Midterm - Hemoglobin Flashcards

1
Q

iron-bearing protein contained within the erythrocytes

A

Hemoglobin

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2
Q

Primary hemoglobin molecule

A

Amino acid sequence

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3
Q

secondary hemoglobin molecule

A

helices & Non helices

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4
Q

tertiary hemoglobin molecule

A

Pretzel like configuration

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5
Q

Quaternary hemoglobin molecule

A

Complete molecule

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6
Q

COMPOSITION OF HEME

A
  • Protophorphyrin IX
  • Ferrous iron (Fe2+)
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7
Q

Heme synthesis first takes place in?

A

Mitochondria

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8
Q

the ability of hemoglobin to bind
or release oxygen

A

Oxygen Affinity

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9
Q

Bohr Effect

A

relationship of O2 affinity with Hb to pH

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10
Q

141 amino acid

A
  • Alpha
  • Zeta
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11
Q

straight line

A

sigmoid curve

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12
Q

Right shift

A
  • Inc. Temp
  • Inc. 2-3 DPG
  • Inc. Hydrogen conc.
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13
Q

Left Shift

A
  • dec. temp
  • dec. 2-3 DPG
  • dec. Hydrogen & CO
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14
Q

Hemoglobin in combination with Oxygen. Gives pinkness to the skin and mucous membrane

A

Oxyhemoglobin

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15
Q

hemoglobin with iron but no O2 seen in venous circulation
unassociated with oxygen

A

Deoxyhemoglobin

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16
Q

Found in normal human embryos and fetuses with a
gestational age of less than three months

A

Embryonic Hemoglobin

17
Q

Composed of 2 zeta and 2 epsilon globin chains

A

Hemoglobin Gower I

18
Q

Composed of 2 alpha and 2 epsilon

A

Hemoglobin Gower 2

19
Q

composed of 2 zeta and 2 gamma

A

Hemoglobin Portland

20
Q

the major hemoglobin of the fetus and newborns

A

Fetal Hemoglobin (HbF)

21
Q

normal adult hemoglobin
* 95 to 97 % of hemoglobin in normal adults produced after
one year onwards
* composed of 2 alpha (141 AA) and 2 beta chains(146 AA

A

Hemoglobin A or A1

22
Q

Constitutes less than 3% of the total hemoglobin
* Composed of 2 alpha and 2 delta

A

Hemoglobin A2

23
Q
  • degradation product of HbA2
  • composed of 2 alpha and 2 delta
A

Hemoglobin A3

24
Q

primary hemoglobin in people with sickle cell
disease

A

Hemoglobin S

25
Q

Glutamic acid is replaced by valine in the 6th position
of beta chain
* SGAVAL

A

Hemoglobin S

26
Q

Hemoglobin C

A
  • CGAL
27
Q

About 2-3% of people of West African descent are
heterozygotes for hemoglobin C

A

Hemoglobin C

28
Q

one of the most common beta-chain
hemoglobin variants in the world.

A

Hemoglobin E

29
Q

an abnormal hemoglobin that occurs in some cases of
alpha thalassemia.

A

Hemoglobin H

30
Q

Are acquired hemoglobin variants whose structure has
been modified by drugs or environmental chemicals.

A

CHEMICALLY MODIFIED HEMOGLOBINS

31
Q
  • Is a form hgb in its ferric state
  • Has a brownish to bluish color and does not revert to red on
    exposure to oxygen.
A

Methemoglobin (HI)

32
Q

Results from the binding of carbon monoxide to heme
iron.
* Hb can combine with carbon monoxide with affinity 200-240
times greater than that of Oxygen.

A

Carboxyhemoglobin

33
Q

Sulfhemoglobin

A

irreversible oxidation of Hb of certain drugs
and chemicals.