T1 Cells and Molecules Flashcards

1
Q

How can peripheral proteins be removed from a cell membrane?

A

Salt solutions to disrupt ionic bonds, detergent or phospholipases

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2
Q

How many columns of tubulin polymer are arranged together to form a microtubule?

A

13

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3
Q

What is spectrin?

A

A cytoskeletal protein that lines the intracellular side of the plasma membranes. Spectrin helps maintain plasma membrane integrity and cytoskeletal structure

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4
Q

What may be raised in the blood due to tissue damage?

A

ALT, troponin, CK

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5
Q

Which way will kinesin move along a microtubule?

A

In the positive direction

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6
Q

What is the smallest size resolvable by a light microscope?

A

200 nm

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7
Q

What is normal blood volume?

A

5L

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8
Q

What is the diameter of an actin filament?

A

7 nm

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9
Q

Describe linolenic acid.

A

Essential fatty acid C18:3, omega 3

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10
Q

What is sphingomyelin?

A

A phospholipid which has no glycerol backbone

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11
Q

How many actin subunits are there per turn of the double helix?

A

13

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12
Q

Which amino acid is a precursor of adrenaline and dopamine?

A

Tyrosine

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13
Q

What can inhibit acetylcholine esterase reversibly?

A

Neostigmine

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14
Q

What causes Creutzfeldt Jakob Disease?

A

A prion, an infectious pathogen, converts the body’s proteins from normal form to pathogenic form by forming B sheets where there were a-helixes

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15
Q

What size are mitochondria?

A

About 1 um

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16
Q

What shape is the curve in allosteric enzyme control?

A

Sigmoid

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17
Q

What kind of saccharide is galactose?

A

Monosaccharide

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18
Q

What are amyloid proteins?

A

Stable proteins which aggregate to form plaque s

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19
Q

Which enzyme is defective in phenylketonuria, what does this enzyme do?

A

Phenylalanine hydroxylase, converts phenylalanine –> tyrosine

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20
Q

Which organelle does myoclonic epilepsy with ragged red fibres affect?

A

Mitochondria

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21
Q

What happens in Alzheimer’s?

A

Microtubule associated protein, Tau, is hyperphosphorylated and forms neurofibrillary tangles

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22
Q

What do lyases do?

A

Catalyse cleavage of C-C, C-O or C-N bonds

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23
Q

What are lamellipodia?

A

Exploratory processes formed by actin and intergrins

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24
Q

What kind of protein is GABA-A?

A

Membrane ion channel

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25
Q

Is valine polar or non polar?

A

Non polar

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26
Q

Which neurotransmitter is formed from tryptophan?

A

Serotoninin

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27
Q

What is allosteric control of enzymes affected by?

A

The end product

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28
Q

What is the Michealis Menton equation?

A

Vo = Vmax [S]/ Km + [S]

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29
Q

What kind of enzyme is lactate dehydrogenase?

A

An oxoreductase

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30
Q

How does DNA compare to RNA?

A

It has one fewer O2 in each pentose sugar than RNA

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31
Q

Is tryptophan polar or non polar?

A

Non polar

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32
Q

What is the diameter of a microtubule?

A

25 nm

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33
Q

What size are perixisomes?

A

0.5-1.5 um

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34
Q

Which amino acid acts as a neurotransmitter?

A

Glutamate

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35
Q

What kind of enzyme is tryspin?

A

Hydrolase

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36
Q

How many rings does cholesterol have?

A

4

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37
Q

What is an amphipathic constituent of cell membranes?

A

Glycolipids

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38
Q

What enzyme class do kinases fall into?

A

Transferase

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39
Q

Which subunits polymerise to form microtubules?

A

Alpha and beta tubulin

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40
Q

Which way will dynein move along a microtubule?

A

In the negative direction

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41
Q

How can we describe stearic acid?

A

C18:0 a saturated fatty acid

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42
Q

Name an intermediate filament disease.

A

Epidermolysis bullosa symplex

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43
Q

What are the cofactors for cytochrome oxidase?

A

Cu2+ and Fe2+/3+

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44
Q

How does cell movement occur?

A

When actin filaments polymerise and depolymerise rapidly

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45
Q

How thick are cell membranes?

A

5 nm

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46
Q

Name two microtubule diseases.

A

Alzheimers and hereditary spastic paraplegia

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47
Q

What is a normal size for a bacterium?

A

1 um

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48
Q

What are the cofactors for glutathione peroxidase?

A

Se2+

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49
Q

What is the structure of actin?

A

Double helix

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50
Q

What is Kcat?

A

The turnover number, equivalent to the number of substrate molecules converted to product in a unit of time on a single enzyme molecule saturated with substrate

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51
Q

How can anchored proteins be removed from a cell membrane?

A

Phospholipases only

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52
Q

What are the cofactors for carbonic anhydrase?

A

Zn2+

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53
Q

What does taxol do?

A

Stabilise microtubules

54
Q

Describe myoclonic epilepsy with ragged red fibres (MERRF)

A

Mutation of mitochondrial gene for tRNA-lys, disruption of enzymes for oxidative phosphorylation

55
Q

What is a normal size for a virus?

56
Q

Describe palmitic acid.

A

Saturated fatty acid C16:0

57
Q

What is a normal size for a human cell?

58
Q

Which neurotransmitter is formed from histidine?

59
Q

What joins intermediate filaments to actin and microtubules?

60
Q

What charge does the R-group of lysine have?

61
Q

What are some characteristics of Creutzfeldt Jakob Disease?

A

Inital symptoms: difficulty walking, slurred speech, dizzy, numb, vision issues, severe depression, anxiety, withdrawal, irritable, insomnia eventually fatal

62
Q

What is another name for tocopherol?

63
Q

What is Km?

A

Km= k2+ (k-1) / k1 And it represents the affinity of an enzyme for substrate when K2 is negligible

64
Q

What charge does the R-group of glutamate have?

65
Q

When is tyrosine present in low levels and phenylalanine present in high levels?

A

In phenylketonuria

66
Q

Describe linoleic acid.

A

Essential fatty acid C18:2, omega 6

67
Q

Which enzyme is Ni+ a cofactor for?

68
Q

What do pathogenic prions polymerise to form?

69
Q

How big is the nucleus?

70
Q

What is chromatin?

A

A complex of DNA, histones and non-histone proteins in nucleus

71
Q

What is F-actin a polymer of? (filament actin)

A

G-actin (globular actin)

72
Q

What may fibrin have a high proportion of?

A

B-pleated sheets

73
Q

What divides the cell into different functional compartments?

A

Cellular organelles

74
Q

What lowers Vmax?

A

Non competitive inhibitors

75
Q

How does the drug colchicine prevent cell division?

A

Inhibits microtubule polymerisation by binding to tubulin

76
Q

What does polymerisation of actin filaments require?

A

ATP to be bound to actin filament

77
Q

What is produced when you combine glucose and fructose?

78
Q

Which way are collagen helices?

A

Left handed

79
Q

What increases Km?

A

Competitive inhibitors

80
Q

How are intermediate filaments formed?

A

From tetramers linked in a staggered manner

81
Q

How do lamellipodia or filopodia attach to the extracellular matrix?

A

Through the formation of focal adhesions

82
Q

What is Fick’s law?

A

That the maximum size of a cell is limited by rate of diffusion across membrane

83
Q

What are cilia movements associated with?

A

Microtubules and dynein

84
Q

What is the Lineweaver-Burk plot?

A

The inverse of Michealis Menton

85
Q

What kind of secondary structure do fibrillar proteins have?

A

B- pleated sheets

86
Q

Where are phospholipids synthesised?

A

Perioxisomes

87
Q

What happens to axons lacking in intermediate filaments?

A

They are reduced in diameter

88
Q

What are the cofactors for pyruvate kinase?

A

Mg2+ and K+

89
Q

Describe Tay-Sachs disease.

A

Mutation of lysosomal hexosamidase-A enzyme. Causes accumulation of ganglioside which is pathogenic

90
Q

What kind of molecule is cholesterol?

A

Amphipathic

91
Q

What do dyenin and kinesin do?

A

Associated with movement of vesicles along microtubules

92
Q

How do listeria bacteria spread between cells?

A

By causing actin to polymerise behind the bacteria

93
Q

What does phospholipase C do?

A

Cleaves the bond within phospholipids between glycerol molecule and phosphate group

94
Q

What binds to microtubule monomers when it is assembled?

95
Q

What does oxidation of tyrosine produce?

96
Q

Where does ribosomal subunit assembly occur?

A

The nucleolus

97
Q

Where are lipids and steroids synthesised in the cell?

A

Smooth endoplasmic reticulum

98
Q

What charge does the R-group of arginine have?

99
Q

Name two actin associated diseases, which protein is each associated with?

A

Duchenne or Becker muscular dystrophy- dystrophin

Usher’s disease- Myosin VII

100
Q

Where are sterocilia found, how do they work?

A

In the ear, the cells are depolarised or hyperpolarised by deflections caused by sound. Actin filaments keep the sterocilia stable

101
Q

When does Km= [S]?

A

When Vo = 1/2 Vmax

102
Q

What supports the shape of microvilli?

A

Bundles of actin filaments

103
Q

What do peroxisomes do?

A

Breakdown long chain or branched fatty acids and amino acids

104
Q

What do colchcine and vinblastine do?

A

Destabilise microtubules

105
Q

Is rate of diffusion proportional to distance to diffuse?

106
Q

When are hexoses labelled alpha?

A

When the -OH group falls below the anomeric carbon

107
Q

Which organelle does Hutchinson-Gilford progeria effect?

A

Cell nucleus

108
Q

What does amphiphatic mean?

A

Both hydrophilic and hydrophobic

109
Q

Where is 1/Vmax on the Lineweaver Burk plot?

A

At the intercept of the y-axis

110
Q

What enzyme class do dehydrogenases fall into?

A

Oxoreductase

111
Q

What enzyme class do lipase and sucrose fall into?

A

Hydrolases

112
Q

Which amino acid is necessary for skin pigmentation?

113
Q

What is profilin?

A

An actin sequestering protein

114
Q

What is the smallest size resolvable by an electron microscope?

115
Q

Which organelle does Zellweger syndrome affect?

A

Perixisomes

116
Q

What is the Golgi?

A

A structure with cis and trans faces which creates lysosomes as well as packaging proteins from the endoplasmic reticulum

117
Q

What is ankyrin?

A

Ankyrins are a family of adaptor proteins that mediate the attachment of integral membrane proteins to the spectrin-actin based membrane cytoskeleton

118
Q

What size are lysosomes?

119
Q

How does Oubain work?

A

It is a cardiac glycoside which inhibits Na+/K+ATPase so there is a higher concentration of Na+ inside the cell. this inhibits Na+/Ca+ so less Ca2+ is pumped out and intracellular Ca2+ increases

120
Q

What kind of protein is Ras?

A

Anchored membrane protein

121
Q

What is the cytoskeleton made of?

A

Actin, intermediate filaments, microtubules

122
Q

Which organelle does Tay-Sachs disease effect?

123
Q

What are the 4 classes of phospholipase and what do they do?

A

PLA1 and PLA2- break ester bonds between fatty acid and glycerol.
PLC- breaks phosphate to glycerol bond
PLD- breaks bond of polar group to phosphate

124
Q

What is transgelin?

A

A cross linking protein which binds actin

125
Q

Which enzyme is deficient in lactose intolerance?

A

Lactase or B-galactosidae

126
Q

Which enzyme is Mg+ a cofactor for?

A

Hexokinase, G-6-phosphatase, pyruvate kinase

127
Q

Which neurotransmitters are formed from tyrosine?

A

Adrenaline, dopamine

128
Q

Describe Hutchinson-Gilford Progeria.

A

Mutation in lamin A part of nuclear envelope, distorts shape of nucleus (blebbed) production of unique progerin protein

129
Q

Name 4 intermediate filaments.

A

Keratin, vimetin, neurofilamin, glial fibrillary acidic protein

130
Q

How can intergral proteins be removed from a cell membrane?

A

Detergent or phospolipases