Chapter 1-7: Cellular Organelles and Membrane Structure (Vocabulary Flashcards)

Semi-autonomous organelles: mitochondria and chloroplasts

  • These two organelles are described as semi-autonomous: partly independent, functioning a bit like their own units within the cell.

  • They each contain their own distinct genetic information: a mitochondrial genome (distinct chromosome) and a chloroplast genome (distinct chromosome).

  • They cannot survive in isolation outside the cell; they rely on the rest of the cell for materials, but they operate somewhat independently in providing energy-related functions.

  • The space between their membranes is called the intermembrane space.

  • Chloroplasts feature an inner membrane folded into thylakoid membranes; stacked thylakoids form grana, and the space inside the thylakoids is the thylakoid lumen. These membrane structures optimize energy-transforming reactions in photosynthesis.

  • Mitochondria also have extensive inner membrane folding (cristae) to increase membrane surface area for energy transformation.

  • In both organelles, the elaborate membrane architecture increases workspace for energy transformation processes, enabling efficient production and storage of energy.

Photosynthesis and energy transformation in chloroplasts vs mitochondria

  • Chloroplasts: use light energy to build nutrient molecules (photosynthesis). The process captures light energy and converts it into chemical energy stored in organic molecules.

  • Mitochondria: break down organic nutrients to release energy stored as ATP to power cellular work (cellular respiration).

  • Plant cells contain chloroplasts as well as mitochondria; animal cells contain mitochondria but not chloroplasts.

  • The chloroplast builds nutrients; the mitochondrion provides usable energy by converting nutrients to ATP for cellular work.

Structure-focused overview: chloroplasts and mitochondria

  • Chloroplast structure:

    • Outer membrane

    • Intermembrane space

    • Inner membrane

    • Internal membranes: thylakoid membranes, which stack into grana; thylakoid lumen is the space inside the thylakoids

  • Mitochondria structure:

    • Outer membrane

    • Intermembrane space

    • Inner membrane (folded into cristae) to increase surface area and house energy-transforming machinery

  • In both organelles, the elaborate internal membrane geometry increases surface area to host enzymes and complexes required for energy transformations.

Endosymbiosis theory and organelle origins

  • Endosymbiosis theory describes how mitochondria and chloroplasts originated:

    • Mitochondria arose from ancestral proteobacteria.

    • Chloroplasts arose from ancestral cyanobacteria.

    • An ancestral eukaryotic cell engulfed a prokaryotic cell; rather than digesting it, a mutualistic relationship formed and evolved into modern organelles.

  • Key evidence for endosymbiosis:

    • Organelles have their own circular genomes resembling prokaryotic chromosomes.

    • Organelles possess ribosomes similar to prokaryotic ribosomes.

    • They replicate by a process similar to bacterial binary fission.

  • Ancestors have modern relatives: proteobacteria (mitochondria) and cyanobacteria (chloroplasts).

  • The genetic content of organelle genomes is small but essential for energy-transformation functions.

Genome and replication features in mitochondria and chloroplasts

  • Both organelles contain their own circular DNA molecules, resembling bacterial chromosomes, rather than the linear multiple chromosomes found in the eukaryotic nucleus.

  • Nuclear chromosomes in eukaryotes are linear and multiple; mitochondrial and chloroplast genomes are typically circular and singular in each organelle.

  • Both organelles have their own ribosomes, which resemble prokaryotic ribosomes rather than eukaryotic cytosolic ribosomes.

  • They grow and divide independently, using binary fission-like processes similar to bacteria.

  • The presence of their own genetic material and ribosomes supports their semi-autonomous status.

Protein sorting and targeting: co-translational vs post-translational

  • Protein sorting is essential to deliver proteins to the correct cellular location.

  • Co-translational sorting:

    • Sorting occurs concurrently with translation.

    • Signal sequences, typically at the N-terminus, direct ribosome–nascent chain complexes to the rough endoplasmic reticulum (ER).

    • Proteins entering the ER are packaged into vesicles, transported to the Golgi, processed, sorted, and then directed to lysosomes/vacuoles, plasma membrane, or for secretion.

  • Post-translational sorting:

    • Proteins are fully synthesized in the cytosol and then imported into target organelles (nucleus, mitochondria, chloroplasts, peroxisomes).

    • Targeting signals on the fully folded protein are recognized and facilitate import.

  • If a protein lacks any targeting signal, it remains in the cytosol.

  • This dual sorting system ensures proteins reach their proper cellular destinations.

Extracellular matrix (ECM) and cell interactions in animals

  • ECM components fall into two main protein categories:

    • Adhesive proteins: sticky, responsible for binding and anchoring ECM components to each other and to cells; they help hold the matrix together and connect the matrix to cells.

    • Structural proteins: provide strength and resilience to tissues, helping absorb and distribute mechanical forces.

  • ECM also contains carbohydrates, especially polysaccharides attached to proteins:

    • Glycosaminoglycans (GAGs): long, unbranched polysaccharides with strong negative charges.

    • Proteoglycans: core protein with covalently attached GAG chains.

  • The assembly of GAGs and proteoglycans creates a hydrated, water-rich cushion that resists compression due to the negative charges attracting water molecules, forming a protective gel-like ECM.

  • Visual: the ECM encloses a sheet of cells; proteins (yellow with brown stripes) and carbohydrate-rich proteoglycans (green chains with a purple core) form a hydrated matrix around cells.

Plant cell walls vs animal ECM: structural differences

  • Plant cells surround themselves with a rigid cell wall, in contrast to the more flexible ECM of animal cells.

  • Cell wall layers:

    • Primary cell wall: flexible to allow growth and expansion.

    • Secondary cell wall: thicker, sturdier, and more fixed once growth ceases.

  • Construction sequence:

    • The plant cell first builds the primary cell wall (cellulose-rich and flexible).

    • As growth slows, it deposits the secondary cell wall in between the primary wall and the plasma membrane, resulting in layered cellulose fibers.

    • Cellulose fibers are oriented in different directions across layers to maximize strength in multiple directions.

Review: big-picture study tool and cellular systems

  • A suggested study technique is to create big comparison tables (e.g., bacteria vs plant vs animal cells) to organize features, presence/absence, and functions.

  • A conceptual view: cells function as integrated systems consisting of major components that coordinate to maintain life processes.

  • The discussion sets the stage for continuing into Chapter 5, focusing on the cell membrane in more detail.

The cell membrane: structure, model, and function

  • Core structural foundations:

    • Phospholipid bilayer: essential building block; without it, membranes cannot form.

    • Proteins: numerous and essential for membrane function; they provide most membrane-specific activities.

    • Cholesterol: present in animal membranes, a steroid lipid with a four-ring structure; modulates membrane properties.

    • Carbohydrates: present as glycolipids and glycoproteins on the outer surface, contributing to cell recognition and signaling.

  • Major membrane components:

    • Phospholipids: amphipathic molecules with hydrophobic tails and a hydrophilic head; they form bilayers with two leaflets.

    • Proteins: embedded or associated with the bilayer; provide transport, signaling, enzymes, and structural roles.

    • Cholesterol: intercalates within the bilayer, influencing fluidity and rigidity.

    • Carbohydrates: attached to lipids (glycolipids) or proteins (glycoproteins) on the extracellular surface.

  • Phospholipids and leaflet asymmetry:

    • Two leaflets (inner cytosolic face and outer extracellular face) are not identical in composition.

    • Specific phospholipids predominate on the inner vs. outer leaflet, contributing to membrane organization and function.

  • The Singer–Nicolson fluid mosaic model:

    • The membrane is a mosaic of components that move laterally within the plane of the membrane.

    • The membrane is semi-fluid: lipids and proteins diffuse laterally but do not typically flip-flop across the bilayer without enzymatic help.

    • The model explains dynamic organization and function of membranes.

  • Membrane proteins: three major structural categories

    • Transmembrane proteins: span the entire bilayer, with hydrophobic regions in the membrane core and hydrophilic regions exposed to aqueous environments; stability requires hydrophobic residues in membrane-spanning segments.

    • Lipid-anchored proteins: proteins covalently linked to lipid molecules anchored in the membrane.

    • Peripheral proteins: non-covalently attached to the membrane surface or to other membrane proteins.

    • All transmembrane and lipid-anchored proteins are often considered integral membrane proteins because they have a portion embedded in the lipid bilayer.

  • The concept of membrane organization and protein attachment: clustering, anchoring, and functional localization.

Membrane fluidity and how cells regulate it

  • Membranes are semi-fluid and two-dimensional in-plane movement occurs, but molecules do not readily flip-flop between leaflets without enzymes (flipases).

  • Lipid rafts: microdomains—clusters of lipids that move together within the membrane plane, contributing to local organization and protein recruitment.

  • Fluidity is essential for membrane function (transport, signaling, and interactions with the environment). It must be balanced for structural integrity.

  • Factors influencing membrane fluidity:

    • Temperature: cold temperatures decrease fluidity (membrane becomes more rigid); warm temperatures increase fluidity (membrane becomes more fluid).

    • Phospholipid tail length: shorter tails increase fluidity; longer tails decrease fluidity due to more hydrophobic interactions and tighter packing. Short tails promote more movement; long tails restrict it.

    • Tail length range discussed: from about 14 to 24 carbons.

    • Saturation vs unsaturation of fatty acids: unsaturated tails (kinks due to double bonds) prevent tight packing and increase fluidity; saturated tails (straight chains) pack tightly and decrease fluidity.

    • Cholesterol: generally stabilizes the membrane; its effect depends on temperature and lipid composition, contributing to maintaining appropriate fluidity across temperatures.

  • Cells actively regulate membrane composition to maintain homeostasis and adapt to environmental changes.

  • The membrane is a dynamic interface with the environment; its fluidity and organization support nutrient uptake, signaling, and cell integrity.

Experimental evidence for membrane fluidity

  • A classic 1970 experiment demonstrated membrane protein movement in fused cells at different temperatures:

    • Setup: mouse cell membranes were fused and incubated at two temperatures: 0^{\circ}\text{C} (freezing) and 37^{\circ}\text{C} (body temperature).

    • At 0^{\circ}\text{C}: the membrane proteins remained largely immobile, staying on their original half of the membrane.

    • At 37^{\circ}\text{C}: the membrane proteins moved and redistributed across the shared membrane space.

  • This experiment supported the concept of membrane fluidity and the ability of proteins to diffuse within the membrane plane under physiological temperatures.

Structural constraints and membrane organization

  • In addition to the base fluidity, structural constraints are imposed in some membranes to organize function:

    • Proteins can be anchored to the cytoskeleton inside the cell to restrict movement or localization.

    • Proteins can be anchored to extracellular matrix components outside the cell.

  • These anchors help create functional zones in the membrane where specific activities occur, while the overall membrane remains fluid.

Practice prompt (summarized):

  • A common study exercise is to compare bacteria, plant cells, and animal cells across multiple features to understand similarities and differences.

  • Build a table listing features present or absent and explain how these features contribute to cell function.

Summary takeaways

  • Mitochondria and chloroplasts are semi-autonomous organelles with their own circular genomes and prokaryotic-like ribosomes, evidence for the endosymbiosis origin of these organelles.

  • They perform complementary energy-related roles in cells: chloroplasts capture light energy to build nutrients; mitochondria convert nutrients into ATP.

  • Protein sorting systems (co-translational and post-translational) ensure proteins reach their correct destinations.

  • ECM (in animals) and cell walls (in plants) provide structural support and protection through adhesive/structural proteins and glycosaminoglycans or cellulose, respectively.

  • The cell membrane is a dynamic, semi-fluid mosaic of phospholipids, proteins, cholesterol, and carbohydrates, with asymmetry between leaflets and various protein categories (transmembrane, lipid-anchored, peripheral).

  • Membrane fluidity is tightly regulated by temperature, lipid tail length, saturation, and cholesterol, and can be modulated by cellular architecture such as lipid rafts and protein anchors.

  • Experiments from the 1970s demonstrated real-time membrane dynamics, reinforcing the concept of a fluid mosaic model and the functional importance of membrane organization.