CSF (Protein Synthesis) Flashcards

1
Q

Transcription (Initiation)

A

In the promotor, there’s a TATA box and start point. Transcription factors and TATA box binding protein bind to DNA. RNA Polymerase 2 binds.

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2
Q

Transcription (Elongation)

A

RNA nucleotides added to 3’ end of template strand. Phosphodiester bond.

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3
Q

Transcription (Termination)

A

Transcription of the Polyadenylation signal (AAUAAA) then nuclear enzymes release mRNA.

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4
Q

mRNA Processing

A

Capping: a modified guanine nucleotide is added to 5’ end.
Tailing: Poly-A tail on 3’ end.
Splicing: Introns removed from transcript.
UTR: untranslated regions at 3’ and 5’ ends.

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5
Q

What does capping and tailing do?

A

Facilitate export, confer stability, facilitate ribosome binding once in cytoplasm.

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6
Q

Translation (Elongation)

A

Codon recognition, peptide bond formation (large subunit catalyses), translocation (tRNAs move again). GTP.

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7
Q

What happens to empty tRNAs after translation?

A

They are reloaded in cytoplasm using aminoacyl-tRNA synthetases.

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8
Q

Translation (Termination)

A

mRNA stop codon one the A site is bound by a release factor. The bond between P-site tRNA and last amino is hydrolysed, releasing chain. Hydrolysis of 2GTP.

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9
Q

Primary Structure

A

N terminus = amino end (like 5’)
C terminus = carboxyl end (like 3’)
Covalent bonds btwn amino acids.

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10
Q

6 steps of protein processing and sorting.

A
  1. Polypeptide synthesis begins.
  2. SRP binds to signal peptide.
  3. SRP binds to receptor protein.
  4. SRP detaches, poly.p. resumes.
  5. Signal-cleaving enzyme cuts off signal peptide.
  6. Completed poly.p. folds. A secretory protein (eg.insulin) is soluabilized in lumen while a membrane protein remains anchored to mem.
    Both then go to Golgi for further maturation.
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11
Q

Post-translational modifications

A

Phosphorylation (in golgi or cytosol).

Can confer activity or ability to interact with other molecules or direct to particular locations.

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