Lecture 9 Flashcards
what is the dogma of biology ?
DNA -> RNA -> proteins
name some protein modifications
- phosphorylation
- acetylation
- glycolisation
- proteolytic cleavage
- hydroxylation
describe what proteomics consists of, main difference with genomics ?
Study of proteomes and their function ; sequence mapping, 3D structure, protein interactions
Directly specifies physiological states (compared to genomics)
main technique used to measure proteomics (2 methods)
mass spectrometry
- top down : measure intact proteins
- bottom up : cleave protein in short peptides
difference between untargeted and targeted proteomics
1) targeted : presence and quantity of a specific protein -> sensitive
2) untargeted : quantitative + qualitative study of present proteins -> less sensitive
how much does the environment influence the genome VS metabolome ?
genome : almost no influence
metabolome : big influence
what are small molecules ? (metabolites)
- low molecular weight organic compound
- 50-1500 daltons
- include human and microbial compounds
- concetration detectable by modern instrumentation
what is metabolimics ? what is the metabolome ?
- 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.
why do plants have a higher chemical diversity ?
more chemicals because they need them to defend themselves (can’t run away like us)
what is the general concentration range for all metabolites ?
mM to fM
why are metabolites so relevant ?
- biomarkers (signals of diseases)
- most drugs are metabolites
- cofactors to many proteins
how are the time fluctuations between metabolites, proteins, genes different ?
metabolites : huge variability, time fluctuation
Proteins : a little bit
Genes: no variation
NMR (nuclear magnetic resonance) : advantages and drawbacks
+) quantitative, high reproducibility, structure elucidation -> population based studies
-) low sensitivity, signal overlap
how does LC-MS work ?
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
how does mass spectrometry work ?
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