Lecture 6 Flashcards

(43 cards)

1
Q

anti-bacterial

A

amylases, cystains, histains, mucins, peroxidases

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2
Q

buffering

A

carbonic anhydrases, histains

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3
Q

digestion

A

amylases, mucins

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4
Q

mineralization

A

cystains, histains, proline-rich proteins, statherins

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5
Q

lubrication and viscoelasticity

A

mucins, statherins

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6
Q

tissue coating

A

amylases, cystains, mucine, proline-rich proteins, statherins

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7
Q

anti-fungal

A

histains

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8
Q

anti-viral

A

cystatins, mucins

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9
Q

properties of mucin that contribute to saliva

A

large size, viscosity, contain lots of glycosylation, provides barrier against pathogens

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10
Q

shear rate

A

saliva being moved back and forth by force

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11
Q

lower shear rate

A

when saliva is at rest, more viscous, good for coating surfaces

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12
Q

higher shear rate

A

when saliva is moving, like in chewing, becomes less viscous and becomes good for moving/dissolving food

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13
Q

netonian fluid

A

a fluid whose viscosity is constant, even when flowing

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14
Q

non-newtonian fluids

A

a fluid whose viscosity changes when applied forces change

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15
Q

shear thinning

A

viscosity decreases when force is applied to the fluid

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16
Q

xerostomia

A

lack of saliva production, caused by aging, medications, diseases, drug abuse, or radiotherapy

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17
Q

saliva orthana

A

mucin-based saliva substitute, behaves like a newtonian fluid, not like natural saliva (non-newtonian fluid)

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18
Q

carboxymethyl cellulose

A

what many commercial saliva substitutes are made of, chemically modified form of cellulose. behaves as a newtonian fluid but is good for lubrication

19
Q

classical and contemporary reasons for sub-cellular fractionation

A

yield, activity, specific activity

20
Q

differential centrifugation

A

cells are distributed in a homogenizer and the resulting mixture, called the homogenate, is centrifuged in a step-by-step fashion of centrifugal force

21
Q

size based separations: dialysis

A

protein molecules are retained in the dialysis bag whereas small molecules diffuse into the surrounding medium

22
Q

size based separations: centrifugal concentrators

A

centrifugal force pushes solution through a membrane with size selective pores. useful for concentrating, desalting proteins

23
Q

size based separations: gel filtration chromatogrophy

A

higher resolution separation than dialysis, smaller proteins experience a higher mobile phase volume becaues they are able to enter pores of the stationary phase beads

24
Q

gel filtration chromatography resolution

A

depends on factors including bead diameter, pore size, salt concentration, column volume, and flow rate

25
pH>pI
protein will be negatively charged
26
pH
protein will be positively charged
27
cation exchange
positive charged proteins will bind to it because it is a negative molecule
28
anion exchange
negatively charged proteins will bind to it because it is a positive molecule
29
ion exchange chromatography
select buffer that is in between the two isoelectric points of the proteins that are trying to be seperated
30
cation exchange in ion exchange chromatography
positively charged proteins will bind to the column, negatively charged proteins will pass through
31
anion exchange in ion exchange chromatography
negatively charged proteins will bind to the column, positively charged ones will pass through
32
separation of hemoglobin
changing the pH of the buffer will separate hemoglobin chains
33
affinity chromatography using antibodies
can purify protein in one step, challenge with this is having a good enough antibody--> producing/identifying an antibody that will only attract the target protein
34
SDS-PAGE
positively charged electrode (at the bottom) will pull proteins through the gel, small proteins will move faster, traveling further down the gel
35
isoelectric focusing
uses gradient of pH--> negative proteins will travel to anode (positive charge) and positive proteins will travel to cathode (negative charge). proteins will migrate to their isoelectric pH, the location where they have no net charge
36
high performance liquid chromatography
a pumping system that pushes solvent through a column packed with small beads (approx. 5 microns) - chromatographic resolution increases as the size of the chromatographic beads decreases - the pressure required to push the solvent (mobile phase) through the packed beads increases as their size decreases
37
reversed phase high performance liquid chromatography
useful means of separating proteolytic peptides using a gradient from low to high percent organic--> helpful for separating intact proteins for structural studies
38
proteomics
- measurements of the proteins in a biological sample - to map protein molecules more precisely in molecular composition across space through time
39
genomics
organismal study of patterns of gene expression related to disease and developmental processes
40
human genome project
all human genes sequenced, approx. 20k human genes
41
functional genomics
effort to make use of the vast wealth of data from the various genomics projects to understand gene and protein functions and interactions - focuses on dynamic aspects of gene transcription, translation, and protein-protein interaction
42
glycomics
study of glycosylation of proteins and lipids on an organismal scale
43
metabolomics
study of the patterns of small molecule metabolites expressed in a biological system