Biol 1090 Flashcards

1
Q

Enucleation

A

The process where cells (red blood cells) eject their nucleus.

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2
Q

Differentiation

A

Cells specialize

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3
Q

Miller Urey Experiment and key takeaways

A

Simulated conditions on early earth and found that that simple inorganic compounds in the presence of energy can form simple then later more complex organic compounds. Some of which are amino acids.

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4
Q

Primordial Hypothesis
(Oparin’s and Haldane’s)

A

Commonly accepted conditions on primative earth favored chem rxns that synthesis more complex organic compounds from simpler inorganic precursors.

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5
Q

Cell Theory

A
  1. All living organisms are composed of 1 or more cells
  2. Cell is the most basic unit of life (first 2 by Schleidon and Shwann)
  3. All cells come from cells (Virchow)
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6
Q

Basic Properties of Cells

A
  1. Highly complex and organized
  2. Activity controlled by genetic programing
  3. Can reproduce
  4. Assimilate and Use energy
  5. Carry out chem rxns (enzymes)
  6. Engage in mechanical activities (engulf)
  7. Respond to Stimuli
  8. Capable of self regulation
  9. Evolve
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7
Q

Prokaryotes

A

Bacteria and Archaea
- no defines nucleus or organelles
- single celled orgs
- 1-10 nanometers
- small ribosomes
- reproduce asexually
- genetic material in nucleoid
- DNA is circular fashion (plasmid)

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8
Q

Eukaryotes

A

Fungi, plants, animals, protozoa
- multicellular organisms
- 10-100 nanometers
- nucleus and organelles
- ribosomes are large
- genetic material in nuclear compartment (chsomes)

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9
Q

Eukaryotes - Animals

A
  • lysosomes
  • microvilli
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10
Q

Eukaryotes - Plants

A
  • cell walls
  • vacuoles (turgor pressure)
  • chloroplasts
  • plasmodesmata (connect neighboring plant cells)
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11
Q

Virus Genome

A

DNA or RNA

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12
Q

Virus

A

macromolecular packages that can function and reproduce only with living cells.

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13
Q

Virion

A

Inanimate particle outside cells

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14
Q

Virus Baltimore Classification

A

Retrovirus - RNA type, can insert a copy of its genome into a DNA host cell
Hepadnavirus - DNA type
Filovirus - single stranded negative sense DNA
Adenovirus - resperatory illness
Bacteriophage - Infects and replicates within bacteria and archaea

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15
Q

Negative Sense RNA

A

must be transcribed to mRNA

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16
Q

Positive Sense RNA

A

can be directly translated into proteins

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17
Q

Host Range

A

Narrow - infect cells in just a specific part of humans
Wide - (rabies) can infect humans, bats, foxes, racoons

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18
Q

Non-lytic

A

Viral DNA or RNA inserts into host genome (provirus). Infected cell can survive often with impaired function

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19
Q

Lytic

A

Production of virus particles ruptures and kills the cell

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20
Q

Monopartite

A

Entire genome occupies one nucleic acid molecule

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21
Q

Multipartite

A

Genome occupies several nucleic acid segments

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22
Q

RNA Vaccines

A

Tricking body cells into producing fragments of a virus (antigens).
Can be made more effective by incorporating instructions for a replicase (to make more antigens)

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23
Q

HIV

A

Retrovirus - inserts copy of genome into DNA host cell (stays in DNA forever_

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24
Q

Hepadnavirus

A

Hepatitis B

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25
Q

Filovirus

A

Ebola

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26
Q

Adenovirus

A

Cold and Flu

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27
Q

Bacteriophage

A

Attack bacteria and archaea

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28
Q

Slime molds

A
  • eukaryotic single celled organisms
  • reproduce with spores
  • many nuclei
  • can move around and respond to environment
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29
Q

Virus (Yes) can/are

A
  • complex and organized
  • controlled by genetic programing
  • reproduce (yes and no)
  • evolve
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30
Q

Only in plant cells

A
  • chloroplasts
  • cell wall
  • vacuoles
  • plasmodesmata
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31
Q

Only in animal cells

A
  • lysosomes
  • microvilli
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32
Q

Phospholipid bilayer properties

A
  • trilaminar (lipid bilayer)
  • made of lipids (phospholipids)
  • hydrophobic and hydrophilic parts (phospholipids are amphipathic)
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33
Q

Phospholipids Structures/patterns

A

Micelle - circular no lumen
Liposome - circular two layers lumen
Bilayer sheet - (trilaminar)

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34
Q

Phospholipids (structure)

A
  • 2 fatty acyl molecules (esterified 1,2)
  • glycerol
  • phosphate (3 by phosphate residue)
  • variable portion of head group (choline, serine, inositol)
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35
Q

Sphingolipid

A
  • glycerol replaced with sphingosine
  • amide linked to fatty acid and phosphate group
    enriched in nervous system (signal transduction + cell recognition)
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36
Q

Fluid mosaic includes

A
  • phospholipids
  • peripheral, transmembrane proteins
  • ## cholesterol
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37
Q

Lipid Rafts

A

Portions of the bilayer that include a higher concentration of specific proteins like sphingolipids or cholesterol

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38
Q

Types of membrane proteins

A
  • integral
  • peripheral
  • lipid anchored
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39
Q

Integral proteins and functions

A
  • transport of nutrients and ions
  • cell-cell communication
  • attachment
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40
Q

How can temperature affect lipid structure

A
  • denaturation of lipids
  • exchange of lipid chains
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41
Q

Transmembrane protein structure

A
  • ## hydrophobic portion within bilayer (alpha helices) (transmembrane protein domain)
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42
Q

TM4SFs Tetraspanins

A
  • 4 alpha helices
  • 2 extracellular domains
    cell, adhesion, motility, proliferation
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43
Q

Simple Diffusion

A
  • passive
  • non-mediated
  • will concentration gradient (down)
  • small uncharged particles (CO2, O2)
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44
Q

Diffusion through Channel

A
  • passive
  • non-mediated
  • through channels
  • small charged particles
    Na+, K+, Ca2+, Cl-
  • down concentration gradient
  • channels are selective
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45
Q

Facilitated Diffusion

A
  • passive
  • mediated
  • substrate binds directly to facilitative transporter
  • change in conformation allows compound to be released on other side
  • down concentration gradient
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46
Q

Active Transport

A
  • active
  • mediated
  • substrate binds to active transporter
  • hydrolysis of an ATP molecule allows molecules to be released on other side
  • against gradient
    Na+/K+ transporter (maintains action potential)
  • 3Na+ out, 2K+ in for each ATP
  • against gradient
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47
Q

Ion Channels

A

Allows channels to respond to stimuli
1) voltage-gated (Na+, K+)
- respond to changes in charge (action potential)
2) Ligand-gated (acetylcholine)
- responds to binding of a specific molecule on surface of ligand
- causes a conformational change to channel

48
Q

Ways of targeting ion channels

A

TTX - Na+ channel blocker
- binds to voltage-gated Na+ channels and blocks passage of Na+ (inhibits firing of action potentials)
Curare - competitive antagonist
- occupies same position on receptor and causes no response

49
Q

Symporter

A
  • rely on chem gradient of another molecule to push a compound up its concentration gradient
  • Na+ glucose symporter (2Na+ 1 glucose) (Na+ is with gradient into cell)
50
Q

Antiporter

A
  • concentration gradient of one molecule is used to transfer a second molecule in opposite direction
  • Na+/H+ exchanger
  • Na+ into cell, H+ out of cell
51
Q

Cell Structure (hypertonic, hypotonic, isotonic)

A

Hypertonic - more solute out of cell, shrink
Isotonic - normal
Hypotonic - more solute in cell, burst/lysed

52
Q

Signal Transduction

A
  • binding of ligand to a receptor
  • signal transduction via second messenger (cAMP, calcium, G-protein)
  • cellular response
53
Q

Glycogenolysis

A

epinephrin converting glycogen in liver to glucose
- glycogenin(acts as a primer to polymerize first glucose molecule) surrounded by glucose units

54
Q

Anchor Proteins

A
  • interact with components of the ECM
55
Q

ECM (extracellular matrix) roles

A

Abundant in connective tissues
- cell adherence
- communication between cells - - cell shape, mechanical support, structural integrity
- serves as barrier, filters out some particles

56
Q

ECM components

A
  • proteins (collagen)
  • glycoproteins (laminin, fibronectin)
  • proteoglycans (proteins with chains of polysaccharides)
57
Q

Plant Cell Walls (ECM)

A
  • cellulose, hemicellulose, pectin, proteins
  • structural support
  • protection
58
Q

Theory of Endosymbiosis and Evidence

A
  • organelles from euk cells with two membranes (mit, chlo) are formerly free living prokaryotes taken inside one another in endosymbiosis
    Evidence:
    1) binary fission of mitochondria and plastids
    2) circular DNA in organelles like bacteria
59
Q

Aerobic cellular respiration

A

Converting glucose to energy (stored in ATP) in the presence of oxygen

60
Q

Outer Mitochondrial Membrane

A
  • contains many enzymes (monoamine oxidases)
  • has porins (for ATP, sucrose)
61
Q

Inner Mitochondrial Membrane

A
  • high protein to lipid ratio (3:1)
  • double layers fold called cristae
  • rich in cardiolipin - phospholipid (optimal membrane function)
62
Q

Mitochondrial Matrix Makeup

A

Matrix - high protein content, gel like consistency, contains mitochondrial ribosomes and DNA

63
Q

Substrate level phosphorylation

A

*specific to glycolysis
- hydrolysis rxns release enough energy to phosphorylate ADP to ATP
12% or ATP

64
Q

Oxidative phosphorylation

A
  • chemical energy of organic molecules is transferred first to electron carriers to create an electrochemical gradient to power ATP synthesis
    88% of ATP
65
Q

Electron Carriers

A

Oxidized - accepts e
Reduced - donates e
NAD+, NADH
FAD, FADH2

66
Q

Photosynthesis

A

building carbs using energy from sunlight and CO2

67
Q

Light-Dependent Reactions

A
  • occurs in thylakoid membranes
  • chlorophyll is light harvesting complex
    -e enters ETC
    H+ pumped into thylakoid lumen
68
Q

Light-Independent Reactions

A

Calvin Cycle
- occurs in stroma
- ATP and NADPH made in light reaction used to make CH2O

69
Q

Apoptosis

A

Death of a cell in a coordinated sequence of events

70
Q

Roles of Apoptosis

A

bmp - expression of non-active MnpReceptors in duck embryonic limbs results in webbed feet (reduces apoptosis)
Plants - uses apoptosis to cause fenestrated leaves

71
Q

Apoptotic Cells (characteristics)

A
  • shrinkage
  • blebbing (bulging of plasma membrane)
  • fragmentation of DNA or nucleus
  • engulfment by phagocytosis
72
Q

Cytochrome C

A

causes production of caspases
- disrupts cell adhesion
- destroy lamins
- breaks down cytoskeleton
- activates DNase

73
Q

Apoptosis and Diseases

A

too little - cancer
too much - alzheimers, parkinsons

74
Q

Cytoplasmic Endomembrane system

A
  • ER
  • endosomal transport vesicles
  • golgi complex
  • lysosomes
  • vacuoles
75
Q

Secreted Proteins (mucin)

A
  • synthesized in rough ER
  • processed in the ER
  • processed in golgi
  • concentrated in vesicles
  • delivered to plasma membrane for secretion
76
Q

GFP Tracking

A

Green Fluorescent Protein from Jellyfish
- can be fused with other cellular proteins
- can be expressed in cells when fused

77
Q

Vesicular Transport

A

uses transport vesicles
- movement - uses cytoskeleton and motor proteins (anterograde or retrograde)
- tethering - via RAB proteins
- docking - uses SNARE proteins (provides energy for fusion)
- fusion - fuses vesicle and target membrane

78
Q

Exocytosis + Endocytosis

A

Exocytosis - e.g organelle to plasma membrane
e.g secretion of neurotransmitters
Endocytosis - e.g PM to organelle
e.g Activity-dependent internalization pf AMPA receptors

79
Q

Rough ER

A
  • have ribosomes
  • protein processing
  • synthesis of membrane phospholipids
  • glycosylation of proteins
  • protein folding and quality control (chaperone)
  • Protein synthesis, modification, and transport
80
Q

Smooth ER

A

-no ribosomes
- lipid synthesis
- production of steroid hormones
- detoxification
- sequestration (storage of Ca2+)
Ca2+ in cytosol is:
- bound by Ca2+ binding proteins
- forced through pumps and transporters
- or sequestered (in sinks)

81
Q

Where are proteins translated (free vs. bound)

A
  • free - cytosolic prots, peripheral membrane prots, prots to nucleus, mitochondria, peroxisomes, or chloroplasts
  • bound - secreted prots, integral membrane prots, soluble prots associated with lumen of endomembrane system
  • all protein translation begins on free ribosomes not associated with the ER
82
Q

Signal Sequence

A

to target ribosomes to ER membrane
- amino terminus
- contains consecutive hydrophobic amino acids
- directs synthesis to ER compartment

83
Q

Endocytic Pathways of Protein Sorting

A

1) protein retained in ER
2) transported to golgi (futher modifications), and delivered to distal parts of secretory pathway (maybe outside the cell)

84
Q

Zellweger Syndrome

A
  • no peroxisomes made (mutation)
  • autosomal recessive
  • brain development defects
  • hypomyelination
  • apnea
  • abnormal renal function
  • does not survive a year
85
Q

Cystic Fibrosis

A
  • mutation in CFTR
  • deletion of 3 nucleotides
  • loss in phenylalanine (508)
  • proteins degraded in ER fail to reach surface
    OR
  • CFTR transporter affected
  • cannot produce proper lubricating fluid in lungs
  • sticky lung
86
Q

ER to Golgi pathway

A

Proximal to distal
Cis to Medial to Trans

87
Q

Golgi Complex Structure

A
  • smoot flattened cisternae
  • about 8 cisternae per stack
  • few to thousand of stacks per cell
  • curved
  • polarity
  • cisternae biochemically unique (different enzymes to modify)
  • membrane supported by protein skeleton (actin, spectrin)
  • scaffold linked to motor proteins that direct movement of vesicles into and out of golgi
88
Q

CGN and TGN

A

CGN - sorting station (should proteins continue on to next golgi or back to ER)
TGN - sorts proteins into different types of vesicles (diff destinations)

89
Q

Golgi Function

A

Processing plant
- sorts
- modifies
- ships (vesicles)
- synthesis of polysaccharides and modification of proteins and lipids
(glycosylation and proteolytic modification)

90
Q

Coat Proteins

A

COPI (retrograde/reverse), COPII (anterograde/forward)
- helps form vesicles
- helps select “cargo”

91
Q

Regulated and constitutive secretory pathways

A

Constitutive (continual) - mucin secretion
Regulated - insulin and neurotransmitter release

92
Q

Lysosomes

A
  • digestive organelles
  • 25 nm to 1 (weird u)m
  • internal pH or 4.6 (proton pump or H+-ATPase regulated)
  • contains hydrolytic enzymes (acid hydrolases)
  • membrane has glycosylated proteins that act as a protective lining against acidic lumen
93
Q

Coatomers

A

Clathrin and AP complex - AP/clathrin coated vesicles move from TGN to other vesicles and help form endocytic vesicles to move from PM to endo/lysosomes

94
Q

Autophagy

A

normal dissembly of unecessary or disfunctional cell components (organelle turnover) by lysosomes

95
Q

Degredation (lysosomes)

A

recycling of PM components and destroying pathogens (only in phagocytic cells)

96
Q

Lysosome Functions

A

Autophagy and degredation of internalized material

97
Q

Plant Vacuoles

A

Intracellular digestion - regulate cytoplasmic pH (pH about 5) acid hydrolases
- sequestration of toxic ions
Mechanical support - regulate turgor
Storage - store amino acids, sugar, CO2 in form of malate, and chemical storage (anthocyanin)

98
Q

Cytoskeleton Function

A

1) structural support
2) spatial organization within cells
3) intracellular transport
4) contractility and motility

99
Q

Components of the Cytoskeleton

A
  • Microfilaments (MF)
  • Microtubules (MT)
  • Intermediate filaments (I)
100
Q

Microtubules (MT)

A

Polymer of alpha-tubulin and beta-tubulin

101
Q

Types of Microtubules

A

Axonemal MT:
- highly organized and stable
- part of structures involves in cell movement
Cytoplasmic MT:
- loosely organized and unstable
- located in cytosol

102
Q

MT assembly/disassembly

A
  • rapid turnover of MTs in vivo
  • shrinking occurs rapidly at plus end (catastrophe)
  • formation if MT is regulated
  • MTOC is central site of MT assembly
103
Q

MT Proteins (MAPs)

A
  • modulate assembly (MAP2 or Tau)
  • mediate interaction with other cells (vesicles/organelles)
104
Q

Classes of MAPs

A

1) Non Motor MAPs - control MT organization in cytosol (Tau)
2) Motor MAPs - kinesin and dynein
- use ATP to generate force
- can move material along MT tract
- can generate slide force between MTs

105
Q

Non motor MAPs

A

Control MT organization in cytosol
- stabilize MTs
- stimulate assembly

106
Q

Defects in Tau

A
  • cause neurofibrillary tangles
  • cause alzheimer’s disease
107
Q

Motor MAPs

A
  • power intracellular transport
  • kinesin (+end directed)
  • dynein (- end directed)
    They move along MT
  • can generate a sliding force btw MTs
108
Q

Kinesin and i Dynein in Zebrafish

A
  • survival mechanism
  • in dark melanin granules are dispersed outward by kinesin (appears darker)
  • in light melanin granules are aggregated forward by dynein (lightly coloured)
109
Q

MTOC

A

Central site of MT assembly
- only in euk cells
2 types:
1) basal bodies (cilia, flagella)
2) centrosomes (spindle formation)

110
Q

Actin Molecules

A
  • central component of MFs
  • monomer: G-actin or globular
  • polymer: F-actin or fibrous
    Actin binds and slowly hydrolyzes ATP
111
Q

Intermediate Filaments

A
  • arrangement of non fibrous alpha helical proteins
  • non polar
    provides structural support and mechanical strength
  • stable compared to MTs and MFs
  • not used in transport
112
Q

Microfilaments

A
  • double helix of actin monomers
  • maintains cell shape
  • cell movement
  • vesicle transport
  • muscle contraction
  • cytokinesis
113
Q

Actin Associated Motor Proteins

A

Myosins (motor proteins):
- primarily move towards the + end of MF
1) conventional myosins: type 1, for muscle contraction
2) unconventional myosins: type 1 and type III-XVIII
- generate force
- contribute to motility in non muscle cells (lamellipodium/push)
(pull)

114
Q

Functions of the Nucleus

A
  • storage repair and replication of genetic material
  • expression if genetic material (transcription, RNA splicing)
  • ribosome biosynthesis
115
Q

Nuclear Lamina

A
  • made of lamins (intermediate filaments) only found in animals cells (the lamin)
  • bound to inner membrane
  • provide structural support for nuclear envelope
  • attachment sites for chromatin
116
Q

Nuclear Pore complex

A
  • composed of NUPs (nucleoporins)
  • octagonal symmetry/basket like
  • projects into cytoplasm and nucleoplasm
    Transport:
  • passive: under 40 kDA, rapid, 100 molecules/minute/pore
  • regulated: larger molecules, slow, 6 molecules/minute/pore