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Kompartemen intraseluler Regulasi PROTEIN pascatranslasi
SISTEM ENDOMEMBRAN Kompartemen intraseluler Regulasi PROTEIN pascatranslasi
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Components of the endomembrane system:
Concept 6.4: The endomembrane system regulates protein traffic and performs metabolic functions in the cell Components of the endomembrane system: Nuclear envelope Endoplasmic reticulum Golgi apparatus Lysosomes Vacuoles Plasma membrane These components are either continuous or connected via transfer by vesicles Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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Nuclear envelope
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The Endoplasmic Reticulum: Biosynthetic Factory
The endoplasmic reticulum (ER) accounts for more than half of the total membrane in many eukaryotic cells The ER membrane is continuous with the nuclear envelope There are two distinct regions of ER: Smooth ER, which lacks ribosomes Rough ER, with ribosomes studding its surface For the Cell Biology Video ER and Mitochondria in Leaf Cells, go to Animation and Video Files. Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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Smooth ER Nuclear envelope Rough ER ER lumen Cisternae Transitional ER
Fig. 6-12 Smooth ER Nuclear envelope Rough ER ER lumen Cisternae Transitional ER Ribosomes Transport vesicle 200 nm Smooth ER Rough ER Figure 6.12 Endoplasmic reticulum (ER)
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Functions of Smooth ER The smooth ER Synthesizes lipids
Metabolizes carbohydrates Detoxifies poison Stores calcium Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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Functions of Rough ER The rough ER
Has bound ribosomes, which secrete glycoproteins (proteins covalently bonded to carbohydrates) Distributes transport vesicles, proteins surrounded by membranes Is a membrane factory for the cell Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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The Golgi Apparatus: Shipping and Receiving Center
The Golgi apparatus consists of flattened membranous sacs called cisternae Functions of the Golgi apparatus: Modifies products of the ER Manufactures certain macromolecules Sorts and packages materials into transport vesicles For the Cell Biology Video ER to Golgi Traffic, go to Animation and Video Files. For the Cell Biology Video Golgi Complex in 3D, go to Animation and Video Files. For the Cell Biology Video Secretion From the Golgi, go to Animation and Video Files. Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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(“receiving” side of Golgi apparatus) 0.1 µm
Fig. 6-13 cis face (“receiving” side of Golgi apparatus) 0.1 µm Cisternae Figure 6.13 The Golgi apparatus trans face (“shipping” side of Golgi apparatus) TEM of Golgi apparatus
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Lysosomes: Digestive Compartments
A lysosome is a membranous sac of hydrolytic enzymes that can digest macromolecules Lysosomal enzymes can hydrolyze proteins, fats, polysaccharides, and nucleic acids Animation: Lysosome Formation Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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A lysosome fuses with the food vacuole and digests the molecules
Some types of cell can engulf another cell by phagocytosis; this forms a food vacuole A lysosome fuses with the food vacuole and digests the molecules Lysosomes also use enzymes to recycle the cell’s own organelles and macromolecules, a process called autophagy For the Cell Biology Video Phagocytosis in Action, go to Animation and Video Files. Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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Fig. 6-14 Nucleus 1 µm Vesicle containing two damaged organelles 1 µm Mitochondrion fragment Peroxisome fragment Lysosome Digestive enzymes Lysosome Lysosome Plasma membrane Peroxisome Figure 6.14a Lysosomes Digestion Food vacuole Mitochondrion Digestion Vesicle (a) Phagocytosis (b) Autophagy
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Vacuoles: Diverse Maintenance Compartments
A plant cell or fungal cell may have one or several vacuoles Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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Video: Paramecium Vacuole
Food vacuoles are formed by phagocytosis Contractile vacuoles, found in many freshwater protists, pump excess water out of cells Central vacuoles, found in many mature plant cells, hold organic compounds and water Video: Paramecium Vacuole Copyright © 2008 Pearson Education, Inc., publishing as Pearson Benjamin Cummings
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Central vacuole Cytosol Nucleus Central vacuole Cell wall Chloroplast
Fig. 6-15 Central vacuole Cytosol Nucleus Central vacuole Figure 6.15 The plant cell vacuole Cell wall Chloroplast 5 µm
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Kompartemen intraseluler Regulasi PROTEIN pascatranslasi
SISTEM ENDOMEMBRAN Kompartemen intraseluler Regulasi PROTEIN pascatranslasi
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Polyribosomes A number of ribosomes can translate a single mRNA simultaneously, forming a polyribosome (or polysome) Polyribosomes enable a cell to make many copies of a polypeptide very quickly Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Completed polypeptide Growing polypeptides Incoming ribosomal subunits
Fig Completed polypeptide Growing polypeptides Incoming ribosomal subunits Polyribosome Start of mRNA (5 end) End of mRNA (3 end) (a) Ribosomes Figure Polyribosomes mRNA (b) 0.1 µm
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Completing and Targeting the Functional Protein
Often translation is not sufficient to make a functional protein Polypeptide chains are modified after translation Completed proteins are targeted to specific sites in the cell Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Protein Folding and Post-Translational Modifications
During and after synthesis, a polypeptide chain spontaneously coils and folds into its three-dimensional (3D) shape Proteins may also require post-translational modifications before doing their job Some polypeptides are activated by enzymes that cleave them Other polypeptides come together to form the subunits of a protein Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Protein Folding Figure 6–84 Co-translational protein folding.
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Protein Folding Figure 6–86 The Hsp70 family of molecular chaperones.
Figure 6–87 The structure and function of the Hsp60 family of molecular chaperones.
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Targeting Polypeptides to Specific Locations
Two populations of ribosomes are evident in cells: free ribsomes (in the cytosol) and bound ribosomes (attached to the ER) Free ribosomes mostly synthesize proteins that function in the cytosol Bound ribosomes make proteins of the endomembrane system and proteins that are secreted from the cell Ribosomes are identical and can switch from free to bound Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Polypeptide synthesis always begins in the cytosol
Synthesis finishes in the cytosol unless the polypeptide signals the ribosome to attach to the ER Polypeptides destined for the ER or for secretion are marked by a signal peptide A signal-recognition particle (SRP) binds to the signal peptide The SRP brings the signal peptide and its ribosome to the ER Copyright © 2008 Pearson Education Inc., publishing as Pearson Benjamin Cummings
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Ribosome mRNA Signal peptide ER membrane Signal peptide removed
recognition particle (SRP) Protein CYTOSOL Translocation complex ER LUMEN SRP receptor protein Sintesis protein pada REK: Translasi protein berawal di sitosol. Peptida sinyal (20-25 residu AA hidrofobik pada N-terminal) diikat oleh SRP. SRP berikatan dengan reseptor RSP (protein penambat/docking protein) yang ada di membran REK, menambatkan ribosom ke REK. SRP dilepaskan dan sintesis protein dilanjutkan. Polipeptida mengalami elongasi (nascent polypeptide) masuk ke dalam lumen REK dan peptida sinyal dilepaskan. Sintesis protein selesai, nascent polypeptide dilepaskan ke lumen REK, unit translasi terdisosiasi. Figure The signal mechanism for targeting proteins to the ER
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Overview: Protein trafficking
Nucleus Rough ER Smooth ER cis Golgi Figure 6.16 Review: relationships among organelles of the endomembrane system Plasma membrane trans Golgi
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Modifikasi protein pada Retikulum Endoplasma
Penambahan gugus fungsional tertentu pada protein. Figure 6–82 Steps in the creation of a functional protein.
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To be continue… Take home activity
Modifikasi protein pada RE Sortasi protein sekresi pada apparatus Golgi PPT print 6 slides/page; references
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