Inclusions
1. ORGANELLES:
ribosomes, endoplasmic
reticulum, golgi apparatus,
lysosomes, peroxisomes,
proteasomes,
mitochondria,
cytoskeleton
2. INCLUSSION: glycogen,
lipid, pigment, crystals
Organelles
metabolically active cellular structure that execute spesific
functions
Detoxification toxic
material
- Glycogen Metabolism
Calsium reservoir SR
Ribosomes
Small particle Conglomeration of mRNA-
Large subunit and small ribosome complex
subunit polysomes
Protein and rRNA
Small unit : binding mRNA,
peptidyl tRNA, aminoacyl Free ribosome : syntesize
tRNA cytosolic prot, peripheral
Large subunit: ribozyme membrane prot, prot
2 type : Free ribosomes destine for nucl, mit,
and membrane associated peroxisome
ribosomes
Rough ER (RER)
- Interconnected tubules and vesicles
- Ribosomes
- Synthesized :
a. Integral protein of plasma membrane, ER, Golgi
complex, and lysosomal proteins
b. Protein to be secreted from the cell
c. Protein that has to be packages or modified
Related to :
1. Polyribosomes & Free Ribosomes
2. Messenger RNA (mRNA)
3. Transfer RNA (tRNA)
- Perform initial post-translation modification
c. Membrane lipid (phospholipid)
The endoplasmic reticulum
3-10
Rough ER (RER)
Signal recognition
particle receptor
(docking protein)
Ribosome receptor
protein (ribophorin
I dan ribophorin II)
Pore protein
(translocator)
Golgi Apparatus
Structure :
- Membrane-bounded Cisternae Golgi Stack
Function:
- Synthesis of carbohydrates
- Modification of proteins manufactured on RER
- Sorting of proteins manufactured on RER
Vesicle target membrane
SNARE protein (soluble attachment receptor
N-ethylmaleimide sensitive fusion protein)
SNARE rich region porosomes
Rabs GTPases specializing in target
recognition
Coated protein : COP and clathrin
Marker microtubule for transported
Vesicles from TGN:
1. Constitutive secretory
pathway
- Insert in to cell membrane
- Fuse with the cell
membrane
2. Regulated secretory
pathway
- Secretory granule
- Fuse with late endosome
lysosome
Lysosomes
Polymorphous in shape;
: 0,3-0,8 m; 40 acid
hydrolases
Digesting : macromol,
phagocytosed mo, cell
debris, excess/senescent
organelle
Formation : vesicle from
TGN fuse with late
endosomes lysosomes
3 ways : phagosomes,
autophagosomes, reseptor
mediated pinocytic ves.
Hereditary enzyme deficiency
Disease Enzyme deficiency
Hurler Iduronidase
Hunter syndrome Iduronat sulfatase
Crabbe -galactosidase
Tay-Sachs Hexsosaminidase
Gaucher -glucosidase/
glukoserebrosidase
Fabry a-galactosidase
Pompe a-glucosidase
Mitochondria
- Rod-shaped organelles
- Outer membrane
- Intermembrane space
- Matrix
Outer membrane
Protein : lipid- 1:1
Porin
Relative permeable
Inner Membrane
- 50 % protein
- Degradation of fatty
acids and pyruvate
acetyl CoA
TCA cycle (Krebs cycle)
- Ribosomes, tRNA,
mRNA, cDNA and matrix
granules
Contact sites
Outer and inner membrane
mit. Contact each other
3-27
Proteasomes
- Barrel-shaped structure with
2 chamber, non membrane
bound
- Composed of protein
complexesproteolytic
enzyme
- Function : degradation
malformed protein, cleaved
antigenic protein into epitop
Proteolytic pathway must able to distinguish
between completed protein that have wrong
conformation and many growing polypeptides on
ribosomes that have not yet achieved their normal
folded conformation
- Involved 3 enzymes :
Ubiquitin-activating enz,
ubiquitin-conjugating enz,
ubiquitin ligases
Peroxisomes
Microbodies , small, 0,2-1 m,
Membrane bound
Oxidative enzymes ( 40)
Function :
- Catabolism of long chain fatty acid via
oxidation acetyl group cytosol
syntesize of cholesterol
- Formation hydrogen peroxide (H2O2)
excess-- catalase
Inclusions
Non living component of the cells
Not possed metabolic activity
Not bounded by membranes