Cell Biology
What a cell is made of, how it runs, and how it divides
About this course
The cell from membrane to genome — transport and membrane potential, energy organelles, protein traffic and the cytoskeleton, then the cell cycle, signalling, cell death and cancer.
What you will be able to do
- Explain how membranes control transport and set up a potential across the membrane
- Describe how mitochondria and chloroplasts supply the cell's energy
- Trace a protein from synthesis to its destination through the secretory and recycling pathways
- Compare mitosis and meiosis and place each in the cell cycle
- Connect failures of signalling and cell-cycle control to cell death and cancer
What this course covers
- ATP turnover: recycling rate and daily production
- ATP value as a ratio, not a bond
- Proton motive force and the mitochondrial gradient
- ATP synthase: a rotary motor geared to the gradient
- Chloroplast photosystems and the cost of splitting water
- Endosymbiotic origin of mitochondria and chloroplasts
- Jagendorf–Uribe experiment: pH jump makes ATP
- Cytoskeleton as dynamic steady state
- Microtubule structure and dynamic instability
- Actin treadmilling and cell crawling
- Cytoskeletal drugs as rate modulators
- Myosin stroke and muscle speed via series/parallel arithmetic
- Intermediate filaments and composite cell mechanics
- Sliding filament experiment (1954) as a model of scientific reasoning
- DNA replication speed and parallelism
- Three-stage replication fidelity
- CDK–cyclin bistable switch and hysteresis
- Cell-size control: the adder rule
- Cell-cycle checkpoints and p53
- Cell cycle as a chain of engineering solutions
- Cooper–Helmstetter model of bacterial DNA content
- Cell Theory: Three Claims and Their Evidence
- Exponential Growth from Virchow's Third Claim
- Cell Size Set by Surface-to-Volume and Diffusion
- Prokaryotes vs. Eukaryotes: The Factor-of-400 Volume Difference
- The Diffraction Limit of Light Microscopy
- Epistemic Habits: Measuring, Checking, and Ranging Biology Numbers
- Pasteur's Swan-Neck Experiment as Decisive Evidence
- Signal arithmetic: molecules, receptors, and gain
- Noise floor of receptor counting
- Second messengers: cyclic AMP and calcium
- Cascade ultrasensitivity: dimmers become a switch
- Signal reach: diffusion, decay, and spatial range
- Adaptation and the off switch: responding to fold change
- Sutherland's fractionation: discovery of cyclic AMP
- Apoptosis: budget, mechanism, and switch
- Fractional killing from threshold variation
- Hayflick's counter derived from telomeres
- Three-lock architecture of the apoptotic switch
- Cancer as multi-step arithmetic with clonal expansion
- Peto's paradox and the six hallmarks
- Hayflick mixing experiment as experimental design
- Mitosis overview and three physics problems
- The spindle search: random growth, failure, and bias
- Failure as a design principle in the search
- The spindle checkpoint: chemical AND-gate for anaphase
- The pull: force capacity versus disassembly rate
- The cut, the count, and stacked error filters
- Reader et al. 1995: laser ablation experiment
- The DNA packing problem: length and scale
- Chromatin structure and the nucleosome
- The nuclear envelope, lamina, and nuclear pore complex
- Search time for a protein to find a nuclear pore
- Genome content and the C-value paradox
- The nucleolus as a membrane-less ribosome factory
- Hershey-Chase experiment: DNA as the genetic archive
- Cellular turnover: the steady-state numbers
- Lysosomal acid: proton counting and the pump's thermodynamic ceiling
- V-ATPase and ATP synthase as one reversible machine
- Protein turnover machinery: proteasome and autophagy
- The peroxisome and catalase kinetics
- Lysosomal recycling, storage diseases, and the lysosome as nutrient sensor
- De Duve's discovery of the lysosome by bookkeeping
- Hydrophobic effect and bilayer self-assembly
- Gorter and Grendel experiment and the 'right answer, wrong argument' lesson
- Counting bilayer molecules two independent ways
- Membrane permeability ladder and the price of admission
- Born-energy check on the ion barrier
- Membrane fluidity and FRAP measurement
- Fluid mosaic membrane as a workplace
- Protein production rate and signal addresses
- Reconstitution as experimental strategy
- Membrane map and budget of a liver cell
- Motor proteins versus diffusion
- Co-translational threading and quality control
- Pulse-chase timing of the secretory conveyor
- The secretory pathway as continuous directed flow
- Meiosis: one copy, two divisions
- Independent assortment and combinatorial diversity
- Crossing over: mechanism, counts, and spacing rules
- Sibling genome sharing and crossover count
- Meiosis I vs. mitosis: a distinct invention
- The egg's decades-long pause and cohesin decay
- Worked example: reading crossover count from sibling data
- Membrane potential is almost free to set
- Osmosis and osmotic pressure
- Channels, carriers, and the sodium-potassium pump
- The Nernst equation: a concentration gradient is a voltage
- The Goldman equation and the nerve impulse
- Synthesis: steady state, energy cost, and the lecture's central result
- Hodgkin–Horowicz experiment: testing and bounding Nernst
- Multicellularity: what was easy and what was hard
- Junctions, matrix mechanics, and bundle strength
- Diffusion limit and the hollow-sphere or fold solution
- Positional gradient reading and precision limits
- Toggle switch and epigenetic memory of cell identity
- Gregor et al. 2007: measuring gradient precision
- The spine: fourteen clauses and five course habits
Syllabus
The Cell and Its Membrane
- L1 · What a Cell Is, and How We Know
- L2 · The Membrane
- L3 · Transport, and the Potential Across the Membrane
Energy, Genome and Protein Traffic
- L4 · Energy, and the Two Organelles That Make It
- L5 · The Nucleus and the Genome
- L6 · Protein Traffic
Structure and Recycling
- L7 · The Cytoskeleton
- L8 · Lysosomes, Peroxisomes and Recycling
The Cell Cycle and Division
- L9 · The Cell Cycle
- L10 · Mitosis
- L11 · Meiosis
Signalling, Death and Multicellularity
- L12 · Cell Signalling
- L13 · Cell Death, and Cancer
- L14 · Multicellularity, and Where This Leads