Oral Biochemistry Flashcards

1
Q

Define ‘biomineralization’

A

process by which organisms form minerals

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2
Q

Define ‘amorphous biomineralization’

A

Mineral structure doesn’t have regular size, shape or spatial organization

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3
Q

Define ‘crystalline biomineralization’

A

Atoms in mineral are organized in repeated units

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4
Q

How can such complex shapes of minerals form within living organisms?

A

Scaffold - proteins (e.g. collagen) that give a rigid frame on which the mineral can form

Hydroxyapatite - filling material that fills the scaffold frame

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5
Q

Describe the two steps to crystallization

A

1) Nucleation: local region of solvent become saturated with solute, and solute molecule create a stable cluster. Requires molecules to line up just right for crystallization. Rare for complex crystals.
2) Growth: subsequent growth after nucleation has occurred.

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6
Q

T/F - Nucleation is the easy step in mineralization (i.e. takes the shortest)

A

False, takes the longest, and is the difficult step

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7
Q

Describe ‘dissolving’

A

Crystal components becoming integrate with water:

  • Gravity wants precipitates to form
  • Water surrounds the ion to oppose gravity
  • Increase temperature allows water to be “burrowed” by multiple ions; thus, increasing solubility
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8
Q

Define solubility constant (Ksp)

A

Measure of how soluble a substance is

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9
Q

Define Ksp

A

This is the product of the dissolved ion concentrations in solution at equilibrium.

Higher Ksp = Higher solubility

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10
Q

Define saturated solution conditions

A

Ion product = Ksp

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11
Q

Define supersaturated conditions

A
  • Ion product > Ksp

- Precipitation/mineralization favoured

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12
Q

Define undersaturated conditions

A
  • Ion product < Ksp

- Dissolution/demineralization favoured

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13
Q

When does enamel begin to dissolve?

A
  • When hydroxyapatite Ksp = 0.7 mM^2 (very low)
  • HA Ksp increases exponentially with lowering pH
  • Saliva become unsaturated when pH < 5
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14
Q

Define ‘Unit cells’

A

Regular repeated structure of crystals that fit together specifically. All atoms in a unit cell have a specific space and location (other atoms won’t fit there)

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15
Q

What is nucleation?

A

Nucleation is the formation of a critical amount of unit cells that act as template for new crystals to form.

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16
Q

Define matrix protein

A

Template protein to position the atoms to hydroxyapatite.

17
Q

Name functions of matrix vesicles

A
  • Concentrate the intracellular phosphate and calcium
  • Secrete the matrix vesicle to the cell surface
  • Provide high concentration of “supplies” to the crystal growth site
18
Q

List bone composition’s organic and inorganic material

A

Organic material:

  • Cell
  • Collagen
  • Glycosaminoglycans
  • Proteoglycans and proteins

Inorganic material:

  • Hydroxyapatite
  • Calcium carbonate
19
Q

Describe intramembranous ossification

A

Formed directly in loose mesenchyme from an osteoblast-secreting scaffold and matrix vesicles, then calcifying:

  • bone that are constantly under tension
  • Irregular bones (e.g. skull bones)
20
Q

Describe ‘endochondral ossification’

A

Formed from the replacement of a hyaline cartilage model. Primary and secondary ossification centres form:

  • Bones that are needed to perform immediately and are constantly under pressure
  • Long bones
21
Q

Describe osteoclast/osteoblast activity balance

A

Osteoblasts secrete RANKL and a decoy protein (OPG) that binds with the RANKL. If PTH is present, the decoy protein product is blocked. This allows the RANKL to bind with RANK receptors on pre-osteoclasts

  • RANK receptors trigger production and maturation of osteoclasts
  • PTH triggers osteoclast activity, by binding decoy protein (OPG)
  • This ensures that osteoclastic activity only occurs in the presence of active osteoblasts
  • This ensure that osteoblastic activity always matches osteoclastic activity.
22
Q

Clinically, how do you get netloss of bone during inflammation (e.g. alveolar bone loss in root inflammation)?

A
  • Inflammation and bacteria intermediates bind directly to the RANK receptor and activate the RANK cascade, but not through the osteoblasts: Trigger osteoclast activity, disproportionally to osteoblast activity.
  • Since osteoblast/osteoclast activity is so linked, replacement of loss bone is slow and often permanent.