Survey
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Nicotinamide adenine dinucleotide wikipedia , lookup
Multi-state modeling of biomolecules wikipedia , lookup
Inositol-trisphosphate 3-kinase wikipedia , lookup
Restriction enzyme wikipedia , lookup
Beta-lactamase wikipedia , lookup
Alcohol dehydrogenase wikipedia , lookup
Transferase wikipedia , lookup
Lactoylglutathione lyase wikipedia , lookup
Bio200 POGIL Cell Biology Activity 2 – Enzymes How do enzymes work? Schivell NOTES: - His 12, Lys41, and His119 are key parts of the active site (shown in the gray box and expanded below), which is a small part of the enzyme. MODEL 1: Substrate - The substrate is RNA (ribonucleic acid). Enzyme - Phosphorus (P) is most stable with 5 bonds and has about the same electronegativity as C and H. - This enzyme "catalyzes" the reaction shown. REACTION MECHANISM 1. 2. 3. 6. 5. 4. 1 Bio200 POGIL Cell Biology Activity 2 – Enzymes CRITICAL THINKING QUESTIONS: Schivell 1. What biological macromolecule is the enzyme made of? __________________________ 2. Compare panels 1 and 6 of the reaction mechanism (these contain the initial and final states of the RNA substrate). Describe in fewer than 5 words what has changed about the RNA. For the following questions, it is a good idea to circle or annotate the differences you see on the model itself, or to draw arrows indicating formation of new bonds or movements of atoms. 3. In panel 2 compared to 1, what has changed for the... (be as brief but specific as possible) ... substrate? __________________________________________________________ ... enzyme? ___________________________________________________________ 4. In panel 3 compared to 2, what has changed for the... ... substrate? __________________________________________________________ ... enzyme? ___________________________________________________________ 5. a. In panel 4 compared to 3, what has changed for the... ... substrate? __________________________________________________________ ... enzyme? ___________________________________________________________ b. What new molecule is introduced in panel 4? ____________ 6. In panel 5 compared to 4, what has changed for the... ... substrate? __________________________________________________________ ... enzyme? ___________________________________________________________ 7. In panel 6 compared to 5, what has changed for the... ... substrate? __________________________________________________________ ... enzyme? ___________________________________________________________ 2 Bio200 POGIL Cell Biology Activity 2 – Enzymes Schivell 8. In panel 1, find two different types of molecular interactions that help attract and hold the substrate in the enzyme's active site. (Choose from hydrophobic interactions, covalent bonds, hydrogen bonds, and ionic bonds.) Write the name of each interaction and draw an example of the atoms/groups of atoms involved in the boxes below: 9. a. In panel 2, which atom has an unusual number of bonds? _________________ b. Does the substrate in panel 2 have a higher or lower G than in panel 1? _____________ 10. Consider the enzyme's role in the reaction mechanism: a. Describe the "job" of the two histidine (His) R-groups. b. Describe the "job" of the lysine (Lys) R-group. 11. a. The R-groups of the active site are in the same conformation in panels 1 and 6. Can the enzyme catalyze another reaction after it completes this one? Why? 3 Bio200 POGIL Cell Biology Activity 2 – Enzymes Schivell MODEL 2: The wild-type enzyme and the rate at which the reaction proceeds in its presence is shown to the right. Below are three different enzyme mutants. For each, one aspect of the active site's structure is slightly changed. The mutant enzymes are mixed with RNA in solution. The reaction rates are shown underneath each image. WT = 1000 rxns/sec (His12 shifted "up" slightly) (Lys41 is now Met41) Mut1 = 10 rxns/sec Mut2 = 1 rxn/hour (His119 is now Val119) Mut3 = 1 rxn/millenium 12. How does reaction speed change when the active site is changed? _____________________ 13. a. Is the relative position of a specific R-group within an active site important? _________ b. Which mutant helps to answer this question? ________ 14. When the transfer of a proton between the enzyme and substrate is prevented, is the reaction rate changed slightly or dramatically? __________ 15. Even if an R-group (that is part of the active site) does not normally accept or donate protons or other atoms, or form covalent bonds with the substrate, can it be important? Explain. 4 Bio200 POGIL Cell Biology Activity 2 – Enzymes On your own practice questions: The drawing shows the first 2 steps of a 5 step reaction mechanism. The enzyme's peptide backbone is a solid line (except for some atoms shown in detail). The two arrows (A and B) point to the two ends of the enzyme. The two R-groups of the active site, CYS and HIS, are shown in detail. In the first frame, the enzyme's two substrates are shown, NAD+ and a second substrate in the dotted line. Schivell A 1. What type of biological macromolecule is the second substrate (ignore phosphate)? 2. Which end (A or B) is the amino terminus of the enzyme? _____ B 3. Which of the following R-groups would be best suited to be in the "X" location shown in the first diagram? (Circle ONE) Step 1 4. Which terms describe the reaction catalyzed by this enzyme? (Circle ALL that apply) -endergonic - catabolic - spontaneous - ATP-driven 5. In Step 1, how does HIS participate in the reaction? (1 sentence or less) 6. What is transferred between the two substrates during Step 2? Step 2 7. Can the enzyme catalyze another reaction after Step 2? _______ 9. Using the enzyme to catalyze the reaction changes which of the following? (Circle ALL that apply) - ΔG - ΔS - whether it is spontaneous − ΔG (E ) ‡ A 10. If CYS were changed to Valine (see below), how would the rate of catalysis change? Explain in 1-2 sentences. 5