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#vesicles

2 public questions tagged with this topic.

Which face of the Golgi apparatus is responsible for receiving vesicles from the ER?

Golgi polarity defined by cis entry face adjacent to ER exit sites and trans exit face oriented toward plasma membrane. Newly synthesized cargo packaged into COPII coated vesicles decorated with Sec23/24 cargo selection and Sar1 GTPase buds from ER after BiP quality control, fuses via TRAPP tethering to ER-Golgi intermediate compartment then to cis Golgi network marked by Rab1 and cis golgin GM130 and GRASP65. Here resident enzymes mannosidase I and N-acetylglucosamine transferase I begin processing, and retrieval of ER proteins via KDEL receptor and COPI retrograde occurs. Medial cisternae continue glycosylation, trans cisternae add galactose sialic acid and sulfation. Finally trans Golgi network defined by clathrin adaptors AP1, GGA sorts cargo to lysosomes or constitutive secretion. Time-lapse tracking of temperature-sensitive VSV-G shows arrival at cis within five minutes from ER release, traversing stacks in about twenty minutes, confirming cis as receiving face. Maturation face term describes cisternal progression model, but receiving function clearly cis, opposite orientation would reverse secretory direction.

Ref: Lippincott-S Cell Bio; COPII ER exit to cis Golgi CGN receives cargo, Rab1, VSV-G trafficking.

Microsomes are artificially formed vesicles derived from:

Cell fractionation pioneered by Claude and Palade showed that mechanical homogenization shears endoplasmic reticulum tubular network into small vesicles that reseal spontaneously due to energetically unfavorable exposed hydrophobic edges. These vesicles called microsomes sediment at one hundred thousand times g, one hundred to three hundred nanometers diameter retaining orientation original membrane. Rough microsomes bear ribosomes and contain Sec61 translocon, oligosaccharyltransferase, BiP, permitting in vitro translation translocation assays that defined signal peptide cleavage and core glycosylation. Smooth microsomes derive from smooth ER and contain cytochrome P450, glucose-six-phosphatase and are inducible by drugs. Golgi fragments produce separate Golgi microsomes of different density, mitochondria when broken produce mitoplasts not microsomes, lysosomes release soluble hydrolases rather than resealing same way. Marker enzyme glucose-six-phosphatase and NADPH cytochrome c reductase enrich in microsomes, confirming ER origin. Their artificial nature useful for biochemical reconstitution but not physiological organelles. Integration with cell cycle kinases, calcium signaling and mechanical cues ensures coordinated remodeling during growth, migration and differentiation.

Ref: Palade Science 1975; microsomes ER fragments 100k g in vitro translation translocation Nobel work.