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Chemical Modifications of
Protein
Presented To: Dr. Rafiq Ahmed
Presented By: Zohaib Hussain
1
Protein Engineering
Problem
Solving
Technique
Technology Research
2
Chemical Modifications
Modification
Reactive
Side Chains
Oxidation Reduction Nucleophilic Electrophilic
Natural
3
Deteriorations
Peptide bond scissions
Racemizations
β-eliminations
Formation of products
Reaction of proteins with added chemicals.
4
Why chemical modifications?
• Modified intentionally
• Structure-function relationship
• Studies or for development of new products
• Improved products
• The techniques used in pharmacological, food and feed, or other
industrial areas
5
Sulfhydryl and disulfide
• Catalytic sites of a wide variety of enzymes
• Maintenance
• Inactivation of SH enzymes by iodine
• Modify cysteinyl, tyrosinyl, tryptophanyl
resiudes
• Acidic pH, low temp, and excess of reagent
6
Mechanism
• Human serum albumin and tobacco mosaic
virus
• Ovalbumin ,8-lactoglobulin, dihydrofolate
reductase, and papain
• Oxidation with iodine will led to the formation
of suIfenyl iodide derivatives.
7
Recovery
Sulfenyl derivatives
sulfhydryl
• On addition of thiols
• Recovery of enzymatic activity,
• With the reduction, ranges from 50-100%.
8
Reduction of Protein Disulfide
Bonds
WITH PARTIAL OR TOTAL RETENTION OF BIOLOGICALACTIVITY9
Application in Basic Protein
Chemistry
• Reactive and Active site modifications
• To alter physical and biological properties
• Radio-isotopic labeling
• Modifications for analytical proposes
10
Applications For Food and
Nutritional Purposes
• Blocking of deteriorative reactions
• Physical properties
• Flavor and color
• Nutritional properties
• Aid the physical separation form crude
• Inactivate/remove undesirable substances
11
Blocking of deteriorative
reactions
• Stages harvesting, processing, cooking, storage
• Brown color of bread crust
• Millard reaction (non-enzymatic browning)
• In-solubilize, colored, off-flavours
• Nutritive loss and possibility of toxicity
• Acetylation, methylation, isopropylation
12
Texturization
• Protein rich products-Structure, Shape, texture
• Resemble those of conventional food products
• Meat Like materials from plant proteins-fillers
• Textured proteins- High pH, Substances-
Neutralization-desired physical property
• Recemization-serine
13
Functional Properties
• Gelling ability, solubility, viscosity
• Contribution to nature of food product
• Baking industry-Proteins modified chemically
• Oxidants- Consistency and strength
• Enhance mechanical strength-disulfide
interchanges
14
Application in Pharmaceuticals
• Interaction of proteins-Chemical reagents
• Drug act by direct inactivation of a target
molecule
• Covalent combination with the drug
• Naturally occurring toxins results in the body
• Chemical warfare
15
Life time of drug
• Protein hormones
• Lower their rate of removal from the
bloodstream
• Efficiency/Frequency of admnistration
• Animal insulin by coupling to protamine-zinc
16
Target Specific Transport
• To transport the substances to targets site
• Radioactive iodine or toxic substances attached to
antibodies in attempts to kill cancer cell
• Drugs-irreversible enzyme inhibitors
• Modifications for altering biological properties
• Glutaraldehyde's cross-linking effect on proteins is in
the preparation of prostheses for internal organs, e.g.
heart valves
17
Every Ending is Just a Really New Beginning
23

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Chemical Modifications of Protein and its Applications

  • 1. Chemical Modifications of Protein Presented To: Dr. Rafiq Ahmed Presented By: Zohaib Hussain 1
  • 3. Chemical Modifications Modification Reactive Side Chains Oxidation Reduction Nucleophilic Electrophilic Natural 3
  • 4. Deteriorations Peptide bond scissions Racemizations β-eliminations Formation of products Reaction of proteins with added chemicals. 4
  • 5. Why chemical modifications? • Modified intentionally • Structure-function relationship • Studies or for development of new products • Improved products • The techniques used in pharmacological, food and feed, or other industrial areas 5
  • 6. Sulfhydryl and disulfide • Catalytic sites of a wide variety of enzymes • Maintenance • Inactivation of SH enzymes by iodine • Modify cysteinyl, tyrosinyl, tryptophanyl resiudes • Acidic pH, low temp, and excess of reagent 6
  • 7. Mechanism • Human serum albumin and tobacco mosaic virus • Ovalbumin ,8-lactoglobulin, dihydrofolate reductase, and papain • Oxidation with iodine will led to the formation of suIfenyl iodide derivatives. 7
  • 8. Recovery Sulfenyl derivatives sulfhydryl • On addition of thiols • Recovery of enzymatic activity, • With the reduction, ranges from 50-100%. 8
  • 9. Reduction of Protein Disulfide Bonds WITH PARTIAL OR TOTAL RETENTION OF BIOLOGICALACTIVITY9
  • 10. Application in Basic Protein Chemistry • Reactive and Active site modifications • To alter physical and biological properties • Radio-isotopic labeling • Modifications for analytical proposes 10
  • 11. Applications For Food and Nutritional Purposes • Blocking of deteriorative reactions • Physical properties • Flavor and color • Nutritional properties • Aid the physical separation form crude • Inactivate/remove undesirable substances 11
  • 12. Blocking of deteriorative reactions • Stages harvesting, processing, cooking, storage • Brown color of bread crust • Millard reaction (non-enzymatic browning) • In-solubilize, colored, off-flavours • Nutritive loss and possibility of toxicity • Acetylation, methylation, isopropylation 12
  • 13. Texturization • Protein rich products-Structure, Shape, texture • Resemble those of conventional food products • Meat Like materials from plant proteins-fillers • Textured proteins- High pH, Substances- Neutralization-desired physical property • Recemization-serine 13
  • 14. Functional Properties • Gelling ability, solubility, viscosity • Contribution to nature of food product • Baking industry-Proteins modified chemically • Oxidants- Consistency and strength • Enhance mechanical strength-disulfide interchanges 14
  • 15. Application in Pharmaceuticals • Interaction of proteins-Chemical reagents • Drug act by direct inactivation of a target molecule • Covalent combination with the drug • Naturally occurring toxins results in the body • Chemical warfare 15
  • 16. Life time of drug • Protein hormones • Lower their rate of removal from the bloodstream • Efficiency/Frequency of admnistration • Animal insulin by coupling to protamine-zinc 16
  • 17. Target Specific Transport • To transport the substances to targets site • Radioactive iodine or toxic substances attached to antibodies in attempts to kill cancer cell • Drugs-irreversible enzyme inhibitors • Modifications for altering biological properties • Glutaraldehyde's cross-linking effect on proteins is in the preparation of prostheses for internal organs, e.g. heart valves 17
  • 18. Every Ending is Just a Really New Beginning 23