Proteomics Flashcards

1
Q

What is a proteome?

A

It is the total set of proteins from a cell, tissue, or organism under a specific condition

Can contain from 10,000 to several billion different proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is proteomics?

A

It is the study of structure, activity, function, modification, localization, and interaction of proteins

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is the most significant impact of alternate splicing of pre-mRNA on the proteome?

A

From one sequence, multiple proteins can form

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What are the four levels of protein structure?

A
  1. Primary
  2. Secondary
  3. Tertiary
  4. Quaternary
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What are the characteristics of primary structure of proteins?

A

This is the amino acid sequence in a polypeptide chain
ex. MTSCYFGHNALTDFL

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are the characteristics of secondary structure of proteins?

A

This level involves the specific structures due to proper folding of the polypeptide chain
ex. a-helix, b-sheet, turns, and loops

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What are the characteristics of tertiary structure of proteins?

A

This is the 3D folding of a polypeptide due to interactions of the secondary structures

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What are the quaternary structure of proteins?

A

This level shows the interaction between different polypeptide subunits

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Why study proteomics?

A
  • Changes in gene or mRNA transcript does not always proportionally translate into fold change of the encoded protein due to mRNA degradation or insufficiency of protein translation
  • Due to alternative splicing, a multi-exon gene may encode different proteins
  • Proteins may have to undergo postranslational modifications such as glycosylation and phosphorylation
  • One protein may carry out multiple functions, and multiple proteins may carry out the same function
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What are the three types of proteomics?

A
  • Expression proteomics
  • Structural proteomics
  • Functional proteomics
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What are some characteristics of expression proteomics?

A

It is the quantitive study of protein expression among different samples (they differ by some variables)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

What are some characteristics of structural proteomics?

A

It is the determination of 3D protein structures on a genome-wide scale and application of structural information for prediction of functions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What are some characteristics of functional proteomics?

A

It is the characterization of the molecular protein network in a cell, tissue or organism

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What equipment is used when conducting proteomics studies?

A
  • Electrophoresis (1D and 2D)
  • Liquid chromotography (FPLC and HPLC)
  • Mass spectrometry
  • Immunoassays
  • X-ray crystallography and NMR spectroscopy
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the steps of proteomics analysis?

A
  1. Sample collection (need to be in cryoprotection if being stored)
  2. Separation of proteins by 2D electrophoresis
  3. Protein characterization
  4. Identification of proteins by MS and other techniques
  5. Data storage and comparison against database for matches
  6. Data analysis using bioinformatics
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the point of separating proteins in proteomics?

A

Helps determine what protein functions are different and network of interactions

17
Q

How does 2D electrophoresis separate proteins?

A

2D electrophoresis separates proteins based on size and charge

Review slide 17

18
Q

What are the advantages of X-ray crystallography for sequencing proteins?

A
  • High resolution atomic structures for proteins
  • Valuable information on protein functions and interactions
  • Essential for structure-based drug design
19
Q

What are some disadvantages associated with X-ray crystallography?

A
  • Time consuming
  • Expensive
  • Special training and equipment (ex. Synchotron)
20
Q

What is the protein microarray?

A

It is a high throughput, miniaturized multi-analyte, solid-phased immunoassay

Thousands of proteins are immobilized on a protein chip

Protein microarrays can generate information on protein interactions and functions

21
Q

What are some free protein databases?

A
  • NCBI (provides protein sequencing information)
  • RCSB (shows positions of sites of interest)
22
Q
A