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Lecture 10

Golgi complex

QuestionAnswer
Camillo Golgi who first described its existence in the late 1800's
Golgi apparatus involved with processing and packaging of protein products for secretion or passage t other organelles
Golgi Stack 3-8 series of cisternae; flat disc-like membranous sacs
Intracisternal space the lumen of the golgi cisternae
Golgi has 2 sides cis or forming face and trans or maturing face
Cis-golgi network CGN oriented towards the RER receives transition vesicles from the RER
Trans-golgi network TGN the opposite side from it transport vesicles carry processed proteins and lipids to: secrectory granules,endosomes, lysosomes,plasma memebrane
medial cisternae are all of the golgi cisternae between the cis and trans faces
Material Flow through the Golgi 2 models 1. stationary Model 2. maturation model
stationary model 1. each layer is stable 2. shuttle vesicles carry the contents from one layer to the next
maturation model 1. each cisterna is only transiently positioned in one layer 2. each cisterna moves from one layer to the next 3. each cisternae originates initially as the CGN then as more transition vesicles fuse above it, it becomes part of the medical cisternae 4.
if the maturation model is true then how do the processing enzymes of the CGN stay in the first cisternae? retragade transport back to CGN from the medial cisternae via shuttle vesicles
Golgi function 1. most materials move from the CGN towaards the TGN 2. some materials can move in the opposite direction aka. retrograde transport
retrograde transport assures that each level of the golgi maintains specific compartments with specific proteins, which occurs via specific protein sequence tags that designate the proteins for return
golgi proteins 1. with shorter transmembrane domains are found towards the CGN 2. with longer transmembrane domains are found in the TGN
transport vesicles are vesicles that form from the TGN
transport vesicles have 3 fates 1. give rise to secretory vesicles 2. give rise to early endosomes, contain lysosomal hydrolases-digestive enzymes 3. retrograde transport
protein modification in the RER initial glycosylation maily N-linked to asparagine
protein modification in the golgi 1. further glycosylation mainly O-linked to serine and threonine 2. modification of both N and O linked glycosylation. 3. protein tyrosine sulfation
Protein sorting 1. various proteins must be designated for specific cellular compartments 2. involve specific sequence tags or specific glycosylation
example of protein sorting targeting of soluble proteins for lysosomes
secretory pathways of protein sorting 1. constitutive secretion 2. regulated secretion
constitutive secretion (continuous secretion) specific protein sequence tags target proteins for continuous secretion
regulated secretion other specific protein sequence tags target proteins for regulated secretion
membrane polarity onset of polarity begins at the ER and continues through the golgi, to the plasma membrane and other organelles
protein glycosylation and sulfation occur in the RER and golgi lumen
specific example of a protein destined for the regulated secretion pathway GLUT4
GLUT4 glucose transporter associated with the facilitated diffusion of glucose into cells import role in regulating glucose balance
GLUT4 1.one of 13 sugar transporter proteins contains 12-transmembrane domains 2. insulin sensitive 3. synthesized in RER 4. a single site of N-glycosylation
GLUT4 Trafficking 1. glut4 is packaged into transport vesicle at the TGN 2. GLUT4 are then directed to the cell membrane where they are docked to the membrane 3. insulin signaling causes them to fuse to the membrane 4. the GLUT4 tansporters can be recycled to endosomes
Created by: aareynolds
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