3. A mixture of proteins shown in the table below are dissolved in water and injected into a size exclusion chromatography system. Given the calibration curve for the SEC column, draw a qualitative curve to show the expected results (chromatogram) of running the SEC by showing detection units (RI or UV absorbance) on the y- axis and time on the y-axis. Relative peak heights (areas under curves) and times should be as quantitative as possible. ID 1 2 3 4 5 6 Protein Collagen Lactoperoxidase Insulin Fibronectin Lysozyme Trypsin Molecular Weight 68,000 92,600 5,800 55,000 16,000 47,000 Note: as shown in the calibration curve, the beads in the column can separate molecules less than ~120,000 molecular weight, but any proteins larger than that will elute at ~5 minutes. The minimum molecular weight that can be separated in the column is is 20,500; smaller proteins elute at 25 minutes. The equation of the calibration curve is shown on the graph. Conc pl 0.5 g/L 1 g/L 12 g/L 5 g/L 2 g/L 10 g/L log(Molecular Weight) 8 65432 7.8 6.5 Type fibrous a-helices; structural antibacterial enzyme globular protein fibrous protein 7.3 4.6 4.6 cell-lysing enzyme 2.5 digestive enzyme Calibration Curve for SEC Column 3log (MW) = 5.262 -0.0378t R² = 0.9991 10 20 Elution Time, min 30

Biochemistry
9th Edition
ISBN:9781319114671
Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.
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Chapter1: Biochemistry: An Evolving Science
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A qualitative graph!
3. A mixture of proteins shown in the table below are dissolved in water and injected into a size exclusion
chromatography system. Given the calibration curve for the SEC column, draw a qualitative curve to show the
expected results (chromatogram) of running the SEC by showing detection units (RI or UV absorbance) on the y-
axis and time on the y-axis. Relative peak heights (areas under curves) and times should be as quantitative as
possible.
ID
1
2
3
4
5
6
Protein
Collagen
Lactoperoxidase
Insulin
Fibronectin
Lysozyme
Trypsin
Molecular Weight
68,000
92,600
5,800
55,000
16,000
47,000
Note: as shown in the calibration curve, the beads in the
column can separate molecules less than ~120,000
molecular weight, but any proteins larger than that will
elute at ~5 minutes. The minimum molecular weight that
can be separated in the column is is 20,500; smaller
proteins elute at 25 minutes. The equation of the
calibration curve is shown on the graph.
Conc
0.5 g/L
1 g/L
12 g/L
5 g/L
2 g/L
10 g/L
log(Molecular Weight)
8765432
pl
7.8
6.5
0
7.3
4.6
4.6
2.5
Type
fibrous a-helices; structural
antibacterial enzyme
globular protein
fibrous protein
cell-lysing enzyme
digestive enzyme
Calibration Curve for SEC Column
3log (MW) = 5.262 -0.0378t
R² = 0.9991
10
20
Elution Time, min
30
Transcribed Image Text:3. A mixture of proteins shown in the table below are dissolved in water and injected into a size exclusion chromatography system. Given the calibration curve for the SEC column, draw a qualitative curve to show the expected results (chromatogram) of running the SEC by showing detection units (RI or UV absorbance) on the y- axis and time on the y-axis. Relative peak heights (areas under curves) and times should be as quantitative as possible. ID 1 2 3 4 5 6 Protein Collagen Lactoperoxidase Insulin Fibronectin Lysozyme Trypsin Molecular Weight 68,000 92,600 5,800 55,000 16,000 47,000 Note: as shown in the calibration curve, the beads in the column can separate molecules less than ~120,000 molecular weight, but any proteins larger than that will elute at ~5 minutes. The minimum molecular weight that can be separated in the column is is 20,500; smaller proteins elute at 25 minutes. The equation of the calibration curve is shown on the graph. Conc 0.5 g/L 1 g/L 12 g/L 5 g/L 2 g/L 10 g/L log(Molecular Weight) 8765432 pl 7.8 6.5 0 7.3 4.6 4.6 2.5 Type fibrous a-helices; structural antibacterial enzyme globular protein fibrous protein cell-lysing enzyme digestive enzyme Calibration Curve for SEC Column 3log (MW) = 5.262 -0.0378t R² = 0.9991 10 20 Elution Time, min 30
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