In: Cells, 2020, vol. 9, no. 9, p. 11 p
The endoplasmic reticulum (ER) is site of synthesis and maturation of membrane and secretory proteins in eukaryotic cells. The ER contains more than 20 members of the Protein Disulfide Isomerase (PDI) family. These enzymes regulate formation, isomerization and disassembly of covalent bonds between cysteine residues. As such, PDIs ensure protein folding, which is required to attain functional...
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In: DNA and cell biology
Hunter’s syndrome (mucopolysaccharidosis type II) is a rare X-linked lysosomal storage disorder caused by mutations in the iduronate 2-sulfatase (IDS) gene. Motivated by the case of a child affected by this syndrome, we compared the intracellular fate of wild type IDS (IDSWT) and of four nonsense mutations of IDS (IDSL482X, IDSY452X, IDSR443X and IDSW337X) generating progressively shorter ...
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In: Nature communications, 2019, vol. 10, p. 5058
The endoplasmic reticulum (ER) produces about 40% of the nucleated cell’s proteome. ER size and content in molecular chaperones increase upon physiologic and pathologic stresses on activation of unfolded protein responses (UPR). On stress resolution, the mammalian ER is remodeled to pre-stress, physiologic size and function on activation of the LC3-binding activity of the translocon...
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In: Journal of rare diseases research & treatment, 2016, vol. 1, no. 1, p. 40-42
Human proteinopathies are diseases caused by the expression of defective gene products. In some cases, these diseases involve the degradation of mutant but otherwise functional proteins by the quality control system of the secretory pathway. Our recent study identified two proteins that play a role in post-endoplasmic reticulum (ER) quality control and are potential targets for therapeutic ...
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In: Histochemistry and Cell Biology, 2014, vol. 142, no. 2, p. 153-169
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In: Protoplasma, 1999, vol. 207, no. 3-4, p. 141-146
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In: Protoplasma, 2011, vol. 248, no. 1, p. 75-99
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In: Histochemistry and Cell Biology, 2007, vol. 128, no. 2, p. 161-173
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In: Cellular and Molecular Life Sciences, 2013, vol. 70, no. 11, p. 1985-2002
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In: Journal of Cell Science, 2011, vol. 124, p. 2424-2437
Cells store metabolic energy in the form of neutral lipids that are deposited within lipid droplets (LDs). In this study, we examine the biogenesis of LDs and the transport of integral membrane proteins from the endoplasmic reticulum (ER) to newly formed LDs. In cells that lack LDs, otherwise LD-localized membrane proteins are homogenously distributed in the ER membrane. Under these conditions,...
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