BioSec 2012: Cheryl

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Trying to tie Computer Security into all of this

Using Darwin’s approach

  • Really slow: it took biology billions of years to get to the efficiency it now is at. How are we supposed to compete with that?
  • If we follow the same process we are setting up for failure most of the time…species getting extinct because they failed most of the time
  • Species survival is highly dependent on environment…computer security needs to basically work all the time independent of its environment …how is this going to work?

Programs = genotype (code/result) .exe = phenotype (produce) Exons= stuff that’s transcribed (5% or so) = spaghetti code Introns= junk stuff (95% or so) = comments




So for things to work:

  • there needs be a lot of redundant stuff:
    • Genes – redundant ways to get an amino acid
    • Genome – copies of the same genes
    • Pathways – many regulators
  • diversity
    • Biology is so good because there aren’t two things that are really the same…they have a lot in common…but there is that one small aspect that sets them apart…if they were all the same then one small thing just wipes all of them out
    • Can this be done with computers…randomize things by adding introns (junk code)?
  • Relationship to cell cycle
    • To enhance computer security, the cell (program) must learn to commit suicide (apoptosis). That is they need to learn how to recognize that they have been infected by a virus or something abnormal and then remove themselves from the entire network.



Textbook Notes

Chapter 1: Light and Life

  • Light
  1. source of information and energy
  2. Defined as EM radiation
  3. Wave of photons
  4. Can be absorbed by pigments and then used
  5. Colour = light that is not absorbed by pigment
  • Electrons become excited when absorbed by light which in turn then becomes potential energy (photosynthesis)
  • Photoreceptor
  1. light-sensing system
  2. made up of pigment molecule bound to protein
  3. eye = organ of animals to sense light
  • Problem:
  1. most light driven processes can only process a certain part of the EM spectrum
  2. source of energy…too much can cause deadly effects
  3. pigment melanin in our skin absorbs UV (high energy and can be damaging)
  • Circadian rhythms (body clock) the daily cycle of most living organisms have evolved to adapt to the change in light (night and day…plant use photosynthesis during the day and night break glucose)
  • Some animals prefer the dark (nocturnal animals like moths)
  • Some animals have ancestors that had functional eyes but are not blind (blind mole rat)
  • bioluminescent: organisms that use chemical energy to make their own light to attract a mate, camouflage, attract prey or communicate

Chapter 2: Origins of Life

  • life defined by seven characteristics:
  1. Display order: high ordered structures
  2. Harness and utilize energy: getting and using chemical energy to power the organism’s activities
  3. Reproduce: ability to reproduce their own kind
  4. Respond to stimuli: ability to respond environmental stimuli
  5. Exhibit homeostasis: ability to control an organism’s internal environment within the limits to sustain life
  6. Growth and development: consistent growth and development (DNA inheritance)
  7. Evolve: adapt to environments over many generations to have better reproducibility and survival of the species.
  • Cell theory
  1. All living organisms are composed of cells
  2. Cells are the functional units of life
  3. New cells come only from preexisting cells (division)
  • Eukaryotic Cells
Function Organelles/Structures involved
Genetic control of the cell Nucleus and ribosomes
Manufacture, distribution, and breakdown of molecules. Endoplasmic reticulum (ER), Golgi apparatus, lysosomes, vacuoles, and peroxisomes
Energy processing Mitochondria (plus chloroplasts in plant cells)
Structural support, movement, and communication between cells Structural support, movement, and communication between cells
  • Mitochondria and chloroplasts evolved by endosymbiosis which suggests mitochondria and chloroplasts were small prokaryotes and they began living within larger cells
  • Cytoskeleton:
    • network of protein fibers in the cells
    • functions in structural support and mobility
    • interacts with motor proteins resulting in mobility and cellular respiration
    • composed of three kinds of fibers:
  1. Microfilaments: (actin filaments) support the cell’s shape and are involved in mobility
  2. Intermediated filaments: (not present in plant cells) reinforces the cell shape and provides and anchor for the organelles
  3. Microtubules: (made from tubulin) responsible for cell rigidity and guiding the organelle’s movement

Chapter 3: Selection, Biodiversity and Biosphere

  • Biological organization:

Chapter3.png

  • Categorizing organisms on how they obtain carbon
  1. Autotrophs: create their energy-containing organic carbon molecules (glucose) from inorganic carbon molecules (sunlight). Example: plants using photosynthesis
  2. Heterotrophs: get energy-containing organic carbon molecules (glucose) by consuming other organisms. Example: animals eating plants or other animals.
  • Categorizing organisms on how they obtain energy
  1. Phototrophs: obtain energy from light
  2. Chemotrophs: obtains energy by oxidizing inorganic or organic substances
  • Theory of evolution: all organisms descended from one common ancestor, thus share common features. At the same time due to natural selection species change over time to adapt to their specific environment
  • All living organisms have three essential components:
  1. ATP for energy
  2. DNA for genetics
  3. Plasma membrane
  • Parasitism = symbiotic relationship where one organism benefits at the expense of the other
  • Mutualism = symbiotic relationship where both organism benefit
  • Interesting: The genetic barcode that is embedded in almost every cell is the mitochondrial cytochrome c oxidase 1

Computer security aspect

  • diversity
    • Biology is so good because there aren’t two things that are really the same…they have a lot in common…but there is that one small aspect that sets them apart…if they were all the same then one small thing just wipes all of them out
    • Can this be done with computers…randomize things by adding introns (junk code)?

Chapter 4: Energy and Enzymes

  • Cells can be basically thought of as a chemical factory (millions of chemical reaction take place in a cell)
    • Chemical reactions used for cell maintenance, manufacture of cell parts and cell replication
  • Energy is the capacity to do work
  • Two kinds of energy
  1. Kinetic Energy: energy of motion
  2. Potential Energy: energy that is stored as a result of its location or structure
  • Thermodynamics
    • the study of energy transformations that occur between a system (matter under study) and its surroundings (rest of the universe)
    • Two law of thermodynamics:
  1. Energy in the universe is constant
  2. Energy conversion increase entropy (measure of disorder/randomness)
  • Spontaneous reactions take place without having to input any energy from its surroundings and releases free energy that is influenced by two factors:
    • The changes in energy content
    • Entropy of the system
  • Chemical reactions either release or store energy
    • Exergonic reactions: release energy (ex: Cellular respiration - uses some of the released energy to produce ATP)
    • Endergonic reactions: stores energy or requires an input of energy; products have high potential energy (ex: photosynthesis – reactants = carbon dioxide and water (low energy), once absorbed energy from the sunlight produces products that are high in energy such as sugar)
  • Cells also couple energies, which uses the energy released from exergonic reactions to drive key endergonic reaction. This process usually uses the energy stored in ATP molecules.
  • ATP (Adenosine TriPhosphate) drives cellular work by energy coupling
    • Powers all cellular work
    • Is made up of: nitrogen base (adenine), sugar (ribose) and three phosphate groups
    • Phosphorylation is the hydrolysis of ATP which releases energy by transferring the third phosphate from ATP to some other molecule
    • ATP is a cycle – energy is released in an exergonic reaction (break down glucose) and is used in endergonic reaction (generation of ATP)
  • Biological molecules have a lot of potential energy, but it is not spontaneously released. Thus an energy barrier must be overcome before a chemical reaction can begin (Activation energy, EA )
  • Activation energy is the amount of energy that is needed for the reactants to move to a higher energy that is very unstable, thus forcing it to move to a lower energy that is stable.
  • There are many ways in which a reaction could be sped up:
    • Heat: makes sure the bonds between atoms break easier thus a allowing the reaction to proceed, but this could kill the entire cell
    • Enzymes: acts as a catalyst that lowers the activation energy needed for a reaction to begin thus speeding up the cell’s chemical reactions. This method increases the rate of a reaction without being consumed by the reaction.
      • Enzymes are very selective in the reaction it catalyzes and are specific determined by its shape (active site fits only specific substrate molecules)
      • Substrate: is the specific reactant that an enzyme acts on
      • Active site: a region of the enzyme that a substrate fits into
      • Every enzyme is most effective under optimal conditions such as temperature and pH. For example: at optimal temperature, the contact between the reactants and enzyme’s active site is at the peak.
      • Many enzymes also include cofactors, which are helpers that are inorganic ions (zinc, iron, copper) or organic nonprotien (called coenzymes such as vitamins). They bind to the active site and play a role in catalysis.
      • Regulation of enzyme activity is done by enzyme inhibitors, which is a chemical that interferes with an enzyme’s activity. There are two types of inhibitors:
  1. Competitive inhibitors: blocks substrates from entering the active site, which in turn reduces the enzyme’s productivity.
  2. Noncompetitive inhibitors: binds to the enzyme somewhere other than the active site which in turn changes the shape of the active site and thus preventing the substrate from binding to the enzyme.
  • Feedback inhibition occurs when the product acts as an inhibitor to one of the enzymes in the pathway that produced it.

Chapter 5: Membranes and Transport

  • Fluid mosaic model: a membrane structure that is composed of a bilayer of phospholipids with attached and embedded proteins.