Week 3 - Tetrahydrofolate, Vit. B12, and S-Adenosylmethionine - Skildum Flashcards

1
Q

What is the most common source of methyl donation?

A

Serine! You got this!

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2
Q

Why is folate important for pregnancy?

A

Folate deficiency is associated with Spina Bifida. (a neural tube defect that has very sad effects)

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3
Q

What is the cause of Hereditary folate malabsorption?

A

It is inhertied mutation of the Proton Coupled Folate Transporter gene. (SLC46A1)

SO even if you eat enough folate, you’ve got deficiency. (This is the deficiency that we saw in our case study!)

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4
Q

The enzyme responsible for reducing both folate to dihydrofolate and dihydrofolate to teatrahydrofolate?

A

Dihydrofolate reductase

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5
Q

What drugs use Dihydrofolate reductase (DHFR) as a drug target?

A

Methotrexate (cancer/ rheumatoid arthriris)
Trimethoprim (antibacterial)
Primethamine (antimalarial)

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6
Q

Tryptophan, Threonine, Isoleucine, Lysins, Leucine, Phenylalanine, and Tyrosine can all be degraded to which ketone body?

A

Acetoacetate

not sure if this is important

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7
Q

What are the BASIC oxidation states of THF?

A

1: THF
2: 10-Formyl-THF
3: 5,10-Methenyl THF
4: 5,10-Methylene THF
5: 5-Methyl THF

The numbers are referring to what is either bound to the 5’ or 10’ nitrogen

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8
Q

THF can be directly converted to 10-Formyl THF by using what source of carbon?

A

Formate

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9
Q

IF histidine is used by THF as the methyl donor, what step of the THF cycle does it enter?

A

It skips right to the 5,10-Methenyl THF

This is after a 5-formimino THF intermediate

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10
Q

What step of the THF reaction is IRREVERSIBLE? Why is this significant?

A

The reduction of 5,10-Methylene THF to 5-Methyl THF.

It is referred to as the “methyl trap.” This is because 5-Methyl THF’s ONLY metabolic fate is to combine with cobalamin to produce methylcobalamine. When there is no B12 (cobalmine), the 5-methyl THF is jsut stuck and can’t do any other methyl trasnfer reactions.

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11
Q

Why do you get neurological problems with Vit B12 dietary or functional deficiency?

A

Vitamin B12 is necessary to the process of creating SAM (s-adenosylmethionine). Sam is then used to donate methyl groups to many substrates.

LIKE neurotransmitter precursors.

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12
Q

When using serine as a source of carbon donation, which step of the THF process does it enter?

A

Serine and THF create:

5,10-Methylene THF

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13
Q

Thymidine (nucleotide), purine bases, methionine, and s-adenosyl methionine (SAM) are ALL products of what kinds of reactions?

A

Carbon donation reactions!

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14
Q

IN the case of folate deficiency, why would magaloblastic anemia be a problem?

A

Blood cells divide rapidly becuase there is such a high tunrover rate. This kind of division requires a lot of deoxynucleotides to synthesize DNA. When these nucleotides are unavailable the cell continues to grow until they are, which results in gigantic RBC’s. Not cool.

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15
Q

Why is methotrexate an effective cancer drug?

A

It inhibits DHFR (dihydroxyfolate reductase). This is the enzyme that converts FH2 to FH4 and making it part of the process of converting dUMP to dTMP (Thymine). So stopping the creation of DNA, stops all of the fast replicating cells (prominent in cancer). Also gives unfortunate side effects of chemo.

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16
Q

Why is 5-Fluooracil an effective cancer drug?

A

It inhibits thymidylate synthase. This is the reaction converting dUMP to dTMP (Thymine). BY inhibitng DNA production, you inhibit the fast-replicating cells. (This is how cancer cells usually are, so it targets them in particular)

17
Q

Why can Vit B12 deficiency have such similar effects as folate deficiency??

A

For biosynthetic pathways, carbon is not donated DIRECTLY from N5-methyl FH4. First it is donated to homocysteine (a rxn requiring B12) to make methionine. Then an adenosine base is added to make SAM. SAM is then used to add methyls for biosynthetic rxns.
(So without B12, its the same is if you didn’t have folate)

18
Q

What is the usefulness of adenosylcobalamin?

A

Catalyzes the rxn converting methylmalonyl-CoA to Succinyl-CoA.

CONNECTION from past material:
Catabolism of branched or odd-chain fatty acids creates: methylmalonyl CoA

Back to the TCA cycle!

19
Q

Let’s talk about Vitamin B12 absorption:

Try to give the main bulletpoints of the process :)

A
  • B12 first attaches to R-binders in the stomach
  • R-binders are digested off by proteases
  • B12 is then bound to intrinsic factors secreted from parietal cells
  • B12/intrinsic factor complex taken up in intestines
  • Tranported through the blood complexed to transcobalamin II protein
  • Stored in the liver with cubillin
20
Q

What is pernicious anemia?

A

megaloblastic anemia and neuropathy (pain and numbness in the extremities)

21
Q

Why could autoimmune destruction of parietal cells cause pernicious anemia?

A
  • Parietal Cells are what secrete intrinsic factors
  • Intrinsic factors usually complex with Vit B12 to allow it to be taken up in the blood by transcobalamine II protein
  • An absorption problem of B12 is going to produce pernicious anemia
  • BECAUSE b12 usually helps catalyze the conversion of FH2 to FH4, which goes on to make thymine
22
Q

Hyperhomocysteinemia can cause cardiovascular and neurological problems. Describe how this problem can occur.

A

1) mutation in methionine synthase. This catalyzes the trasnfer of methyl from methylcobalamin to turn homocystein into methionine
2) Cobalamine deficiency
3) Vit. B6 (PLP) deficiency. Important for converting homocysteine to Cystanthionine, and then Cystathionine to Cysteine.