new biological targets by prathyusha .m

2,173 views

Published on

Published in: Technology, Health & Medicine
2 Comments
2 Likes
Statistics
Notes
No Downloads
Views
Total views
2,173
On SlideShare
0
From Embeds
0
Number of Embeds
1
Actions
Shares
0
Downloads
102
Comments
2
Likes
2
Embeds 0
No embeds

No notes for slide

new biological targets by prathyusha .m

  1. 1.
  2. 2. New biological<br /> tARGETS<br /> INDRUG DEVELOPMENT <br />
  3. 3. UNDER GUIDENCE OF<br />GEETHA REDDY<br /> Associate professor<br /> Biotechnology department.<br /> PRESENTED BY<br /> M.PRATHYUSHA<br /> 10T22S0109<br />
  4. 4. CONTENTS<br />Definition<br />Types of targets<br />Mechanism<br />Enzymes<br />Types of inhibition<br />Applications of enzymes<br />Ligand gated ion channels<br />Regulation & structure <br />New biological targets<br />Conclusion<br />
  5. 5. BIOLOGICAL TARGET<br />A biological target is a biopolymer such as a protein or nucleic acid whose activity can be modified by an external stimulus.<br /> The definition can refer to the biological target of a pharmacologically activedrug compound, or the receptor target of a hormone(like insulin). <br />
  6. 6. TYPES OF TARGETS<br />The most common drug targets of currently marketed drugs include:<br /><ul><li> G protein-coupled receptors (target of 50% of drugs)
  7. 7. Enzymes (especially protein kinases)
  8. 8. Ligand-gated ion channels
  9. 9. Voltage-gated ion channels
  10. 10. Nuclear hormone receptors</li></li></ul><li>MECHANISM<br />The interaction between the substance and the target may be:<br /><ul><li> Non-covalent
  11. 11. Reversible covalent- A chemical reaction occurs between the stimulus and target in which the stimulus becomes chemically bonded to the target, but the reverse reaction also readily occurs in which the bond can be broken.
  12. 12. Irreversible covalent - The stimulus is permanently bound to the target through irreversible chemical bond formation.</li></li></ul><li>ENZYMES<br />Enzymesare proteins that catalyze (i.e., increase the rates of) chemical reactions.<br />In enzymatic reactions, the molecules at the beginning of the process, called substrates, are converted into different molecules, called products. <br />Almost all chemical reactions in a biological cell need enzymes in order to occur at rates sufficient for life. <br />
  13. 13. LOCK AND KEY MODEL<br />
  14. 14. TYPES OF INHIBITION<br /><ul><li>Competitive inhibition
  15. 15. Un competitive inhibition
  16. 16. Non-competitive inhibition
  17. 17. Mixed inhibition</li></ul>USES OF INHIBITORS<br />Since inhibitors modulate the function of enzymes they are often used as drugs. A common example of an inhibitor that is used as a drug is aspirin, which inhibits the COX-1 and COX-2 enzymes that produce the inflammation messenger prostaglandin, thus suppressing pain and inflammation. <br />
  18. 18.
  19. 19. BIOLOGICAL FUNCTION<br />Enzymes serve a wide variety of functions inside living organisms. They are indispensable for signal transduction and cell regulation, often via kinases and phosphatases.They also generate movement, with myosin hydrolysing ATP to generate muscle contraction.<br /> Other ATPases in the cell membrane are ion pumps involved in active transport.<br />
  20. 20. INVOLVEMENT IN DISEASES<br />The importance of enzymes is the fact by lethal illness.<br />One example is phenylketonuria.<br /> A mutation of a single amino acid in the enzyme phenylalanine hydroxylase, which catalyzes the first step in the degradation of phenylalanine, results in build-up of phenylalanine and related products. This can lead to mental retardationif the disease is untreated.<br />
  21. 21. APPLICATIONS OF ENZYMES<br /><ul><li>Food processing -- Amylases from fungi & plants
  22. 22. Baby foods -- Trypsin
  23. 23. Fruit juices -- Cellulases & pectinases
  24. 24. Biological </li></ul> detergents -- Amylases & lipases<br /><ul><li> Contact lens -- Proteases
  25. 25. Molecular Restriction enzymes,DNA</li></ul> biology -- ligases & polymerases.<br />
  26. 26. LIGAND-GATED ION CHANNELS<br />Ligand-gated ion channels (LGICs) are ionotropic receptor or channel-linked receptor. <br />They are a group of transmembrane ion channels that are opened or closed in response to the binding of a chemical messenger  such as a neurotransmitter.<br />
  27. 27. REGULATION<br />The ion channel is regulated by a ligand and is usually very selective to one or more ions like Na+, K+, Ca2+.<br />Many LGICs are additionally modulated by allosteric ligands, by channel blockers, ions, or the membrane potential.<br />
  28. 28. STRUCTURE<br />Each subunit of the pentameric channels consist of the extracellular ligand-binding domain and a transmembrane domain. Each transmembrane domain in the pentamer includes four transmembrane helixes.<br />Example: Nicotinic acetylcholine receptor<br />
  29. 29. NEW CELLULAR TARGETS FOR HIV DRUG DEVELOPMENT<br />Science Daily (May 28, 2009) — Focusing HIV drug development on immune cells called macrophages instead of traditionally targeted T cells could bring us closer to eradicating the disease, according to new research from University of Florida and five other institutions.<br />
  30. 30. EMERGING TARGETS FOR DIABETES<br />The two targets protein tyrosine phosphates 1B(PTP-1B) & Glycogen Synthase kinase-3(GSK-3) have emerged as validated targets for treating this disease.<br /> This two targets are studied which plays a key role in insulin signalling pathway as potential targets for development of anti diabetic therapies.<br />
  31. 31.
  32. 32. High Mobility Group A1 Protein - a New Regulator for Peroxisome Proliferator Activated Receptor gamma Transcriptional Repression - Inhibits Inflammatory Gene Response in Human Aortic Smooth Muscle Cells<br />The project aims to identify new nuclear cofactors for PPARgamma (peroxisome proliferator-activated receptor gamma)-dependent gene transcription in human aortic smooth muscle cells (HASMC) in order to develop new PPARgamma-ligands with improved clinical safety to exert deleterious cardiovascular side effects. <br />
  33. 33. New drug targets for squamous cell carcinoma<br />Researchers at Fred Hutchinson Cancer Research Center have discovered a new drug target for squamous cell carcinoma – the second most common form of skin cancer. <br />Scientists have found that a protein called alpha-catenin acts as a tumor suppressor and they also have unlocked the mechanism by which this protein controls cell proliferation.<br />
  34. 34. Scientists discover new drug target for inflammatory bowel disease: cytokine (IL-23).<br />New treatments for illnesses like Crohn's disease and ulcerative colitis are on the horizon. That's because they've identified IL-23, a cytokine used by the immune system to ward off disease, as a major contributor to the inflammation that is the hallmark of these illnesses. With this information, it is now possible to develop new treatments that stop or reduce the damaging effects of IL-23, potentially bringing relief to millions of people with inflammatory bowel disease (IBD) and possibly other inflammatory illnesses as well.<br />
  35. 35. CONCLUSION<br />Biological targets have been vastly used in drug development process. Many R&D companies are in search of new drug targets in biological systems in order to treat various disorders. It is said to be very high demand and scope for biological targets in biotechnology industries.<br />

×