Campbell Notes
Campbell Notes
Campbell Notes
Microscopy
Cell Fractionation
Types of cells
- Prokaryotic
o Bacteria
o Archaea
- Eukaryotic
o Fungi
o Animals
o Plants
o Protists: diverse group of mostly unicellular eukaryotes
- All cells:
o Bounded by selective barrier: plasma membrane (aka cell membrane)
o Semifluid, jellylike substance inside cells: cytosol, in which substances are
suspended
o Contain chromosomes, which carry genes in form of DNA
o Ribosomes, tiny complexes that make proteins according to instructions from
the genes
- Comparing:
o In e cells, most DNA is in nucleus, which is bounded by a double membrane. In p
cells, DNA is concentrated in region that is not membrane-enclosed, called the
nucleoid
o In e cells , the cytoplasm refers only to the region between the nucleus & plasma
membrane. Within the cytoplasm, suspended in cytosol, are a variety of
organelles of specialised form & function. Almost all p cells don’t have
membrane bounded structures but some contain regions surrounded by
proteins within which specific reactions take place
o E cells are generally larger. Size important for function (metabolism, produce
enzymes). A high
surface-to-volume ratio
facilitates the exchange of
materials
between a cell and its environment.
o Plasma membrane: selective barrier that allows passage of enough oxygen,
nutrients & wastes to service entire cell
Endomembrane System
- Regulates protein traffic & performs metabolic functions
- Many of the diff membrane-bounded organelle of the e cell are part of this system
- System includes:
o Nuclear envelope
o Endoplasmic reticulum
o Golgi apparatus
o Lysosomes
o Various kinds of vesicles & vacuoles
o Plasma membrane
- Carry out tasks in cell, incl. synthesis of protein, transport of proteins into membranes &
organelles or out of the cells, metabolism & movement of lipids & detoxification of
poisons
- Membranes in system are related either through direct physical continuity or by transfer
of membrane segments as tiny vesicles (sacs made of membrane)
Cytoskeleton
- Network of fibres that organises structures & activities in cell
- Extends throughout the cytoplasm
- Composed of three types of molecular structures: microtubules, microfilaments, and
intermediate filaments.
- Role:
o Give mechanical support to the cell & maintain its shape
o Stabilised by a balance between opposing forces exerted by its elements
o Provides anchorage for many organelles & even cytosolic enzyme molecules
o Can be quickly dismantled in 1 part of cell & reassembled in new location,
changing the shape of cell
Tight junctions
- Barrier that prevents leakage of extracellular fluid across a layer of epithelial cells
Desmosomes
- Fasten cells together into strong sheets
Gap functions
- Provide cytoplasmic channels from 1 cell to an adjacent cells
- Consists of membrane proteins that surround a pore through which ions, sugars, amino
acids & other small molecules may pass
- For communication between cells in many types of tissues
Subatomic Particles
- Tiny bits of matter are composed of subatomic particles
- Protons: +ve charge
- Electrons: -ve charge
- Neutron: neutral charge
- Protons and neutrons are packed tightly in dense
core: atomic nucleus at center of atom (P gives
nucleus +ve charge)
o Rapidly moving electrons form a “cloud” of -
ve charge around the nucleus
o The attraction between op. charges keeps
the electrons in the vicinity of the nucleus
- Dalton: used to measure atoms & subatomic
particles (same unit as atomic mass unit)
- Protons & Neutrons have same mass: close to 1
Dalton
- Electrons has mass of about 1/2000 that of a N or P
Atomic Number & Atomic Mass
- Atomic number: number of protons unique to element
- Mass number: total number of protons and neutrons in nucleus
Isotopes
- Are diff atomic forms od the same element
- Radioactive isotope: nucleus decays spontaneously, giving off particles & energy
o When it leads to change in no. of protons, it transforms the atom to an atom of a
diff element
o E.g. when an atom of carbon-14 (14C) decays, it loses a proton, becoming an
atom of nitrogen (14N)
Radioactive Tracers
- Radioactive isotopes often used as diagnostic tools in medicine
o Are incorporated into biologically active molecules which are then used as
tracers to track atoms during metabolism
- Certain kidney disorders are diagnosed by injecting small doses of radioactively labelled
substances into the blood, then analysing the tracer molecules excreted in the urine.
- Also used in combination with sophisticated imaging instruments, such as PET scanners
that can monitor growth and metabolism of cancers in the body
- Radiation from decaying isotopes is hazard to life by damaging cellular molecules
o Severity of this damage depends on the type & amount of radiation an organism
absorbs
o Doses used in medical diagnosis are safe
Radiometric Dating
- In fossils, radioactive decay is measured to date relics to past life
o Provide large body of evidence for evolution
o Diff between organisms from the past & present to give insight into species that
disappeared over time
- “Parent” isotope decays into its “daughter” isotope at fixed rate
o Half-life: time taken for 50% of the parent isotope to decay
- Each radioactive isotope has characteristic half-life not affected by temp, pressure or
any other enviro variable
- Radioactive dating: measures ratio of diff isotopes & calculate how many half-lives (in
yrs) have passed since organism was fossilised
o Range from seconds to billion years
- Electrons are found in diff electron shells, each with a characteristic avg distance &
energy level
o Can move from shell to shell by absorbing/losing amount of energy = to diff in PE
between position in old & new shell
o Absorbs: farther out of nucleus
o Loses: falls back to shell closer to nucleus. Lose energy released to enviro as heat
- Closer the electrons is to the nucleus, the lower PE
Electron Orbitals
- Orbital: 3D space where electron is found 90% of the time
o Exact location of location never known
o Used to describe the space
Covalent Bonds
- Covalent bonds: sharing of a pair of valence electrons by 2 atoms
- Molecules: 2 or more atoms held together by covalent bonds
- Ways to represent electron sharing:
o Molecular form: H2
o Lewis dot structure: H:H
o Structural formula: H – H
Line represents single bond: pair of shared electrons
o Space filling model:
Ionic Bonds
- Ions: When the more EN atom takes an electron away from its partner. Result from op
charged atoms/molecules
- Cation: +ve charged ion
- Anion: -ve charged ion
- Because they are op. charged, they attract each other known as an ionic bond
Hydrogen Bonds
- The attraction between a H (δ+) and an electronegative atom
- In living cells: partners usually O & N atoms
- When atom forms covalent bonds, the orbitals in valence shell undergo rearrangement
- Molecular shape crucial:
o Determined how biological molecules recognise & respond to 1 another with
specificity
o Biological molecules only bind if shape are complementary
- E.g. opiates (drugs) relieve pain & alter mood by weakly binding to specific receptor
molecules on surfaces of the brain cells.
o Why would brain cells carry receptors for opiates, compounds not made by
body?
o Because they have similar shape to endorphin & mimic them by binding to
endorphin receptors in brain
Chemical reactions
- Chemical reactions: the making & breaking of chem bonds that lead to changes in
composition of matter
- Reactants: starting materials
- Products: resulting materials
- Reaction between H & O forming water:
- Summarise photosynthesis:
- Reverse reaction: H & N molecules can combine to form NH3 & can decompose to
regenerate H & N:
Hydrogen Bonds
- Shape: wide V with 2 H atoms joined to O atom by single covalent bonds
o O is more electro-ve than H so electrons closer to O than H: polar covalent
bonds
Evaporative Cooling
- Molecules of any liquid stay close together through attraction. Molecules moving fast
enough overcome attractions to depart liquid & enter air as gas (vapor)
- Vaporisation/evaporation: transformation from liquid to gas
- Even a low temps, the speediest molecules can escape into air (occurs at any temp)
o E.g. glass of water at room temp will eventually evaporate completely
- If a liquid is heated, the avg KE of molecules >es & the liquid evaporates more rapidly
- Heat of vaporization: quantity of heat a liquid must absorb for 1g of it to be converted
from the liquid to the gaseous state
o To evaporate 1 g of water at 25°C, about 580 cal of heat is needed—nearly 2x
amount needed to vaporize a gram of alcohol or ammonia.
o For the same reason that water has a high SH, it also has a high heat of
vaporization relative to most other liquids
o Resulting from the strength of its H bonds, which must be broken before the
molecules can exit from the liquid in the form of water vapor
- Effects of high amount of energy required to vaporize water:
o Global scale: helps moderate Earth’s climate. Considerable amount of solar heat
absorbed by tropical seas is consumed during the evaporation of surface water.
As moist tropical air circulates poleward, it releases heat as it condenses &
forms rain
o Organismal level: accounts for the severity of steam burns, caused by the heat
energy released when steam condenses into liquid on the skin.
- As liquid evaporates, the surface of the liquid that remains behind cools down (its temp
<es)
o This evaporative cooling occurs because the “hottest” molecules, those with the
greatest KE, are most likely to leave as gas
o E.g. 100 fastest runners at a college transferred to another school, the avg speed
of the remaining students would decline
- Effects of evaporative cooling:
o Stability of temp in lakes & ponds
o Prevents terrestrial organisms from overheating
o Evaporation of water from the leaves of a plant helps keep the tissues in the
leaves from becoming too warm in sunlight
o Evaporation of sweat from human skin dissipates body heat & helps prevent
overheating on a hot day/when excess heat is generated by activity
o High humidity on a hot day >es discomfort - high concentration of water vapor in
the air prevents evaporation of sweat from the body
- By convention, H+ (does not exist on its own in aq solution) is used to represent H3O+
- Double arrows = reversible reaction that reaches a state equilibrium when water
molecules dissociate at same rate that they are being reformed from H+ & OH-
o At equilibrium point, concentration of water molecules greatly exceeds concen.
of H+ & OH-
o In pure water 1 in every 554m is dissociated (rare)
o concentration of H+ and of OH- in pure water is therefore 10-7 M (at 25°C)
o Important: H+ & OH- are very reactive – changes in their concen. affect cell’s
proteins & other complex molecules
- In pure water:
o Concentration of H+ & OH- are equal
o Adding certain kinds of solutes, called acids & bases disrupts balance
- pH scale: describe how acidic or basis a solution is
Indirect: dissociating to form hydroxide ions which combine with H ions &
form water
- Basic solutions: solutions w/ higher concentration of OH- than H+
- Neutral: H+ & OH- concentrations are equal
- Weak acids: acids that reversibly release & accept back H ions
The pH Scale
- In aq solution at 25°C, the product of H+ & OH- concentrations is constant at 10-14
Buffers
- Slight change in pH harmful because chem processes of cell are sensitive to
concentrations of H & OH ions
- Example: blood – pH very close to 7.4, slightly basic
o Person cannot survive for more than few min if pH drops to 7 or rises to 7.8
o Chem system in blood maintains stable pH (buffers)
- 0.01 mol of strong acid added to 1L pure water
o pH drops from 7 to 2, BUT
o Same amount added to blood: pH from 7.4 to 7.3
- Buffers: substances that allow biological fluids to maintain relatively constant pH
despite addition of acids or bases
o Minimises changes in concentrations of H+ & OH- in solution
o Accepts H ions when solution are in excess & donates H ions if they have been
depleted
o Most contain weak acid & its corresponding base (combine reversibly with H
ions)
- Carbonic acid:
o Contributes to pH stability in blood & many other biological solutions
Carbon atoms
- C can form four bonds: great diversity
- Chem characteristic of an atom linked to electron configuration
o Determines kinds & no. of bonds an atom will form with other atoms
Hydrocarbons
- Organic molecules consisting of only C & H
- Atoms of H are attached to C skeleton whenever electrons are available for covalent
bonding
- HC are major components of petroleum, called fossil fuel because it is composed of
decomposed remains of organisms that lived m of yrs ago
- Although HC are not prevalent in most living organism, many cell’s organic molecules
have regions consisting of only C & H
- E.g. molecules known as fats have long HC tails attached to a non-HC component
- Neither petroleum nor fat dissolve in water: both are hydrophobic compounds because
bonds are non-polar C-to-H linkages
- HC undergo reactions that release large amount of energy
Isomers
- Compounds that have same molecular formula but diff structures
- Structural isomers: diff in covalent arrangements of their atoms
Chemical Groups
- Functional groups: chem groups that affect molecular shape, contributing to function
- E.g. Estradiol (type of estrogen) & Testosterone
o Both are female & male sex hormones
o Are steroids, organic molecules with common carbon skeleton in form of 4 fused
rings
o Differ only in chem groups attached to rings (in blue in figure), contributing to
function:
- 7 chem groups most important in biological processes:
o 1st 6 groups can be chemically reactive
o Of the 6, all except sulfhydryl are hydrophilic (soluble)
o Methyl group not reactive, but serves as recognisable tag on biological molecules
ATP: Source of Energy for Cellular Processes
- ATP (adenosine triphosphate): more complicated organic phosphate
- Consists of an organic molecule called adenosine attached to a string of 3 phosphate
groups:
- When 3 phosphates are present, as in ATP, 1 phosphate may be spilt off as result of
reaction with water
- Having lost 1 phosphate, ATP becomes adenosine diphosphate, or ADP
- ATP: sometimes said to store energy, but more accurate to think of it as storing the
potential to react with water
- Reaction releases energy that can be used by the cell.
Carbon: Summary
- Versatility of C – great diversity (can form 4 bonds)
- Properties emerge from unique arrangement of its skeleton & chem groups attached
The Structure and Function of Large Biological Molecules
Macromolecules
- Are polymers built from monomers
- Polymer is a long molecule consisting of many similar/identical building blocks linked by
covalent bonds
o E.g. large carbohydrates, proteins & nucleic acids
- Monomers: repeating units that serve as building blocks of polymers
o Form polymers
o Some have their own function
- Each class of polymer is made up of a diff type of monomer
o But chem mechanisms by which cells make & break down polymers are same
Carbohydrates
- Serve as fuel & building materials
- Include sugars & polymers of sugars
- Simplest carbohy. are monosaccharides (simple sugars), and are monomers from which
more complex carbohydrates are built
- Disaccharides: double sugars consisting of 2 monosac. joined by a covalent bond
- Carbohy. macromolecules are polymers called polysaccharides, composed of many
sugar building blocks
Sugars
- Monosaccharides: have molecular formulas that are some multiple of the unit CH2O
o E.g. Glucose (C6H12O6)
- Trademarks of a sugar:
o 1 carbonyl group (C=O) & multiple hydroxyl groups (OH)
- Depending on location of carbonyl group, a sugar is either a:
o Aldose (aldehyde sugar): at end of C skeleton
o Ketose (ketone sugar): within C skeleton
o Glucose is an aldose but fructose (an isomer of glucose) is a ketose
- Criterion for classifying sugars:
o Most names end in -ose
o Size of the carbon skeleton ranges from 3 to 7 carbons long
Hexoses: have 6 carbons e.g. glucose & fructose
Trioses: 3 C sugars
Pentoses: 5 C sugars
Polysaccharides
- Macromolecules, polymers with a few 00 to 000 monosac. joined by glycosidic linkages
- Function:
o Storage material, hydrolysed to provide sugar for cells
o Building material for structures that protect the cell/whole organism
- Architecture & function are determined by its sugar monomers & by position of its
glycosidic linkages
Storage Polysaccharides
- The form that plants & animals store sugars for later use
- Plants store starch, a polymer of glucose monomers, as granules within cellular
structures known as plastids (which incl. chloroplasts)
o Synthesising starch enables plant to stockpile surplus glucose
o Glucose = major cellular fuel, starch = stored energy
o Sugar can later by withdrawn from its carbohy. ‘bank’ by hydrolysis breaking
bond between glucose monomers
- Most animals have enzymes that can hydrolyse plant starch, making glucose for nutrient
for cells
o Major sources of starch in diet: potato tubers & grains, fruits of wheat, corn, rice
o Most glucose in starch are joined by 1-4 linkages (no. 1 C to no. 4 C), like maltose
o Simplest form of starch, amylose, is unbranched
o Amylopectin, more complex starch, is branched polymer with 1-6 linkages at
branch points
- Animals store a polysac. called glycogen, a polymer of glucose that is more extensively
branched
o Vertebrates store mainly in liver & muscle cells
o Hydrolysis of glycogen in these cells releases glucose when demand for sugar
increases
o Stored fuel cannot sustain animal for long
o In humans, glycogen stores are depleted in about a day unless they are
replenished by eating
o Low carbohy. diets result in weakness & fatigue
Structural Polysaccharides
- Build strong materials
- Cellulose (polysac.) is major component in tough walls that enclose plant cells
o Plants produce 100b tons of cellulose per year
o Most abundant organic compound on Earth
o Like starch, has 1-4 glycosidic linkages, BUT linkages in these 2 polymers differ: 2
slightly diff ring structures for glucose
- When glucose forms a ring, the hydroxyl group attached to the no. 1 C is positioned
either below or above plane of ring
o 2 ring forms for glucose are called alpha (α) and beta (β)
o In starch, all glucose monomers are in α configuration
o In cellulose, glucose monomers are in β configuration, making every glucose
‘upside down’ with respect to its neighbours
Lipids
- A diverse group of hydrophobic molecules
- Are 1 class of large biological molecules that does not incl. true polymers
- Generally not big enough to be considered macromolecules
- Lipids are grouped with e/o because they share 1 important trait: mix poorly with water
- Hydrophobic behaviours are based on molecular structure
- Have some polar bonds associated with O, lipids consist mostly of HC regions
- Varied in form & function
- Incl. waxes & certain pigments
Fats
- Not polymers, BUT are large molecules assembled from smaller molecules by
dehydration reactions
- A fat is constructed from 2 kinds of smaller molecules: glycerol & fatty acids
Phospholipids
- Major constituents of cell membranes
- Is similar to a fat molecule BUT has only 2 fatty acids attached to a glycerol rather than 3
o The 3rd hydroxyl group of glycerol is joined to a phosphate group, which has a -ve
electrical charge in the cell
o Typically, an additional small charged/polar molecule is linked to the phosphate
group
- 2 ends of phospholipids show diff behaviours with respect to water
o The HC tails are hydrophobic & are excluded from water
o The phosphate group & its attachments form a hydrophilic head
- When phosphates are added to water, they self-assemble into a double-layered sheet
called a “bilayer” that shields their hydrophobic fatty acids tails from water
- At surface of a cell:
o Hydrophilic heads of the molecules are on outside of bilayer, in contact with
aqueous solutions inside & outside of the cell
o Hydrophilic tails point towards interior of bilayer, away from water
- Phospholipid bilayer forms boundary between cell & its external enviro & establishes
separate compartments within eukaryotic cells
Steroids
- Are lipids, characterised by a C skeleton consisting of 4 fused rings
- Chem groups attached to the rings distinguish them from others
- Cholesterol: a type of steroid and is a crucial molecule in animals
o Common component of animal cell membranes
o A precursor from with other steroids, such as sex hormones, are synthesised
- In vertebrates, cholesterol is synthesised in the liver & is obtained from the diet
- High level of cholesterol in blood may contribute to atherosclerosis (CVD)
Cellular membrane
- Are fluid mosaics of lipids & proteins which are stable ingredients of the membrane
(carbohy. also important)
- Ability of phospholipids to form membranes is inherent in their molecular structure:
o Amphipathic molecule: has both hydrophilic & hydrophobic region
- A phospholipid bilayer can exist as a stable boundary between 2 aq compartments
because hydrophobic tails are sheltered from water while hydrophilic heads are
exposed to water
- Most membrane proteins are amphipathic
o Reside in phospholipid bilayer with their hydrophilic regions protruding
o Maximises contact of hydrophilic regions of proteins with water in the cytosol &
extracellular fluid
o Provides hydrophobic parts with a non-aq enviro
- Fluid Mosaic Model: membrane is a mosaic of protein molecules bobbing in a fluid
bilayer of phospholipids
o Currently accepted model of arrangement of molecules in plasma membrane
o Proteins are not randomly distributed in membrane
o Groups of proteins often associated in long-lasting, specialised patches, where
they carry common functions. Called lipid rafts because specific lipids are found
in patches
- Membrane remains fluid as temp <es until the phospholipids settle into a closely packed
arrangement & membrane solidifies (bacon grease turning into lard when cool)
- Temp at which membrane solidifies depends on types of lipids it is made of
o As temp <es, the membrane remains fluid to a lower temp if it is rich in
phospholipids with unsaturated HC tails
o Because of kinks in the tails where double bonds are located, unsaturated HC
tails cannot pack together as closely as saturated HC tails, making membrane
more fluid
- The steroid cholesterol, wedged between phospholipid molecules in plasma membranes
of animals cells, has diff effects on membrane fluidity at diff temps
o At high temps: e.g. 37 C, cholesterol makes the membrane less fluid by
restraining phospholipid movement
o Because it also hinders the close packing of phospholipids, it lowers the temp
required for the membrane to solidify.
o Thus, cholesterol can be thought of as a “fluidity buffer” for the membrane,
resisting changes in membrane fluidity that can be caused by changes in temp
o Compared to animals, plants have very low levels of cholesterol; steroid lipids
buffer membrane fluidity in plant cells.
-
- Fluidity of a membrane affects both its permeability & the ability of membrane proteins
to move to where their function is needed
o When membrane solidifies, its permeability changes, & enzymatic proteins may
become inactive if their activity requires movement within the membrane
o Membranes that are too fluid cannot support protein function
- Extreme enviro are a challenge for life, resulting in evolutionary adaptations that include
diff in membrane lipid composition
- E.g. CD4 is a protein on the surface of immune cells: helps HIV infect these cells, leading
to AIDS
o Some don’t have AIDS & show no evidence of HIV infected cells
o Resistant people have an unusual form of a gene that codes for an immune cell-
surface protein called CCR5
o Although CD4 is the main HIV receptor, HIV must also bind to CCR5 as a “co-
receptor” to infect most cells
o An absence of CCR5 on the cells of resistant individuals, due to the gene
alteration, prevents the virus from entering the cells
o Interfering with CD4 causes dangerous side effects because of its many
important functions in cells
o Discovery of the CCR5 co-receptor provided a safer target for development of
drugs that mask the protein & block HIV entry
The Role of Membrane Carbohydrates in Cell-Cell Recognition
- Cell-cell recognition: cell’s ability to distinguish 1 type of neighbouring cell from another
(crucial to functioning of organism)
- Important for e.g.:
o Sorting of cell into tissues & organs in animal embryo
o Rejection of foreign cells by immune system
- Cell recognise other cells by binding to molecules, often containing carbohy., on the
extracellular surface of the membrane
- Membrane carbohy.:
o Usually short, branched chains of fewer than 15 sugar unites
o Some are covalently bonded to lipids, forming molecules called glycolipids
o Most are covalently bonded to proteins, called glycoproteins
- The carbohy. on the extracellular side vary from species to species, among individuals of
the same species, and even from one cell type to another in a single individual
- Diversity of the molecules & their location on the cell’s surface enable membrane
carbohy. to function as markers that distinguish 1 cell from another
o The four human blood types designated A, B, AB, and O reflect variation in the
carbohydrate part of glycoproteins on the surface of RBC