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Study of Enzyme Mechanisms • We have studied the mechanisms of peptide bond formation & hydrolysis by an enzyme • Why study mechanisms? – Structure activity relationships → understand protein folding, etc – Understand “superfamilies” – Design enzyme inhibitors: • Correct a metabolic imbalance • Kill an organism: Herbicides/pesticides, antibiotics Diphtheria Toxin • Corynebacterium diphtheriae • ADP-ribosyltransferase • EF + NAD+ → ADP-EF + nicotinamide • Mechanism also present in other toxins – Pertussis, E.Coli • Binding to EF (eukaryotes) blocks translation Active peptide Reaction O NH2 NH2 N N N P N P O O N O N + + R HN N H OH OH OH OH NAD+ EF - His -H+ NH2 N N N N O P P O O N H N OH O OH OH EF-ADP ribose OH R N NH2 + N Potential Mechanisms? O NH2 + O + N EF (Nu:) O O EF OH -OR- OH OH OH OH OH NAD+ O NH2 + O N EF (Nu:) O O EF OH OH OH OH NH2 + N Active Site with NAD+ Bound (1st Step) Hydrophobic interactions Nu: Testing of Mechanism • Role of tyrosine? – Substitute with Phe → small drop in catalytic activity – Substitute with Ala → 105 drop in activity! – likely responsible for substrate recognition (hydrophobic interactions) • Other mutations show small effects • Key residues? • Glu-148 & His-21 – Mutations show large drop in catalytic activity – Glu148Ser 103 drop in activity Plays a role in NAD+ binding 3-point binding? Activates incoming nucleophile Role of Glutamic Acid in the TS? OO O O NH NH 2 ++ N N 2 O HO HO O HO HO N N R R O O Glu148 N N HH N HN H 2 possible mechanisms? • In the absence of EF, hydrolysis of NAD+ will occur – Model the TS & understand how stabilization of TS occurs – Occurs via an SN2 mechanism! O NH2 + N O HO HO O H H Diphtheria Toxin as a Drug? • Few successful inhibitors of the diphtheria toxin have been found • Instead, the toxin’s apoptotic inducing activity has been exploited to kill Cancer cells – Active site is maintained – Alter it’s targeting ability (to cell receptor) – “Target toxin” • Targeting polypeptide + toxic peptide (DT) Cell receptor Cell death Determination of Mechanism? • How do we elucidate a biological pathway or an enzyme’s mechanism? • Biological Methods – genetic engineering – Construction of mutants • Chemical Methods – Construct analogues (recall the use of fluorine in tRNA) – Photochemical methods – Isotopes (stable & radioactive) • OR can use a combination of both methods! Isotopes • Atoms of the same element having different numbers of neutrons & different masses – e.g. 1H, 2H, 3H & 12C, 13C, 14C • Can be used as “markers” → exploit a unique property of isotope & detect using analytical techniques – Radioactivity – NMR activity • Markers can: – Elucidate a biosynthetic pathway – Provide mechansitic (transition state) information * * Early Days - Radioisotopes Stable Isotopes • Commonly used: 2H, 13C, 18O & 15N