Lecture 5 Flashcards

1
Q

Chelate

A

Some ligands can form multiple bonds

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2
Q

ligands

A

transitional metals form complexes with molecules or ions

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3
Q

Biuret Reagent

A

Measures total protein by reacting with peptide bonds
most common automated method

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4
Q

Refractive index

A

how much a liquid bends light
Dissolved substances change refractive index

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5
Q

Hemoglobin (Hb)

A

Globular (soluble) protein
Found in red blood cells

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6
Q

What does Hb contain?

A

Contains heme prosthetic groups
Each hemoglobin four heme sites to bind O2
Also participates in CO2 transport

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7
Q

What happens when O2 binds to Hb?

A

Fe2+ -> Fe3+ when O2 binds

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8
Q

Prosthetic groups

A

something extra that is added to a protein that is necessary for its functionality
Heme is an example

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9
Q

Methemoglobin

A

Oxidized form of hemoglobin
Fe2+ -> Fe3+ has occurred without binding O2

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10
Q

Methemoglobinemia

A

High levels of methemoglobin
Blood turns bluish-brown
Treated with methylene blue therapy

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11
Q

Cyanmethemoglobin

A

Methemoglobin can react with CN- to form a very stable compound Cyanmethemoglobin
used to analyze the hemoglobin content of blood

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12
Q

Carboxyhemoglobin

A

Hemoglobin has much higher affinity for carbon monoxide (CO) than it has for O2
HbO2 + CO -> Hb-CO + O2

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13
Q

Le Chatelier’s Principle

A

high [O2] shifts reaction towards HbO2
low [O2] shifts reaction towards Hb + O2

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14
Q

Bohr Effect

A

O2 affinity decreases with increasing CO2
high CO2 triggers the release of bound O2
It is as if hemoglobin “feels” that it should release the O2 when it reaches the cells that need it the most

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15
Q

Haldane effect

A

O2 removal enhances hemoglobin’s affinity for CO2

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16
Q

RBC lifespan

A

120 days

17
Q

What does heme become as hemoglobin degrades?

A

Bilirubin

18
Q

What do the proteins in hemoglobin become when it degrades?

A

Amino Acids

19
Q

Forms of Hemoglobin

A

A1 (A), A2, F (Fetal)

20
Q

Which form of hemoglobin is most common?

A

A1

21
Q

What happens to F hemoglobin in adults?

A

phased out with growth
Fetus -> babies -> adults (less 1 %)

22
Q

Hemoglobinopathies

A

mutant forms of hemoglobin produced

23
Q

Anemia

A

low Hb levels caused by bleeding, RBC destruction, or insufficient production as in thalassemia

24
Q

Thalassemias

A

group of genetic diseases with insufficient production of particular (, , ) globin chains

25
Q

Myoglobin

A

Found in muscles - stores O2
Only has 1 heme (binds 1 O2)

26
Q

Bence-Jones protein

A

protein is found in the urine of many multiple myeloma patients
Should not be in urine