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The endoplasmic reticulum or ER makes up for more than half of the membranes in a cell and accounts for 10% of total cell volume. It is also the primary protein and lipid synthesis factory for most cell organelles, such as the Golgi apparatus, lysosomes, secretory vesicles, and the plasma membrane. Despite being the most extensive and functionally complex subcellular organelle, ER was the last to be discovered. After years of deliberation, Keith Porter and George Palade in the year 1954, produced the first high-resolution electron microscope images to affirm the presence of ER in the eukaryotic cell.

The ER membranes were identified as sites for protein synthesis and crucial for intracellular transport using radio-labeled and fluorescent-labeled amino acids. The isolation of ER is a tricky task as it forms an intricate mesh with other subcellular organelles. However, on cell homogenization, the disrupted ER membranes reseal into small closed vesicles called microsomes. These vesicles form a microsystem capable of sustaining all ER-related functions like protein and lipid synthesis, calcium signaling, and glycosylation. Subcellular fractionation is the best and often-used technique for the purification of these membranes. When separating using a sucrose gradient, the rough ER microsomes sediments at a higher density than smooth ER microsomes.

The ER network in a cell is dynamic. It is constantly shape-shifting along with the cytoskeleton to bolster mechanical support for the cell structure. Despite the distinct cisternae and tubule morphologies of the ER membrane, interconversion between the two is possible and is governed by the expression of membrane proteins. The ER network rearranges by tubule growth, retraction, and fusion of adjacent ER-ER membranes.

As mentioned above, the ER network is required for optimal overall cellular health. Disruption of ER morphology is linked to pathological conditions, including neurological disorders like Alzheimer's disease, hereditary spastic paraplegia, and viral infections like hepatitis C virus, and dengue virus.

Tags
Endoplasmic ReticulumERProtein SynthesisLipid SynthesisIntracellular TransportMicrosomesSubcellular FractionationRough ERSmooth ERER NetworkER MorphologyCellular HealthNeurological DisordersViral Infections

Aus Kapitel 15:

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15.1 : Das endoplasmatische Retikulum

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15.2 : Glattes endoplasmatisches Retikulum

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15.3 : Die Rolle des ER im sekretorischen Weg

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15.4 : Die Lenkung von Proteinen zum rauen endoplasmatischen Retikulum

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15.5 : Mechanismen der Proteintranslokation an der ER-Membran

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15.6 : Cotranslationale Translokation von Proteinen

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15.7 : Posttranslationale Translokation von Proteinen in das RER

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15.8 : Einbringung von Single-Pass-Transmembranproteinen in das RER

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15.9 : Einbringung von Multi-Pass-Transmembranproteinen in das RER

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15.10 : Endverankerung von Proteinen in der ER-Membran

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15.11 : GPI-Verankerung von Proteinen in der ER-Membran

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15.12 : Proteinmodifikationen im RER

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15.13 : Qualitätskontrolle der Proteinfaltung im RER

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15.14 : Export von fehlgefalteten Proteinen aus dem ER

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15.15 : Die ungefaltete Proteinantwort

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