Lecture 9 Flashcards

1
Q

what is the dogma of biology ?

A

DNA -> RNA -> proteins

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2
Q

name some protein modifications

A
  • phosphorylation
  • acetylation
  • glycolisation
  • proteolytic cleavage
  • hydroxylation
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3
Q

describe what proteomics consists of, main difference with genomics ?

A

Study of proteomes and their function ; sequence mapping, 3D structure, protein interactions

Directly specifies physiological states (compared to genomics)

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4
Q

main technique used to measure proteomics (2 methods)

A

mass spectrometry

  • top down : measure intact proteins
  • bottom up : cleave protein in short peptides
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5
Q

difference between untargeted and targeted proteomics

A

1) targeted : presence and quantity of a specific protein -> sensitive

2) untargeted : quantitative + qualitative study of present proteins -> less sensitive

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6
Q

how much does the environment influence the genome VS metabolome ?

A

genome : almost no influence

metabolome : big influence

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7
Q

what are small molecules ? (metabolites)

A
  • low molecular weight organic compound
  • 50-1500 daltons
  • include human and microbial compounds
  • concetration detectable by modern instrumentation
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8
Q

what is metabolimics ? what is the metabolome ?

A
  • study of metabolites within cells, biofluids, tissues or organisms.
  • complete collection of small molecules (endogenous and exogenous, transient or ven theoretical)
    Its size is not clear.
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9
Q

why do plants have a higher chemical diversity ?

A

more chemicals because they need them to defend themselves (can’t run away like us)

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10
Q

what is the general concentration range for all metabolites ?

A

mM to fM

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11
Q

why are metabolites so relevant ?

A
  • biomarkers (signals of diseases)
  • most drugs are metabolites
  • cofactors to many proteins
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12
Q

how are the time fluctuations between metabolites, proteins, genes different ?

A

metabolites : huge variability, time fluctuation
Proteins : a little bit
Genes: no variation

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13
Q

NMR (nuclear magnetic resonance) : advantages and drawbacks

A

+) quantitative, high reproducibility, structure elucidation -> population based studies

-) low sensitivity, signal overlap

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14
Q

how does LC-MS work ?

A

mobile phase - stationary phase (column) - detector (MS).

Liquid sample introduced before column ; speed of traveling through column will depend on the level of affinity with stationary phase

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15
Q

how does mass spectrometry work ?

A

Sample is ionized -> we measure the mass-to-charge ratio of ionized analytes -> detect the nb of ions at each m/z value -> spectra

Sample can be gas, liquid or solid

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16
Q

how does the time-of-flight mass spectrometer work ?

A

the elements with a lower mass will fly quicker and hit the detector first

17
Q

3 approaches in metabolomics for profiling

A

(un)targeted profiling
Isotopic profiling (labeled elements)
MS imagins : visualize tissues for example

18
Q

what needs to be optimized in targeted and untargeted approaches ?

A

targeted -> front end method (like spectrometer)

untargeted -> bacl end processing (bioinformatics)