Cell Biology: Cell Membrane, Cytoskeleton, Organelles, and Endomembrane System

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Vocabulary practice flashcards covering cell membrane dynamics, cytoskeletal structures, cytoplasmic inclusions, mitochondria, peroxisomes, and the endomembrane system based on the provided biology lecture notes.

Last updated 7:38 AM on 9/29/26
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26 Terms

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Fluid Mosaic Model

A structural model proposed by Singer and Nicholson describing the plasma membrane as a dynamic lipid bilayer where embedded proteins move laterally in a mosaic-like arrangement.

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Flip-Flop Movement

The transverse diffusion process in which a lipid molecule flips from one monolayer (leaflet) of the membrane bilayer to the opposite monolayer.

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Lipid Rafts

Denser microdomains of the cell membrane enriched in cholesterol and sphingolipids that move laterally and participate in cell signaling, cell movement, and endocytosis.

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Glycocalyx

A sugar-rich coat on the outer surface of the plasma membrane composed of glycoproteins, glycolipids, and proteoglycans that functions in cell protection, recognition, and adhesion.

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<p>Coupled Transport Modes</p>

Coupled Transport Modes

Transporter mechanisms classified by cargo direction: uniport (single molecule), symport (co-transport of two molecules in the same direction), and antiport (transport of two molecules in opposite directions).

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Na+/K+\text{Na}^+/\text{K}^+ Pump

An ATPase-mediated antiport pump that uses 1 ATP1\,\text{ATP} to pump 3 Na+3\,\text{Na}^+ ions out of the cell and 2 K+2\,\text{K}^+ ions into the cell, maintaining cell volume and membrane potential.

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Caveolae

Bulb-shaped invaginations (50 nm50\,\text{nm}) of the plasma membrane formed by caveolin dimers that represent a specialized form of lipid raft involved in micropinocytosis.

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<p>Anterograde Transport</p>

Anterograde Transport

Vesicular movement of proteins and lipids forward from the rough endoplasmic reticulum to the Golgi apparatus and between Golgi cisternae via COP-II coated vesicles.

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Transcytosis

The intracellular transport of molecules from one extracellular space to another through sequential endocytosis and exocytosis, such as the transport of IgA dimers across epithelial cells.

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Hyaloplasm

The watery matrix or cytosol of the cytoplasm containing water-soluble salts, metabolites, enzymes, and signaling molecules.

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<p>Microtubule Structure</p>

Microtubule Structure

A hollow cylindrical cytoskeletal filament with a diameter of 20–25 nm20\text{--}25\,\text{nm} composed of 1313 parallel protofilaments formed by repeating α/β\alpha/\beta-tubulin heterodimers.

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<p>Kinesin and Dynein Motor Proteins</p>

Kinesin and Dynein Motor Proteins

Microtubule motor proteins that use ATP-derived energy to transport cargoes along microtubules: kinesin moves toward the plus end, whereas dynein moves toward the minus end.

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Axoneme

The structural cytoskeletal core of motile cilia and flagella consisting of 99 peripheral microtubule doublets surrounding 22 central microtubule singlets (9+29+2 pattern).

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<p>Intermediate Filaments</p>

Intermediate Filaments

Non-polar, stable cytoskeletal fibers (8–12 nm8\text{--}12\,\text{nm} in diameter) composed of fibrous proteins (such as keratins, vimentins, and lamins) that provide mechanical strength to cells.

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G-Actin

The globular monomeric subunit of actin that polymerizes into a double-helical polymer known as F-actin to form flexible microfilaments (6–8 nm6\text{--}8\,\text{nm} in diameter).

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Lipofuscin

Granular, electron-dense brown cytoplasmic inclusions composed of undigested lipid residues and cell debris that accumulate with age in quiescent cells like neurons and heart muscle.

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Cardiolipin

A unique phospholipid containing four fatty acid tails located in the inner mitochondrial membrane that lowers ion permeability and supports oxidative phosphorylation.

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<p>Electron Transport Chain</p>

Electron Transport Chain

A series of four enzyme complexes (I--IV) located in the inner mitochondrial membrane that transfer electrons and pump protons (H+\text{H}^+) into the intermembrane space to generate a proton gradient.

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Peroxisome

A single-membrane organelle containing catalase to break down hydrogen peroxide (H2O2\text{H}_2\text{O}_2) and enzymes responsible for the β\beta-oxidation of very long-chain fatty acids.

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KDEL Signal Sequence

A specific four-amino-acid sequence (Lys-Asp-Glu-Leu) located at the carboxyl terminus of proteins that retains them as resident proteins in the lumen of the endoplasmic reticulum.

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ERAD System

Endoplasmic Reticulum Associated Degradation; a quality control mechanism where chaperones detect misfolded proteins in the RER lumen and export them to the cytosol for proteasomal degradation.

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Dictyosome

A structural stack of 4–64\text{--}6 flattened membranous cisternae that forms the core unit of the Golgi apparatus.

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Acid Hydrolases

A group of hydrolytic enzymes (including proteases, nucleases, and lipases) housed within lysosomes that degrade macromolecules optimally at an acidic internal pH<5.0\text{pH} < 5.0.

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<p>Proteasome</p>

Proteasome

A barrel-shaped non-membranous protein complex composed of a 19S19\text{S} regulatory particle and a 20S20\text{S} core particle that degrades misfolded or tagged proteins.

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<p>Lys48 Polyubiquitination</p>

Lys48 Polyubiquitination

A specific polyubiquitination linkage pattern on target proteins that serves as the explicit signal for recognition and degradation by the proteasome.

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Autophagy

A lysosome-dependent catabolic pathway where double-membrane vesicles (autophagosomes) sequester damaged cellular components or organelles and fuse with lysosomes for degradation and recycling.