PPT-Richard Flashcards

1
Q

2 types of metabolism

A

Catabolism and anabolism

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2
Q

What is catabolism?

A

Energy-releasing, carbon-oxidising and degradative

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3
Q

What is anabolism?

A

Energy-storing and biosynthesis

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4
Q

What is a futile cycle?

A

When two biochemical reactions run simultaneously, expending a lot of energy

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5
Q

What are the two types of control?

A

Internal and external

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6
Q

What are the two types of control?

A

Internal and external

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7
Q

What is internal control?

A

Participants on the pathway itself accept how it progresses

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8
Q

What is external control?

A

Factors form elsewhere affect the pathways progress

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9
Q

What is external control?

A

Factors form elsewhere affect the pathways progress

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10
Q

What is negative feedback?

A

Inhibition of a process by presence of large amounts of final product (sending the message that the process has produced enough product

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11
Q

What is precursor/reactant activation?

A

Activation of a process by the presence of large amounts of initial reactant (sending the message that the process hasn’t consumed enough reactant)

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12
Q

Types of mechanisms

A

Indirect allosteric mechanisms
Direct mechanisms

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13
Q

What is allosteric control?

A

Regulator molecule binds to the enzyme at a different site that the one to which the substrate binds to altering enzyme conformation

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14
Q

Common form of allosteric control?

A

ATP & AMP

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15
Q

What is direct inhibition?

A

Inhibitor competes with substrate for the active site

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16
Q

What is the michaelis-menton equation?

A

V = Vmax.([S]/[S] + [Km])

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17
Q

What is the lineweaver-Burke plots?

A

Vmax and Km: 1/V=Km/Vmax.1/[S] + 1/Vmax
AKA
y=mx+c

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18
Q

What is the lineweaver-Burke plots?

A

Vmax and Km: 1/V=Km/Vmax.1/[S] + 1/Vmax
AKA
y=mx+c

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19
Q

What is concept of affinity?

A

The higher the affinity, the less ligand is needed to induce 50% maximal binding

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20
Q

What are signals?

A

Hormones and nerve impulses

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21
Q

What are the hormones that act as signals?

A

Amino acid-derived hormones
Steroid hormones

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22
Q

Properties of amino acid-derived hormones

A

Can’t cross plasma membrane
Initiate intracellular responses
Gene expression

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23
Q

Properties of steroid hormones

A

Hydrophobic (can cross plasma membrane)
Ligands for cytoplasmic receptors
Complex binds to DNA

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24
Q

Types of non-steroids hormone receptors

A

Extracellular regions
Cytosolic regions

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25
Q

What are extracellular regions?

A

Interact with hormones
Series of repeated stretches of hydrophobic amino acids

26
Q

What are cytosolic regions?

A

Interact with transducers
Initiate intracellular responses to signals

27
Q

What are the 3 functional domains in steroid hormone receptors?

A

Binding hormone
DNA binding
Receptor to activate the promoters of gene being controlled

28
Q

What is saturation binding?

A

As hormone concentration rises, concentration of hormone bound to receptor rises until no more can bind

29
Q

What is scatchard plot?

A

Mathematical manipulation allows saturation binding to be expresses as straight line

30
Q

What is an autocrine?

A

A cells signals itself via a chemical signal that it synthesises and responds to

31
Q

What is a paracrine?

A

Chemical signals interact with receptors on nearby cells

32
Q

What is an endocrine?

A

Chemical signals are secreted into the blood and carried to the cells they act upon

33
Q

Definition of signal transduction

A

A basic process in molecular cell biology involving the conversion of a signal from outside the cell to a functional change within the cell

34
Q

What are the 5 major classes of steroid hormones?

A

Mineralocorticoids (increase blood volume & pressure)
Glucocorticoids (promote high blood glucose)
Androgens (development of male sexual characteristics)
Estrogens (development of female sexual characteristics)
Protestagens (maintenance of pregnancy)

35
Q

Where do the receptor proteins sit?

A

In the cytoplasm

36
Q

What is the zinc finger domain?

A

DNA binding domain
4 pairs of cys that pushes out the 13 basic amino acids to zinc
Ligand binding-conformation change in receptor- zinc finger assembly

37
Q

How many zinc fingers does a receptor dimer have?

A

2- stabilises the structure and allows specificity of binding

38
Q

What do the receptors bind to?

A

‘Labels’ identifying genes as targets for transcription factors
2 half sites within the DNA sequence

39
Q

What are the two types of specific response elements?

A

Palindromic-TGTTCT…TCTTGT
Direct repeats-TGACCT…TGACCT

40
Q

What forms the RNA polymerase catalysing site?

A

Two binding sites for the DNA (promoter and enhancer)
Causes a loop

41
Q

What causes electrical or nervous signalling?

A

Because of the concentration gradients that exist across the membrane

42
Q

What do gated channels do?

A

Can bring about changes in the ionic environment in the cell, and cause a cellular response

43
Q

What are the consequences of changes in membrane permeability?

A

Changes in pH or oxidation state
Supplying proteins with ionic co-factors
Supplying cells with energy
Changes in potential difference across membrane

44
Q

What are the different forms of Ca2+ as a signal?

A

Buffered form-bound to soluble or membrane linked Ca2+ buffers
Mineral form- collagen rich matrix onto which crystals of insoluble calcium phosphate are laid

45
Q

What is conformational change?

A

Ca2+ presence with cells rigger changes in enzymatic activity/ protein movement

46
Q

What are regulated discrete localised releases of Ca2+?

A

Signal’s which trigger a range of cellular responses

47
Q

Where does Ca2+ signalling occur?

A

In all eukaryotic cells

48
Q

Flow diagram of Ca2+ system

A

-Stimulation of cell:
Entry of calcium into localised parts of cell and binding of calcium to biological molecules
-Cellular response:
Expulsion of calcium from cell
-Cell recovery

49
Q

Why does the ER have a larger surface area than the plasma membrane?

A

To mop/pump up Ca2+ that has leaked into the cytoplasm and act as a Ca2+ store

50
Q

How many Ca2+ mobilisation systems do cells have?

A

2 parallel systems

51
Q

How many Ca2+ mobilisation systems do cells have?

A

2 parallel systems

52
Q

How is Ca2+ released into the cytoplasm?

A

Channels in the plasma and ER membrane

53
Q

How is Ca2+ removed from the cytoplasm?

A

PMCA pump in PM and SERCA pump in ER membrane

54
Q

What is catabolism?

A

Stimulation of glycogen breakdown signalled by glucagon and adrenaline

55
Q

What is anabolism?

A

Stimulation of glycogen synthesis signalled by insulin

56
Q

What does hyperglycaemia lead to?

A

Excess glycation of proteins and lipids

57
Q

What is dyslipidaemia?

A

Inability of body to deal with excess fat

58
Q

What are two cardiovascular complications of type 2 diabetes?

A

Atherosclerosis-inflammation associated accumulation of fatty/glycated deposit is on interior surface of coronary arteries
Coronary heart disease-blood trapped in the occluded artery closes, causing a coronary thrombosis

59
Q

What are PPARs?

A

Ligand activated transcription factor receptor proteins that change express if genes in order to act as insulin sensitising agents, lower blood glucose and boost anti inflammatory defence