tyrosinase Are Induced by Its Substrates, DOPA and Tyrosine* , 2001, The Journal of Biological Chemistry.
[59] S. Munro,et al. A C-terminal signal prevents secretion of luminal ER proteins , 1987, Cell.
[60] H. Pelham,et al. A transmembrane ubiquitin ligase required to sort membrane proteins into multivesicular bodies , 2002, Nature Cell Biology.
[61] H. Monaco,et al. Crystal structure of liganded and unliganded forms of bovine plasma retinol-binding protein. , 1994, The Journal of biological chemistry.
[62] Fred J. Stevens,et al. The In Vivo Association of BiP with Newly Synthesized Proteins Is Dependent on the Rate and Stability of Folding and Not Simply on the Presence of Sequences That Can Bind to BiP , 1999, The Journal of cell biology.
[63] A. Helenius,et al. Quality control in the endoplasmic reticulum: folding and misfolding of vesicular stomatitis virus G protein in cells and in vitro , 1990, The Journal of cell biology.
[64] S. Angers,et al. Pharmacological chaperones rescue cell-surface expression and function of misfolded V2 vasopressin receptor mutants. , 2000, The Journal of clinical investigation.
[65] W. Welch,et al. Correcting temperature-sensitive protein folding defects. , 1997, The Journal of clinical investigation.
[66] A. Helenius,et al. The Transitional ER Defines a Boundary for Quality Control in the Secretion of tsO45 VSV Glycoprotein , 2002, Traffic.
[67] H. Pelham. Using sorting signals to retain proteins in endoplasmic reticulum. , 2000, Methods in enzymology.
[68] S. Emr,et al. Coatomer is essential for retrieval of dilysine-tagged proteins to the endoplasmic reticulum , 1994, Cell.
[69] R D Klausner,et al. Building a multichain receptor: synthesis, degradation, and assembly of the T-cell antigen receptor. , 1987, Proceedings of the National Academy of Sciences of the United States of America.
[70] K D Wittrup,et al. Protein Folding Stability Can Determine the Efficiency of Escape from Endoplasmic Reticulum Quality Control* , 1998, The Journal of Biological Chemistry.
[71] L. Jan,et al. ER transport signals and trafficking of potassium channels and receptors , 2002, Current Opinion in Neurobiology.
[72] F. Wieland,et al. The secretory pathway: mechanisms of protein sorting and transport. , 1996, Biochimica et biophysica acta.
[73] M. Jackson,et al. Signal-mediated sorting of membrane proteins between the endoplasmic reticulum and the golgi apparatus. , 1996, Annual review of cell and developmental biology.
[74] S. Hubbard,et al. The structural aspects of limited proteolysis of native proteins. , 1998, Biochimica et biophysica acta.
[75] T. Rapoport,et al. Retro-translocation of proteins from the endoplasmic reticulum into the cytosol , 2002, Nature Reviews Molecular Cell Biology.
[76] D. Bichet,et al. Pharmacological chaperones: a new twist on receptor folding. , 2000, Trends in pharmacological sciences.
[77] S. Deschênes,et al. Intracellular transport, assembly, and degradation of wild-type and disease-linked mutant gap junction proteins. , 2000, Molecular biology of the cell.
[78] A. Helenius,et al. Conformational Requirements for Glycoprotein Reglucosylation in the Endoplasmic Reticulum , 2000, The Journal of cell biology.
[79] K D Wittrup,et al. Secretion efficiency in Saccharomyces cerevisiae of bovine pancreatic trypsin inhibitor mutants lacking disulfide bonds is correlated with thermodynamic stability. , 1998, Biochemistry.
[80] S. Gottesman,et al. Posttranslational quality control: folding, refolding, and degrading proteins. , 1999, Science.
[81] A. Helenius,et al. Role of N-linked oligosaccharide recognition, glucose trimming, and calnexin in glycoprotein folding and quality control. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[82] Y. Ihara,et al. Calnexin discriminates between protein conformational states and functions as a molecular chaperone in vitro. , 1999, Molecular cell.
[83] David Y. Thomas,et al. Htm1p, a mannosidase‐like protein, is involved in glycoprotein degradation in yeast , 2001, EMBO reports.
[84] A. Helenius,et al. Interaction of Newly Synthesized Apolipoprotein B with Calnexin and Calreticulin Requires Glucose Trimming in the Endoplasmic Reticulum , 1999, Bioscience reports.
[85] S. Sprang,et al. Affinity panning of a library of peptides displayed on bacteriophages reveals the binding specificity of BiP , 1993, Cell.
[86] P. Cresswell. Intracellular Surveillance: Controlling the Assembly of MHC Class I‐Peptide Complexes , 2000, Traffic.
[87] Christopher M Dobson,et al. Getting out of shape. , 2002, Nature.
[88] H. Söling,et al. Definition of the Lectin-like Properties of the Molecular Chaperone, Calreticulin, and Demonstration of Its Copurification with Endomannosidase from Rat Liver Golgi (*) , 1996, The Journal of Biological Chemistry.
[89] A. Parodi,et al. Immunolocalization of UDP-glucose:glycoprotein glucosyltransferase indicates involvement of pre-Golgi intermediates in protein quality control , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[90] K D Wittrup,et al. Yeast polypeptide fusion surface display levels predict thermal stability and soluble secretion efficiency. , 1999, Journal of molecular biology.
[91] C. Zuker,et al. The cyclophilin homolog ninaA is a tissue-specific integral membrane protein required for the proper synthesis of a subset of Drosophila rhodopsins , 1991, Cell.
[92] M. Bouvier,et al. Export from the Endoplasmic Reticulum Represents the Limiting Step in the Maturation and Cell Surface Expression of the Human δ Opioid Receptor* , 2000, The Journal of Biological Chemistry.
[93] H. Pelham. About turn for the COPs? , 1994, Cell.
[94] Takashi Saito,et al. The KDEL receptor mediates a retrieval mechanism that contributes to quality control at the endoplasmic reticulum , 2001, The EMBO journal.
[95] M. Torrisi,et al. Morphological analysis of the transfer of VSV ts-045 G glycoprotein from the endoplasmic reticulum to the intermediate compartment in vero cells. , 1996, Experimental cell research.
[96] T. Rapoport,et al. Unfolded cholera toxin is transferred to the ER membrane and released from protein disulfide isomerase upon oxidation by Ero1 , 2002, The Journal of cell biology.
[97] Jonathan W. Yewdell,et al. Rapid degradation of a large fraction of newly synthesized proteins by proteasomes , 2000, Nature.
[98] J. Rothman,et al. Peptide-binding specificity of the molecular chaperone BiP , 1991, Nature.
[99] R. Kopito,et al. Biosynthesis and degradation of CFTR. , 1999, Physiological reviews.
[100] Per Balschmidt,et al. Engineering-enhanced Protein Secretory Expression in Yeast with Application to Insulin* 210 , 2002, The Journal of Biological Chemistry.
[101] J. Rothman,et al. The capacity to retrieve escaped ER proteins extends to the trans-most cisterna of the Golgi stack , 1995, The Journal of cell biology.
[102] J. Merlie,et al. Assembly in vivo of mouse muscle acetylcholine receptor: Identification of an α subunit species that may be an assembly intermediate , 1983, Cell.
[103] R. Sitia,et al. Quality control of ER synthesized proteins: an exposed thiol group as a three‐way switch mediating assembly, retention and degradation. , 1993, The EMBO journal.
[104] P. A. Peterson,et al. Ligand-dependent secretion of rat retinol-binding protein expressed in HeLa cells. , 1992, The Journal of biological chemistry.
[105] Seng H. Cheng,et al. Intracellular protein trafficking defects in human disease. , 1992, Trends in cell biology.
[106] M. Molinari,et al. Sequential assistance of molecular chaperones and transient formation of covalent complexes during protein degradation from the ER , 2002, The Journal of cell biology.
[107] R. Spiro,et al. Golgi apparatus immunolocalization of endomannosidase suggests post-endoplasmic reticulum glucose trimming: implications for quality control. , 2000, Molecular biology of the cell.
[108] W. Balch,et al. Cargo Selection by the COPII Budding Machinery during Export from the ER , 1998, The Journal of cell biology.
[109] Christopher M. Dobson,et al. Protein-misfolding diseases: Getting out of shape , 2002, Nature.
[110] I. O'kelly,et al. Forward Transport 14-3-3 Binding Overcomes Retention in Endoplasmic Reticulum by Dibasic Signals , 2002, Cell.
[111] M. Jackson,et al. Identification of a consensus motif for retention of transmembrane proteins in the endoplasmic reticulum. , 1990, The EMBO journal.
[112] Ruth Geiss-Friedlander,et al. Protein Dislocation from the Endoplasmic Reticulum – Pulling Out the Suspect , 2002, Traffic.
[113] A. Luini,et al. Small cargo proteins and large aggregates can traverse the Golgi by a common mechanism without leaving the lumen of cisternae , 2001, The Journal of cell biology.
[114] Randy Schekman,et al. COPII–cargo interactions direct protein sorting into ER-derived transport vesicles , 1998, Nature.
[115] T. Steck,et al. SCAP, an ER sensor that regulates cell cholesterol. , 2002, Developmental cell.
[116] M. R. Leach,et al. Localization of the Lectin, ERp57 Binding, and Polypeptide Binding Sites of Calnexin and Calreticulin* , 2002, The Journal of Biological Chemistry.
[117] George Palade,et al. Intracellular Aspects of the Process of Protein Synthesis , 1975, Science.
[118] M. Edidin,et al. Probing for membrane domains in the endoplasmic reticulum: retention and degradation of unassembled MHC class I molecules. , 2002, Molecular biology of the cell.
[119] C. Rodighiero,et al. Protein Disulfide Isomerase Acts as a Redox-Dependent Chaperone to Unfold Cholera Toxin , 2001, Cell.
[120] C. Kurland,et al. Translational accuracy and the fitness of bacteria. , 1992, Annual review of genetics.
[121] A. Helenius,et al. Recognition of local glycoprotein misfolding by the ER folding sensor UDP-glucose:glycoprotein glucosyltransferase , 2000, Nature Structural Biology.
[122] A. Cooper,et al. Degradation of Endoplasmic Reticulum (ER) Quality Control Substrates Requires Transport between the ER and Golgi* , 2001, The Journal of Biological Chemistry.
[123] G. Koch,et al. Perturbation of cellular calcium induces secretion of luminal ER proteins , 1989, Cell.
[124] E. Carlier,et al. The I-II Loop of the Ca2+ Channel α1 Subunit Contains an Endoplasmic Reticulum Retention Signal Antagonized by the β Subunit , 2000, Neuron.
[125] R. Aebersold,et al. Crucial Step in Cholesterol Homeostasis Sterols Promote Binding of SCAP to INSIG-1, a Membrane Protein that Facilitates Retention of SREBPs in ER , 2002, Cell.
[126] Ari Helenius,et al. Glucose trimming and reglucosylation determine glycoprotein association with calnexin in the endoplasmic reticulum , 1995, Cell.
[127] Michele C. Kieke,et al. Directed evolution of a stable scaffold for T-cell receptor engineering , 2000, Nature Biotechnology.
[128] Jan Ellenberg,et al. Dynamics and retention of misfolded proteins in native ER membranes , 2000, Nature Cell Biology.
[129] Y. Jan,et al. A New ER Trafficking Signal Regulates the Subunit Stoichiometry of Plasma Membrane KATP Channels , 1999, Neuron.
[130] R. Klausner,et al. Protein degradation in the endoplasmic reticulum , 1990, Cell.
[131] C. Barlowe. COPII-dependent transport from the endoplasmic reticulum. , 2002, Current opinion in cell biology.
[132] U. Danilczyk,et al. The Lectin Chaperone Calnexin Utilizes Polypeptide-based Interactions to Associate with Many of Its Substrates in Vivo * , 2001, The Journal of Biological Chemistry.