CELLS Flashcards

1
Q

What’s a chimera?

A

having parts of different origins
e.g. a eukaryotic cell

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2
Q

What’s an endosymbiont?

A

organisms forming symbiotic relationships with another cell/organism

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3
Q

2 types of endosymbiont

A

intracellular
extracellular

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4
Q

what’s a plastid?

A

membrane-bound organelle

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5
Q

How are phylogenetic trees formed?

A

inferred from nucleotide/ amino acid sequence data

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6
Q

most common phylogenetic marker

A

small sub-unit ribosomal RNA (SSUrRNA)

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7
Q

ARCHEZOA hypothesis

A

eukaryogenesis involving exogenous origins of mitochondrion via phagocytosis of an alphaproteobacterium to form mitochondrion

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8
Q

remnant genome of mitochondria
*what does it encode

A

rRNA and protein-coding genes
2 rRNA’s (12S and 16S)
22 tRNA’s
13 essential genes
*encodes sub-units for oxidative phosphorylation enzyme complexes

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9
Q

origins of ER

A

Endogenous

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10
Q

gram-negative bacteria

A

don’t retain crystal-violet stain
- double membrane systems

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11
Q

chloroplast exogenous origin

A

cyano bacteria

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12
Q

plasma membrane functions

A
  • enclose cell content/ separate from environment
  • maintain concentrations of cell substances
  • communication w environment/other cells
  • barrier
  • cell growth/ shape change/ movement/ division
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13
Q

cytosol function

A

protein synthesis/ metabolic pathways

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14
Q

endoplasmic reticulum

A

lipid synthesis/ protein synthesis

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15
Q

golgi apparatus function

A

modification/sorting/packaging of proteins/ lipids

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16
Q

endosome function

A

sorting of endocytosed material

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17
Q

plasma membrane sub-unit
* polarity of parts

A

phospholipid
- hydrophilic phosphate head
hydrophobic fatty acid tails
* amphiphilic!

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18
Q

cholesterol effect on PM

A

decreases membrane permeability to small/ water-soluble molecules
prevent crystallization

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19
Q

4 phospholipids in plasma membrane

A

phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine, and sphingomyelin

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20
Q

function of glycolipid asymmetry

A

extracellular to intracellular signal conversion
charge differences
binding sites
live and dead cell distuinguishment
sugar group addition

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21
Q

self-association of glycolipids

A

H-bonds from sugars / Van der Waals between hydrocarbon chains

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22
Q

oligosaccharides charge and function

A

net negative charge
alters electric field and ion concentrations

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23
Q

lectins

A

carb binding proteins
bind to sugar groups on other glycolipids/ glycoproteins

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24
Q

how is the PM fluid

A

rapid lateral diffusion
flexible hydrocarbon chains
flippases catalyzing movement
cis-double bonds create kinks in fatty acid tail/ shorter tail lengths

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25
temp effect on cis bonds
more cis bonds as temp drops
26
types of membrane proteins
integral peripheral lipid attached
27
when are integral proteins released?
when detergents dissolve PM
28
where are lipid-attached proteins made?
ER prior to cleaving and GPI anchor added via vesicle
29
when are peripheral proteins released?
when protein-protein interaction disrupting agents arrive
30
functions of membrane proteins
transporters linkers receptors catalysis
31
how are transmembrane domains identified?
bioinformatic analysis 'in silico'
32
glycocalyx components
glycoproteins/ glycolipids
33
glycocalyx function
protect cell chemically, physically, biologically adhesion recognition storage affect health and disease
34
glycoprotein links
N-linked O-linked proteoglycans
35
N-glycans
asparagine-linked
36
O-linked
serine/threonine-linked
37
proteoglycans
glycoproteins w GAGs polysaccharide chains covalently linked to a protein core> GPI anchor
38
GAG
glycosaminoglycans
39
ruthenium red
stains carbohydrate layer of glycocalyx
40
detergents
small, amphiphilic molecules of variable structure (more soluble than lipids)
41
detergent behaviour
aggregate to form micelles/ rapidly diffuse in/out affected by temp, pH and salt conc displace lipid molecules affect crystallization/purification
42
tpes of membrane diffusion
rotational lateral
43
how are PM diffusion rates measured
FRAP fluorescence recovery after photobleaching
44
FRAP process
1. mark membrane protein w fluorescent group 2. fluoresecnce group bleached w laser beam 3. time for diffusion measured and diffusion coefficient measured
45
disadvantages of FRAP
can't follow individual protein molecules
46
cortical cytoskeleton
spectrin meshwork maintaining integrity and shape of PM *anaemia doesn't have
47
cell cortex
actin filaments attached to PM
48
cell cortex functions
cell movement endocytosis filopedia production restricts free diffusion of proteins
49
types of active transport
coupled ATP-driven light/redox driven
50
membrane-bending protein function
deforms bilayers (dynamic control of membrane shape)
51
membrane-bending protein mechanisms
insertion of hydrophobic protein domains/ lipid anchors rigid scaffold formation clustering of specific membrane lipids
52
selectivity filter
narrowest region of gated ion channel, limiting rate of passage
53
types of gated ion channels
voltage-gated ligand-gated extracellular ligand-gated intracellular mechanically gated
54
Vmax in relation to gated membrane carriers
rate at which carrier can flip between conformational states
55
Km
concentration of solute when rate of transport is half the maximum value
56
location of nuclear localization signal
at N-terminal end and cleaved after synthesis
57
functions of nuclear pores in envelope
small molecule diffusion dynamic in/out movement export mRNA/ribosome components import structural proteins and gene transcription/ regulation proteins
58
SV40 virus nuclear localization signal
mutation means short sequence is lacking (Thre replacing Lys)
59
nuclear localization signal function
responsible for selectivity of active nuclear import processes
60
how is nuclear localization regulated?
regulated by turning signals on/off via phosphorylation of amino acids close to signal sequences
61
transcription regulator mechanisms
bound to cytosolic proteins either anchored via cytoskeleton/ mask nuclear localization signal gene released by stimuli
62
NF-AT
nuclear factor of activated T-cells
63
what is NF-AT
transcription regulatory protein in cytosol phosphorylated state
64
what are T-cells activated by in NF-AT?
foreign antigen calcium ion concentration increase
65
T cell nuclear activation mechanism
Reacting to the increase in calcium ion concentration, protein phosphatase binds to NF-AT, dephosphorylates and exposes nuclear import signals/ blocks export signal
66
what happens to the NF-AT once in the nucleus ?
activates gene txn of genes required for T-cell activation
67
Use of NF-AT pharmaceutically
used in immunosuppressive drugs when inhibited to block T-cell activation
68
How is the NF-AT response stopped?
Ca2+ concentration decreases NA-FT released from calcineurin re-phosphorylation inactivates import signals and exposes export
69
3 types of cytoskeleton
actin microtubules intermediate filaments
70
actin in plasma membrane
thin, flexible stress fibres maintains cell shape aids surface movement 6-8nm requires ATP to build regulates binding protein
71
actin in cytoplasm
polar, flexible filaments in cortex, found in bundles dynamic polymerisation/ depolymerisation
72
microtubules structure/ location/ formation
25nm diameter tubes made up of tubulins, requiring GTP to build up grow from centrosome
73
microtubules function
motor proteins intracellular movement chr movement in cell division organelle/vesicle shuttling breakdown mitotic spindle
74
intermediate filaments structure
10nm diamter alpha-helical coiled coil assembly regulated by phosphorylation staggered tetramer = 1 filament
75
intermediate filament functions
mechanical strength flexible excess stress prevention tensile force distribution
76
actin functions
cell motility contraction/ adhesion/ mechanosensation
77
actin formation
G-actin monomers added to either end (more rapidly at+) ATP hydrolysis fuels polymerisation actin-binding proteins regulate assembly
78
villi
non-motile actin filaments increasing SA for absorption
79
microtubule assembly
dimers of alpha (-) and beta (+) tubulin formed up of 13 protofilaments via GTP
80
kinesins
motor proteins w head/tail regions globular bind ATP tails bind cargo
81
dyneins
drive cilia/ flagella 9+2 microtubule arrangement bends structure via microtubule sliding
82
cilia
motile numerous/ short aid locomotion microtubules
83
flagella
few/ long aid cell locomotion microtubules
84
intermediate filaments in the nucleus
nuclear lamins (inner membrane meshwork) act as chr/nuclear pore anchorage sites strong > coiled fibrillar protein-packing
85
cytoplasmic intermediate filaments
keratins in epithelia vimentin/ vimentin-related tissue neurofilaments N-/C- terminal domains vary in size
86
examples of vimentin
connective tissue, muscle cells, neuroglial cells
87
nuclear lamins
LMNA/LMNB/LMNC fibrous meshwork of inner nuclear envelope provide structural support cell division breakdown
88
keratin
structural/ mechanical strength in cytoplasm indirect connection via desmosomes
89
myosin I
all cells head/tail intracellular organization moves cargo along actin
90
myosin II
muscle cells dimer filaments contractile
91
spectrin
inner plasma membrane provides mech strength/ stability/ shape link membranes motor proteins / filament systems RBC membranes
92
interphase
normal functions DNA replication for 2 identical chromatids S phase
93
G1
cells produce RNA, enzymes and growth proteins main growth checkpoint
94
G2
cell growth errors corrected tubulin increase checkpoint
95
early prophase
centrosomes replicated prior chromatin coils
96
late prophase
centrosomes to opposite nuclear ends nucleolus dissapears 2 chromatids appear
97
metaphase
centrosome reaches pole spindles appear chromosomes line along equator via centromeres
98
anaphase
chromosomes to opposite poles
99
telophase
nuclear envelope/ nucleolus reformation spindle breakdown cytokinesis chromosomes uncoil
100
Meiosis 1 middle prophase I
synapsis to form bivalents centrosomes to opp nuclear ends
101
Meiosis 1 late prophase I
nuclear envelope breakdown crossing over nucleolus disappears
102
Meiosis I metaphase 1
bivalent alignment spindle forms
103
Meiosis 1 anaphase 1
whole chr movement to poles
104
Meiosis I telophase I
nuclear envelope/ nucleolus reformation cytokinesis
105
meiosis II
mitosis behaviour
106
somatic
non-reproductive cells
107
2 phases of prokaryotic division
replication division (binary fission)
108
4 phases of eukaryotic division
M G1 G2 S
109
G1 checkpoint
assesses size environment favorability DNA damage space availability
110
G2 checkpoint
assesses DNA replication correct DNA cell size environment availability
111
M checkpoint
assesses whether spindles are attached to centromeres
112
CdK
cyclin dependent kinases
113
cyclin-dependent kinases
require cyclins to activate add phosphate from ATP to amino acid in protein differ and destroyed at different checkpoints
114
quiescent state
G0/pause maintenance period reversible/ irreversible depending on cell type
115
PDGF
platelet-derived growth factor
116
FGF
Fibroblast growth factor
117
EGF
epidermal growth factor
118
growth factor concentration
10^-10 M
119
where are growth factors found/ recognised
found in serum receptors in PM
120
apoptosis
cell shrinks nuclear fragmentation apoptotic bodies digested/ recycled
121
necrosis
accidental cell death due to physical/chemical injury
122
necrosis process
cell/ nucleus swells leading to leakage cell lysis triggers inflammatory response
123
2 types of apoptosis triggers
physiological pathogenic
124
physiological activation of apoptosis
used in embryonic development, removing/remodelling tissues homeostasis maintenance cell number control
125
pathogenic activation
viral infection heat shock toxins cytotoxic T cells stressed/damaged cell removal
126
apoptosis activators
hormonal signals cell signalling
127
apoptosis suppressors
survival factors extracellular matrix contact
128
consequences of apoptosis
P53 activation mitochondria leak caspase activation
129
caspase
enzyme, when activated, cleaving nuclear lamins, activating DNAase, cleaving cytoskeleton leaves apoptotic bodies
130
what happens when the cytoskeleton is cleaved?
cells detach from neighbours and lose contact with ECM
131
p53 weight
53KDa
132
p53
transcription factor acting as tumour suppressor
133
DNA damage mechanism
1. damage activates p53 2. p53 blocks progression of cell cycle at G1 checkpoint 3. mitochondrial membrane rupture > cytochrome C leaks between inner/outer membrane 4. cytochrome C in cytosol activates caspases which activate DNAase to cleave lamins and cytoskeletons 5. apoptosis