Protein Synthesis pt. 3 Flashcards

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1
Q

Does the synthesis of all proteins begin on cytoplasmic ribosomes?

A

Yes

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2
Q

Which types of proteins complete synthesis on ER bound ribosomes?

A

Membrane
Secretory
and Lysosomal proteins

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3
Q

What determines the site of protein localization?

A

Signal contained in the primary structure of the protein.

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4
Q

What signal targets a protein for the nucleus?

A

Lys-Lys-Lys-Arg-Lys

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5
Q

What signal targets a protein for the membrane and/or secretion?

A

20-30 AA signal sequence with a string of hydrophobic AAs.

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6
Q

What signal targets a protein to the lysosome?

A

Mannose-6-phosphate

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7
Q

What protein binds to the secretory, membrane, and lysosomal proteins during translation to target them to the rough ER.

A

SRP. Signal recognition protein.

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8
Q

Where do proteins go as they are synthesized on the rough ER ribosomes?

A

They are translated INTO the lumen of the ER via a channel called Sec61.

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9
Q

How do membrane-spanning proteins get translated?

A

Translocated to rough ER to make the bit inside the ER lumen until a stop transfer sequence (about 50% through) is reached causing the remainder of the protein to be translated in the cytosol.

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10
Q

Where does glycosylation of asparagine occur?

A

ER

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11
Q

What does peptidyl prolyl isomerase do?

A

Helps fold proline-rich regions

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12
Q

What does protein disulfide isomerase do?

A

Promotes native conformation of disulfide bonds

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13
Q

What is O-linked glycosylation and where does it happen?

A

Glycosylation of Ser/Thr residues that occurs in the golgi apparatus

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14
Q

How is M6P added in the cis golgi to target lysosomal proteins?

A

Mannose + phosphorylated sugar

then subtract sugar

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15
Q

Fabry’s disease is caused by a defect in what?

A

alpha-galactosidase A resulting in misfolded globosides which then accumulate in lysosomes.

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16
Q

Describe the PDH mutation.

A

Arginine to proline mutation in pyruvate dehydrogenase (PDH) E1alpha subunit causes it not to be imported efficiently into the mitochondria

17
Q

How small do molecules have to be to enter the nucleus by free diffusion?

A

Less than 5000 d

18
Q

What are Nups?

A

Nucleopyorins. FG nups (Phe-Gly) form the diffusion barrier and bind transport receptors to enter the nucleus. Also form the nuclear basket.

19
Q

What is the nuclear lamina?

A

An amorphous stabilizing structure just below the nuclear envelope.

20
Q

What causes Progeria?

A

A defect in nuclear lamins that causes premature aging