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Golgi apparatus
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Golgi Apparatus
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endomembrane system Semi-autonomous organelles Protein sorting to organelles Systems biology of cells Cell Biology & Cell Theory Cell biology: The study of individual cells and their interactions. Cell Theory (Schleiden & Schwann, with contributions from Virchow): All living organisms are composed of one or more cells. Cells are the smallest units of life. New cells arise only from pre-existing cells through division (e.g., binary fission). Origins of Life: Four Overlapping Stages Stage 1: Formation of Organic Molecules Primitive Earth conditions favored spontaneous organic molecule formation. Hypotheses on the origin of organic molecules: Reducing Atmosphere Hypothesis: Earth's early atmosphere (rich in water vapor) facilitated molecule formation. Stanley Miller’s experiment simulated early conditions, producing amino acids and sugars. Extraterrestrial Hypothesis: Organic carbon (amino acids, nucleic acid bases) may have come from meteorites. Debate exists over survival after intense heating. Deep-Sea Vent Hypothesis: Molecules formed in the temperature gradient between hot vent water & cold ocean water. Supported by experimental evidence. Alkaline hydrothermal vents may have created pH gradients that allowed organic molecule formation. Stage 2: Formation of Polymers Early belief: Prebiotic synthesis of polymers was unlikely in aqueous solutions (water competes with polymerization). Experimental evidence: Clay surfaces facilitated the formation of nucleic acid polymers and polysaccharides. Stage 3: Formation of Boundaries Protobionts: Aggregates of prebiotically produced molecules enclosed by membranes. Characteristics of a protobiont: Boundary separating the internal & external environments. Polymers with information (e.g., genetic material, metabolic instructions). Catalytic functions (enzymatic activities). Self-replication. Liposomes: Vesicles surrounded by lipid bilayers. Can enclose RNA and divide. Stage 4: RNA World Hypothesis RNA was likely the first macromolecule in protobionts due to its ability to: Store information. Self-replicate. Catalyze reactions (ribozymes). Chemical Selection & Evolution: RNA mutations allowed faster replication & self-sufficient nucleotide synthesis. Eventually, RNA world was replaced by the DNA-RNA-protein world due to: DNA providing more stable information storage. Proteins offering greater catalytic efficiency and specialized functions. Microscopy Microscopy Parameters Resolution: Ability to distinguish two adjacent objects. Contrast: Difference between structures (enhanced by special dyes). Magnification: Ratio of image size to actual size. Types of Microscopes Light Microscope: Uses light; resolution = 0.2 micrometers. Electron Microscope: Uses electron beams; resolution = 2 nanometers (100x better than light microscopes). Light Microscopy Subtypes Bright Field: Standard; light passes directly through. Phase Contrast: Amplifies differences in light phase shifts. Differential Interference Contrast (DIC): Enhances contrast for internal structures. Electron Microscopy Subtypes Transmission Electron Microscopy (TEM): Thin slices stained with heavy metals. Some electrons scatter while others pass through to create an image. Scanning Electron Microscopy (SEM): Heavy metal-coated sample. Electron beam scans the surface, producing 3D images. Cell Structure & Function Determined by matter, energy, organization, and information. Genome: The complete set of genetic material. Prokaryotic vs. Eukaryotic Cells Feature Prokaryotic Cells Eukaryotic Cells Nucleus ❌ Absent ✅ Present Membrane-bound organelles ❌ None ✅ Yes Size Small (1-10 µm) Large (10-100 µm) Examples Bacteria, Archaea Plants, Animals, Fungi, Protists Prokaryotic Cell Structure Plasma Membrane: Lipid bilayer barrier. Cytoplasm: Internal fluid. Nucleoid Region: DNA storage (no nucleus). Ribosomes: Protein synthesis. Cell Wall: (Some) Provides structure & protection. Glycocalyx: Protection & hydration. Flagella: Movement. Pili: Attachment. Eukaryotic Cell Structure Nucleus: Contains DNA & controls cell functions. Organelles: Rough ER: Protein synthesis & sorting. Smooth ER: Lipid synthesis, detoxification. Golgi Apparatus: Protein modification & sorting. Mitochondria: ATP production (Powerhouse of the Cell™). Lysosomes: Digestive enzymes for breakdown & recycling. Peroxisomes: Breakdown of harmful substances. Cytoskeleton: Provides structure (microtubules, actin filaments, intermediate filaments). Plasma Membrane: Regulates transport & signaling. Endomembrane System Includes: Nucleus, ER, Golgi apparatus, lysosomes, vacuoles, and plasma membrane. Nuclear Envelope: Double membrane structure. Nuclear pores allow molecule transport. Golgi Apparatus: Modifies & sorts proteins/lipids. Packages proteins into vesicles for secretion (exocytosis). Lysosomes: Contain acid hydrolases for macromolecule breakdown. Perform autophagy (organelle recycling). Semi-Autonomous Organelles Mitochondria Function: ATP production (cellular respiration). Structure: Outer & inner membrane (inner folds = cristae for increased surface area). Mitochondrial matrix houses metabolic enzymes. Chloroplasts (Plants & Algae) Function: Photosynthesis (light energy → chemical energy). Structure: Outer & inner membrane. Thylakoid membrane (site of photosynthesis). Contains chlorophyll. Endosymbiosis Theory Mitochondria & chloroplasts evolved from free-living bacteria that were engulfed by an ancestral eukaryotic cell. Protein Sorting & Cell Organization Co-translational sorting: Proteins destined for ER, Golgi, lysosomes, vacuoles, or secretion. Post-translational sorting: Proteins sent to nucleus, mitochondria, chloroplasts, peroxisomes. Systems Biology Studies how cellular components interact to form a functional system
Updated 34d ago
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Golgi apparatus
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golgi apparatus
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The Endoplasmic Reticulum (Er) Plays A Key Role In The Modification Osince The Rough Er Helps Modify Proteins That Will Be Secreted From The Cell, Cells Whose Job Is To Secrete Large Amounts Of Enzymes Or Other Proteins, Such As Liver Cells, Have Lots Of Rough Er. Smooth Er The Smooth Endoplasmic Reticulum (Smooth Er) Is Continuous With The Rough Er But Has Few Or No Ribosomes On Its Cytoplasmic Surface. Functions Of The Smooth Er Include: Synthesis Of Carbohydrates, Lipids, And Steroid Hormones Detoxification Of Medications And Poisons Storage Of Calcium Ions In Muscle Cells, A Special Type Of Smooth Er Called The Sarcoplasmic Reticulum Is Responsible For Storage Of Calcium Ions Which Are Needed To Trigger The Coordinated Contractions Of Muscle Fibers. There Are Also Tiny "Smooth" Patches Of Er Found Within The Rough Er. These Patches Serve As Exit Sites For Vesicles Budding Off From The Rough Er And Are Called Transitional Er . The Golgi Apparatus When Vesicles Bud Off From The Er, Where Do They Go? Before Reaching Their Final Destination, The Lipids And Proteins In The Transport Vesicles Need To Be Sorted, Packaged, And Tagged So That They Wind Up In The Right Place. This Sorting, Tagging, Packaging, And Distribution Takes Place In The Golgi Apparatus (Golgi Body), An Organelle Made Up Of Flattened Discs Of Membrane. Micrograph Of The Golgi Apparatus Showing A Series Of Flattened Membrane Discs In Cross-Section _image Credit: "The Endomembrane System And Proteins: Figure 3" By Openstax College, Biology (Cc By 3.0), Modification Of Work By Lousia Howard_ The Receiving Side Of The Golgi Apparatus Is Called The Cis Face And The Opposite Side Is Called The Trans Face. Transport Vesicles From The Er Travel To The Cis Face, Fuse With It, And Empty Their Contents Into The Lumen Of The Golgi Apparatus. As Proteins And Lipids Travel Through The Golgi, They Undergo Further Modifications. Short Chains Of Sugar Molecules Might Be Added Or Removed, Or Phosphate Groups Attached As Tags. Carbohydrate Processing Is Shown In The Diagram As The Gain And Loss Of Branches On The Purple Carbohydrate Group Attached To The Protein. Image Showing Transport Of A Membrane Protein From The Rough Er Through The Golgi To The Plasma Membrane. The Protein Is Initially Modified By The Addition Of Branching Carbohydrate Chains In The Rough Er; These Chains Are Then Trimmed Back And Replaced With Other Branching Chains In The Golgi Apparatus. The Protein, With Its Final Set Of Carbohydrate Chains, Is Then Transported To The Plasma Membrane In A Transport Vesicle. The Vesicle Fuses With The Plasma Membrane, Its Lipids And Protein Cargo Becoming Part Of The Plasma Membrane. _image Modified From "The Endomembrane System And Proteins: Figure 1" By Openstax College, Biology (Cc By 3.0), Modification Of Work By Magnus Manske_ Finally, The Modified Proteins Are Sorted (Based On Markers Such As Amino Acid Sequences And Chemical Tags) And Packaged Into Vesicles That Bud From The Trans Face Of The Golgi. Some Of These Vesicles Deliver Their Contents To Other Parts Of The Cell Where They Will Be Used, Such As The Lysosome Or Vacuole. Others Fuse With The Plasma Membrane, Delivering Membrane-Anchored Proteins That Function There And Releasing Secreted Proteins Outside The Cell. Cells That Secrete Many Proteins—Such As Salivary Gland Cells That Secrete Digestive Enzymes, Or Cells Of The Immune System That Secrete Antibodies—Have Many Golgi Stacks. In Plant Cells, The Golgi Apparatus Also Makes Polysaccharides (Long-Chain Carbohydrates), Some Of Which Are Incorporated Into The Cell Wall. Lysosomes The Lysosome Is An Organelle That Contains Digestive Enzymes And Acts As The Organelle-Recycling Facility Of An Animal Cell. It Breaks Down Old And Unnecessary Structures So Their Molecules Can Be Reused. Lysosomes Are Part Of The Endomembrane System, And Some Vesicles That Leave The Golgi Are Bound For The Lysosome. Lysosomes Can Also Digest Foreign Particles That Are Brought Into The Cell From Outside. As An Example, Let'S Consider A Class Of White Blood Cells Called Macrophages, Which Are Part Of The Human Immune System. In A Process Known As Phagocytosis, A Section Of The Macrophage’S Plasma Membrane Invaginates—Folds Inward—To Engulf A Pathogen, As Shown Below. Diagram Of Phagocytosis, In Which The Phagosome Generated By Engulfment Of A Particle Fuses With A Lysosome, Allowing Digestion Of The Particle. _image Credit: Modified From "The Endomembrane System And Proteins: Figure 4" By Openstax College, Biology (Cc By 3.0)_ The Invaginated Section, With The Pathogen Inside, Pinches Off From The Plasma Membrane To Form A Structure Called A Phagosome. The Phagosome Then Fuses With A Lysosome, Forming A Combined Compartment Where Digestive Enzymes Destroy The Pathogen. Vacuoles Plants Cells Are Unique Because They Have A Lysosome-Like Organelle Called The Vacuole. The Large Central Vacuole Stores Water And Wastes, Isolates Hazardous Materials, And Has Enzymes That Can Break Down Macromolecules And Cellular Components, Like Those Of A Lysosome. Plant Vacuoles Also Function In Water Balance And May Be Used To Store Compounds Such As Toxins And Pigments (Colored Particles). Lysosomes Vs. Peroxisomes One Point That Can Be Confusing Is The Difference Between Lysosomes And Peroxisomes. Both Types Of Organelles Are Involved In Breaking Down Molecules And Neutralizing Hazards To The Cell. Also, Both Usually Show Up As Small, Round Blobs In Diagrams. However, The Peroxisome Is A Different Organelle With Its Own Unique Properties And Role In The Cell. It Houses Enzymes Involved In Oxidation Reactions, Which Produce Hydrogen Peroxide ( ) As A By-Product. The Enzymes Break Down Fatty Acids And Amino Acids, And They Also Detoxify Some Substances That Enter The Body. For Example, Alcohol Is Detoxified By Peroxisomes Found In Liver Cells. Importantly, Peroxisomes—Unlike Lysosomes—Are Not Part Of The Endomembrane System. That Means They Don'T Receive Vesicles From The Golgi Apparatus. You Can Learn More About How Proteins Are Shipped To The Peroxisome In The Article On Protein Targeting.F Proteins And The Synthesis Of Lipids. It Consists Of A Network Of Membranous Tubules And Flattened Sacs. The Discs And Tubules Of The Er Are Hollow, And The Space Inside Is Called The Lumen. Rough Er The Rough Endoplasmic Reticulum (Rough Er) Gets Its Name From The Bumpy Ribosomes Attached To Its Cytoplasmic Surface. As These Ribosomes Make Proteins, They Feed The Newly Forming Protein Chains Into The Lumen. Some Are Transferred Fully Into The Er And Float Inside, While Others Are Anchored In The Membrane. Inside The Er, The Proteins Fold And Undergo Modifications, Such As The Addition Of Carbohydrate Side Chains. These Modified Proteins Will Be Incorporated Into Cellular Membranes—The Membrane Of The Er Or Those Of Other Organelles—Or Secreted From The Cell. If The Modified Proteins Are Not Destined To Stay In The Er, They Will Be Packaged Into Vesicles, Or Small Spheres Of Membrane That Are Used For Transport, And Shipped To The Golgi Apparatus. The Rough Er Also Makes Phospholipids For Other Cellular Membranes, Which Are Transported When The Vesicle Forms.
Updated 259d ago
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Golgi apparatus
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