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Ch. 6 and 7 (Nucleus (Ribosomes (Endomembrane System (Endoplasmic…
Ch. 6 and 7
Nucleus
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At the lip of each pore, the inner and outer membranes of the nuclear envelope are continuous.
An intricate protein structure called a pore complex lines each pore and plays a role in the cell by regulating the entry and exit of proteins and RNAs.
Except at the pores, the nuclear side of the envelope is lined by the nuclear lamina, a net like array of protein filaments that maintains the shape of the nucleus by mechanically supporting the nuclear envelope.
Within the nucleus, the DNA is organized into discrete units called chromosomes, structures that carry the genetic information.
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When a cell is not dividing, stained chromatin appear as a diffuse mass and the chromosomes cannot be distinguished.
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In the nucleolus, proteins imported from the cytoplasm are assembled with the rRNA into subunits of ribosomes.
The subunits exit the nucleus through the nuclear pores to the cytoplasm, where a subunit can assemble into a ribosome.
Ribosomes
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Cells that have high rates of protein synthesis have large numbers of ribosomes as well as prominent nucleoli.
Free ribosomes are in the cytosol, while bound ribosomes are attached to the outside of the endoplasmic reticulum or nuclear envelope.
Proteins made on free ribosomes function within the cytosol and bound ribosomes make proteins that are destined for insertion into membranes for packaging with certain organelles.
Endomembrane System
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The system carries out a variety of tasks including synthesis of proteins, transport of proteins, metabolism and movement of lipids and detoxification of poisons.
The membranes of this system are related either through direct physical continuity or by the transfer of membrane segments as tiny vesicles, or sacs made of membrane.
Endoplasmic Reticulum
The endoplasmic reticulum (ER) is an extensive network of membranes that accounts for more than half of the total membrane in eukaryotic cells.
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The ER membrane separates the internal compartment of the ER, called the ER lumen.
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Enzymes of the ER are important in the synthesis of lipids, including oils.
Other enzymes of the smooth ER help detoxify drugs and poisons, especially in the liver.
The smooth ER stores calcium ions. For example, in the muses it pumps calcium ions from the cytosol into the ER lumen.
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Most secretory proteins are glycoproteins, proteins with carbohydrates covalently bonded to them.
After security proteins are formed, the ER membrane keeps them separate from proteins in the cytosol and produced by free ribosomes.
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Golgi Apparatus
After leaving the ER, many transport vesicles travel to the Golgi apparatus.
Products of the ER, such as proteins, are modified and stored and then sent to other destinations.
It consists of flattened membranous sacs, cisternae, looking like a stack of pita bread.
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Vesicle in the Golgi apparatus are engaged in the transfer of material between parts of the Golgi and other structures.
A Golgi stack has a distinct structural directionality, with the membranes of cisternae on opposite sides of the stack differing in thickness and molecular composition.
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A vesicle that buds from the ER can add its membrane and the contents of its lumen to the cis face by fusing with a Golgi membrane on that side.
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Lysosomes
Lysosome is a membranous say of hydrolytic enzymes that many eukaryotic cells use to digest macromolecules.
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If a lysosome breaks open or leaks, the released enzymes are not very active because the cytosol has a near-neutral pH.
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Amoebas and many other unicellular eukaryotes eat by engulfing smaller organisms or food particles by phagocytosis.
The food vacuole formed fuses with a lysosome, whose enzymes digest the food.
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Digestion products, including simple sugars, amino acids and other monomers, pass into the cytosol and become nutrients.
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In autophagy, a damaged organelle or small amount of cytosol becomes surrounded by a double membrane and a lysosome fuses with the outer membrane of this vesicle.
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Vacuoles
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Many unicellular eukaryotes living in fresh water have contractile vacuoles that pump water out of the cell, maintaining a concentration of ions and molecules inside the cell.
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The central vacuole plays a role in he growth of plant cells, which enlarge as a vacuole absorbs water, enabling the cell to become larger with a minimal investment in new cytoplasm.
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Microscopy
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Light microscope (LM) is visible light that passes through the specimen and then through glass lenses.
The lenses bend the light in a way that the image of the specimen is magnifies as it is projected into the eye or into a camera.
Magnification is the ratio of an object's image size to its real size. LM can magnify 1,000 times the actuations size.
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Until recently, the resolution barrier prevented cell biologists from using LM when studying organelles or the membrane-enclosed structures within eukaryotic cells.
In the 1950s, the electron microscope (EM) was introduced and it focuses on the beams of electrons through the specimen or into its surface.
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Microscopes are important tools for cytology, the study of cell structure.
Cell Fractionation
Cell fractionation takes cells apart and separates major organelles and other subcellular structures from one another.
The piece of equipment that is used for this tasks is the centrifuge, it spins test tubes holding mixtures of disrupted cells at a series of increasing speeds.
At each speed, the resulting force causes a subset of the cell components to settle to the bottom of the tube.
At low speeds the pellet consists of large components, and higher speeds result in a pellet with smaller components.
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Lipids and Proteins
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A phospholipid is an amphipathic molecule, meaning it has both hydrophobic and hydrophilic regions.
A phospholipid bilayer can exist as a stable boundary between two aqueous compartments because the molecular arrangement shelters the hydrophobic taels of the phospholipids from water while exposing the hydrophilic heads to water.
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In the fluid mosaic model, the membrane is a mosaic of protein molecules bobbing in a fluid bilayer of phospholipids.
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Fluidity of Membranes
A membrane is held together by hydrophobic interactions, which are weaker than covalent bonds.
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Some membrane proteins seem to move in a highly directed manner, perhaps along cytoskeletal fibers in the cell by motor proteins connected to the membrane proteins' cytoplasmic regions.
A membrane remains fluid as temperature decreases until the phospholipids settle into a closely packed arrangement and the membrane solidifies.
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As the temperature decreases, the membrane remains fluid to a lower temperature if its rich in phospholipids with unsaturated hydrocarbon tails.
Due to kinks in the tails where double bonds are located, unsaturated hydrocarbon tails cannot pack closely as saturated hydrocarbon tails making the membrane more fluid.
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