Use LEFT and RIGHT arrow keys to navigate between flashcards;
Use UP and DOWN arrow keys to flip the card;
H to show hint;
A reads text to speech;
25 Cards in this Set
- Front
- Back
Which organelles are competent to take up newly synthesized proteins? (5)
|
ER, Mitochondria, Chloroplast, Peroxisome, Nucleus
|
|
Three compartments contain their signal within the N-terminal. (3)
What else is special about these signals? |
ER, Mitochondria, Chloroplast
Signals are cleaved. |
|
Nature of ER signal
|
6-12 hydrophobic a.a.
|
|
Nature of Mitochondria signal
|
3-5 non-consecutive Arg/Lys
|
|
Nature of Chloroplast signal
|
rich in Serine and Threonine
|
|
Where is the location of the signal for peroxisomal proteins?
|
C-terminal
|
|
Nature of Peroxisome signal
|
Ser-Lys-Leu
|
|
Where is the location of the signal for Nucleosomal proteins?
|
Internal
|
|
Nature of Nucleosomal signal
|
basic a.a.
|
|
Is the signal sequence removed in the peroxisome and the nucleus?
|
No.
|
|
Topogenesis refers to:
|
Targetting of protein due to a specific sequence
|
|
Three types of sequences:
|
Signal sequence
Membrane anchor sequence Sorting sequence |
|
What is a sorting sequence?
|
Target to a specific membrane layer
|
|
Signal sequence
|
Target to a specific organelle.
|
|
Verification of existence of signal sequence: (2 methods)
|
Delete sequence and observe membrane
Place sequence onto a cytoplasmic protein and observe where the protein ends up. |
|
Conformation of protein before integration occurs: (2 methods)
|
Intrinsically (nascent chain synthesis) - co-translational
Chaperones - post-translational |
|
Cytosolic movement towards membranes: (how?)
|
Driven by diffusion
|
|
Recognition of protein onto proper organelle mediated by what type of surface structure?
|
Specific organelle surface receptor.
|
|
Does the receptor have high affinity for the membrane protein?
|
If there was high affinity, then the protein would be stuck on the receptor.
|
|
Channel proteins must maintain aqueous environment.
|
Metabolites cannot leak through, thus channels must be dynamic and gate against leakage of small molecules.
|
|
Where does the energy come from protein translocation? (4)
|
1)- ATP + GTP hydrolysis
2)- Electrochemical/Proton gradient 3)- Chaperones (ATP-dependent) 4)- Folding into final protein conformation |
|
At which stage, does the protein fold into its final conformation?
|
When it has reached the opposite side of the membrane.
|
|
Which cellular location does the s.s. get cleaved?
Why? (two hypothesis) |
Removed on trans side of membrane.
Maintains unidirectionality, S.s. might have kept protein in partial unfolded state. |
|
How are proteins inserted into the membrane?
|
Coupled to translocation across membrane.
When channel reaches a membrane anchor sequence, it will insert into membrane. |
|
What is the structure of a transmembrane domain in a protein?
|
Helix of 20 hydrophobic amino acids.
|