Would you expect new proteins constructed from B-amino acids toprimarily demonstrate a-helix, B-sheet or another type of secondarystructure? Assume the R-groups are the same as the 20 standardamino acids and they all have the same stereochemistry. Clearlyexplain your reasoning

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Jarrod RobelLv2

29 Sep 2019

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1. What is the purpose of boiling your protein samples before loading them into the polyacrylamide gel?

2. At the end of electrophoresis and Coomassie Blue Standing, would you expect a protein mixture to appear as a single protein band or as multiple protein bands in the polyacrylamide gel? Explain your reasoning.

3. GFP and BFP both consist of 238 amino acids, but differ in the identifies of two amino acids. Assume that both of these proteins have been denatured by boiling and denaturing solution, and are negatively charged from treatment with SDS.

Would you expect GFP and BFP to migrate the same distance during electrophoresis? Explain your reasoning.

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Chymotrypsin serves as a catalyst in the "Hydrolysis" of pepdite bonds - found in carboxylic groups of amino acids, which consist of aromatic pedand groups and large hydrophobic groups. Chymotrypsin is also known to serve as a catalyst in the Hydrolysis of "ester - and amide bonds" , found in hydrophobic groups.

1. Would you expect the K_Mof the reactions of Chymotrypsin with the different substrates to have the same value ? explain your reasoning.

2. Would you expect the V_maxof the reactions of Chymotrypsin with the different substrates to have the same value ? explain your reasoning.

3. Would you expect the " pH-dependence " of the "hydrolysis - reactions" of the different substrates to be the same for all substrates ? explain your reasoning.

Chymotrypsin serves as a catalyst in the "Hydrolysis" of pepdite bonds - found in carboxylic groups of amino acids, which consist of aromatic pedand groups and large hydrophobic groups. Chymotrypsin is also known to serve as a catalyst in the Hydrolysis of "ester - and amide bonds" , found in hydrophobic groups. 1. Would you expect the KM of the reactions of Chymotrypsin with the different substrates to have the same value ? explain your reasoning. 2. Would you expect the Vmax of the reactions of Chymotrypsin with the different substrates to have the same value ? explain your reasoning. 3. Would you expect the " pH-dependence " of the "hydrolysis - reactions" of the different substrates to be the same for all substrates ? explain your reasoning.

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Would you expect new proteins constructed from B-amino acids toprimarily demonstrate a-helix, B-sheet or another type of secondarystructure? Assume the R-groups are the same as the 20 standardamino acids and they all have the same stereochemistry. Clearlyexplain your reasoning

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