MEDC 603 Fall 20071 Principles of Drug Design  Enzyme Inhibition Basics Example: 1) Statins (I) inhibit HMG CoA Reductase (E); S = HMG CoA; P = Mevalonate.

Slides:



Advertisements
Similar presentations
ENZYMES!.
Advertisements

Enzymes.
Enzymes Part II COURSE TITLE: BIOCHEMISTRY 1 COURSE CODE: BCHT 201 PLACEMENT/YEAR/LEVEL: 2nd Year/Level 4, 1st Semester M.F.Ullah, Ph.D Showket H.Bhat,
Enzymes. What is an enzyme? globular protein which functions as a biological catalyst, speeding up reaction rate by lowering activation energy without.
General Features of Enzymes Most biological reactions are catalyzed by enzymes Most enzymes are proteins Highly specific (in reaction & reactants) Involvement.
Enzymes Have properties shared by all catalysts Enhance the rates of both forward and reverse reactions so equilibrium is achieved more rapidly Position.
Medical Enzymology By Amr S. Moustafa, M.D.; Ph.D. Assistant Prof. & Consultant, Medical Biochemistry Dept. College of Medicine, KSU
Inhibited Enzyme Kinetics Inhibitors may bind to enzyme and reduce their activity. Enzyme inhibition may be reversible or irreversible. For reversible.
Enzyme activity is measured by the amount of product produced or the amount of substrate consumed. The rate of the enzymatic reaction is measured by the.
Factors Affecting Enzyme Activity
Enzyme Kinetics - Inhibition. Types of Inhibition Competitive Inhibition Noncompetitive Inhibition Uncompetitive Inhibition Irreversible Inhibition.
1 Enzymes Enzyme and Digestion film clip Enzyme and Digestion film clip.
Proteins Making Chemical Reactions Possible
Molecule, Gene, and disease Sun. 2 – 3 – 2014 Session 3 Enzymes and enzyme regulation Dr. Muna A. R.
Enzyme Mechanisms and Inhibition
Enzymes O -CO -C Hi, Everybody! Intended learning outcomes(ILO) 1.Compare reversible competitive to non competitive enzyme inhibitors and others acting.
23.6 Enzymes Three principal features of enzyme-catalyzed reactions: 1. For a given initial concentration of substrate, [S] 0, the initial rate of product.
What Are Enzymes? An enzyme is a catalyst in cellular reactions.
Kinetics of Enzyme Reactions Srbová Martina. E + S ES E + P k1k1 k -1 k cat rapid reversible reaction slow irreversible reaction Rate of the conversion.
Enzymes II: Enzyme Kinetics
ENZYMES. Enzymes are proteins that act on a substance called a substrate. enzyme substrate > product In the above reaction the enzyme's active.
Lecture 7-Kumar Enzyme Inhibition-Drug Discovery Aspirin (anti-inflammatory) Penicillin (effective against gram positive bacteria) Sulfonamides (anti-diarrhea)
Allosteric Enzymes • Allosteric enzymes have one or more allosteric sites • Allosteric sites are binding sites distinct from an enzyme’s active site or.
Enzymes & Regulation of Enzymes Catalysts speed up reactions by lowering the activation energy associated with reactions. In the following exergonic reaction,
LECTURE 4: Principles of Enzyme Catalysis Reading: Berg, Tymoczko & Stryer: Chapter 8 ENZYME An ENZYME is a biomolecular catalyst that accelerates the.
2 Enzymes The Hill equation describes the behavior of enzymes that exhibit cooperative binding of substrate 1. some enzymes bind their substrates.
Enzymes Biomolecules that catalyze chemical reactions - Increase reaction rates - Specific Oxidoreductases – catalyze redox reactions Transferases – transfer.
Lipogenesis. Metabolism of cholesterol.
ENZYMES. Enzymes are Catalysts  Catalytic proteins: change the rate of reactions w/o being consumed  Enzymes speed up reactions by lowering the activation.
Chemical Reaction – process that changes one set of chemicals into another set of chemicals The breaking bonds in reactant and the formation of new bonds.
LECTURE 4: Reaction Mechanisms and Inhibitors Reaction Mechanisms A: Sequential Reactions All substrates must combine with enzyme before reaction can.
Chapter 20 Enzymes and Vitamins
Lock and Key Model Enzymes are specific to their substrates Substrate and active site match each other in two ways: Structurally  substrates that don’t.
Enzyme Kinetics Velocity (V) = k [S]
Draw sketch graphs for enzyme activity with a competitive inhibitor present and for a non-competitive inhibitor present.
Rmax and Km (26.4) Constants from Michaelis-Menten equation give insight into qualitative and quantitative aspects of enzyme kinetics Indicate if enzyme.
R max and K m (26.4) Constants from Michaelis-Menten equation give insight into qualitative and quantitative aspects of enzyme kinetics Constants – Indicate.
Enzyme Inhibition (26.4) Inhibition is a term used to describe the inability of a product being formed due to the presence of another substance (the inhibitor)
Investigation of the enzymatic processes depending on the type of reaction.
Biochemical Reaction Rate: Enzyme Kinetics What affect do enzymes and enzyme inhibitors have on enzyme catalysis on a quantitative level? Lipitor inhibits.
6.1 A Brief Look at Enzyme Energetics and Enzyme Chemistry Converting substrates to product requires intermediate states – Intermediates are less stable.
Lesson 5 Enzymes. Catalyst: something that increases the rate of reactions Enzymes are biological catalysts Often ends with –ase Most enzymes are proteins.
Proteins Making Chemical Reactions Possible. ATB Get a Textbook and turn to page 42.
Inhibitors. Candidates should be able to: (a) state that enzymes are globular proteins, with a specific tertiary structure, which catalyse metabolic reactions.
Enzyme Activators Substances that bind with the enzyme and increase its activity.
Atorvastatin Calcium Atorvastatin Calcium is an inhibitor of HMG-CoA reductase used as a cholesterol-lowering medication that blocks the production of.
Pravastatin sodium Pravastatin sodium is an HMG-CoA reductase inhibitor against sterol synthesis with IC50 of 5.6 μM.
Chapter 24 The Organic Chemistry of the Coenzymes,
Amino Acids, Proteins, and Enzymes
ENZYMES 2-4
Microbial Metabolism In Class Activity
Enzyme Inhibition and Drug Action
Biochem (Test 1) 11. Which of the following statements most directly supports the claim that different species of organisms use different metabolic strategies.
Microbial Metabolism In Class Activity
What is a Blood Clot? 9/18/2018 MEDC 604 Anti-coagulants.
Enzyme 4 - the Inhibition Lecture NO: 1st MBBS
HL 8.1 Metabolism.
Bioreactors Engineering
20.5 Enzyme Inhibition The structure of a noncompetitive inhibitor does not resemble the substrate and does not compete for the active site. Learning.
Enzymes.
ENZYMES.
Chapter Three: Enzymes
Patrick: An Introduction to Medicinal Chemistry 6e
Chapter Three: Enzymes
Enzyme Regulation 1.
Enzyme Inhibition and Drug Action
Do Now Take out your: Vocabulary notes + Toothpickase lab
Enzymes.
Presentation transcript:

MEDC 603 Fall Principles of Drug Design  Enzyme Inhibition Basics Example: 1) Statins (I) inhibit HMG CoA Reductase (E); S = HMG CoA; P = Mevalonate 2) I = Warfarin, E = reductase, S = vitamin K epoxide, P = vitamin K Other examples: salicyclic acid, physostigmine, sulfanilamide, captopril, enalapril, finasteride, …… Units of K I and IC 50 = M

MEDC 603 Fall S E + S EE + P  Competitive Inhibition Principles of Drug Design E I I E + S E:S P + E E:I I KMKM k CAT KIKI

MEDC 603 Fall Substrate Inhibitor Design of Statins  Competitive Inhibition …. Example Principles of Drug Design

MEDC 603 Fall  Competitive Inhibition …. Example Principles of Drug Design AZT  potent inhibitor of HIV-RT, the retroviral polymerase which catalyzes the formation of proviral DNA from viral RNA.

MEDC 603 Fall  Non-Competitive Inhibition Principles of Drug Design S E + S EE + P E I S I E + P

MEDC 603 Fall  Non-Competitive Inhibition … Example Principles of Drug Design Bivalirudin Thrombin Argatroban Thrombin Exosite II Exosite I Thrombin Active Site Argatroban H 2 N-D-Phe-Pro-Arg-Pro-Gly-Gly-Gly-Gly-Asn-Gly HOOC-Leu-Tyr-Glu-Glu-Pro-Ile-Glu-Glu-Phe-Asp Bivalirudin Competitive Non-competitive

MEDC 603 Fall Nevirapine  potent inhibitor of HIV-RT … K I ~ nM … no resemblance to any of the natural nucleotide substrates … binds in a hydrophobic binding pocket adjacent to the substrate-binding pocket and modifies the rate of polymerization.  Non-Competitive Inhibition … Example Principles of Drug Design

MEDC 603 Fall  Differentiation of type of inhibition Principles of Drug Design E + S E:S Response E:I E:S:I

MEDC 603 Fall  Irreversible Inhibition Principles of Drug Design E + S E:S E-S No further rxn. Substrate behaves as an inhibitor! aka …. Suicide substrate inhibitors or Mouse trap inhibitors or Trojan horse inhibitors