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  • TITLE
  • CERTIFICATE
  • DECLARATION
  • ACKNOWLEDGEMENT
  • DEDICATION
  • CONTENTS
  • ABBREVIATIONS
  • I. INTRODUCTION AND OBJECTIVES
  • Objectives of the Present Work
  • Organization of the Thesis
  • II. ROLE OF THE POLYMER SUPPORT IN THE SOLID PHASE SYNTHESIS OF PEPTIDES
  • 1. Influence of the degree of cross linking and topographical nature of the polymer matrix
  • 2. Polyacrylamide-type support
  • 3. Polystyrene-polyethylene glycol graft polymers as supports
  • 4. Salvation and swelling of peptide resins
  • 5. Design of new supports with superior swelling properties
  • III. EXPERIMENTAL
  • Materials and Methods
  • 1. Source of chemicals
  • 2. Physical measurements
  • 3. Preparation of reagents
  • a) 4N HCL-dioxane
  • b) Chloromethylmethylether
  • c) Boc Azide
  • d) Preparation of Palladium Black
  • 4. Preparation of amino acid methyl / ethyl esters
  • 5. Synthesis of Boc-amino acids
  • a) Schnabel Method
  • b) 2- (t-butoxycarbonyloxyimino) -2-phenylacetonitrile (Boc-ON) method
  • c) Preparation of Boc-Arg (Mts) -OH
  • i) preparation of N-Carbobenzyloxy L-Arg
  • ii) Preparation of 2-Arg (Mts) -OH
  • iii) Removal of Benzyloxycarbonyl (Z) group: Preparation of Boc-Arg (Mts) -OH
  • 6. Analysis of protected amino acids
  • 7. Estimation of halogen content in functionalized tetraethyleneglycol diacrylate (TTEGDA) -cross linked polystyrene resins
  • 8. Attachment of first amino acid to the resin
  • 9. Estimation of amino group by picric acid method
  • 10. General procedure for solid phase synthesis of peptides
  • 11. General procedure for photolytic cleavage
  • 12. Column chromatography
  • 13. Thin layer chromatography
  • i) Ninhydrin
  • ii) Chlorine-Starch-Potassium Iodide Reagent (Rydons Reagent)
  • iii) Iodine
  • iv) Sakaguchi Reagent
  • 14. Amino acid analysis
  • 15. Preparation of Polymeric supports
  • i) Solution copolynerisation of styrene and tetraethyleneglycol diacrylate
  • ii) Preparation of tetraethyleneglycol diacrylate crosslinked polystyrene supports suspension polynerisation
  • 16. Functionalization of Tetraethyleneglycol Diacrylate-Crosslinked polystyrene support
  • i) Chloromethylation of tetraethyleneglycol diacrylate-crosslinked polystyrene support
  • ii) Preparation -of aminomethyl tetraethyleneglycol diacrylate-crosslinked polystyrene resin
  • iii) Preparation -of 4-chloromethyl-3-nitrotetraethyleneglycol diacrylate polystyrene
  • iv) Preparation -of α -bromopropionyl tetraethylene glycol diacrylate-crosslinked polystyrene resin
  • v) Preparation of α- minopropionyl resin& -aminopropionyl resin
  • vi) Preparation -of 4-bromonethyl benzoic acid
  • vii) Preparation -of 4-bromomethyl-3-nitrobenzoic acid
  • viii) Preparation -of 4-bromonethyl-3-nitrobenzanidomethyl tetraethyleneglycol diacrylate crosslinked polystyrene resin
  • ix) Preparation of 4-aminomethyl-3-nitrobenzamidomethyl tetraethyleneglycol diacrylate polystyrene resin
  • X) Preparation -of 4-hydroxynethyl phenoxymethyl tetraethyleneglycol diacrylate-crosslinked polystyrene resin (l0)
  • 17. Solvent imbibition measurements of TTEGDA-cross linked polystyrene resin
  • 18. Stability studies of TTEGDA crosslinked polystyrene resin
  • 19. Synthesis of protected peptides using 4-chloromethyl-3-nitro TTEGDA cross linked polystyrene support
  • i Synthesis -of Boc-Met-Leu-Ala-OMe
  • ii) Prepara-ion of Boc-Ala-Val-Gly-OEt
  • iii) Preparation -of Boc-Met-Leu-Phe-OMe
  • iv) Synthesis -of Boc-Val-Gly-OEt
  • v) Synthesis of Boc-Val-Gly-OEt -DCC coupling of Boc-Val and Gly-OEt
  • vi) Preparation of Boc-Phe-Gly-OEt
  • 20. Synthesis of Boc (Ala-Leu-Ala) 4OMe peptide on high-capacity chloromethyl TTEGDA-cross linked polystyrene resin
  • i) Cleavage of Boc (Ala-Leu-Ala) OMe from the Solid Support by Trans-esterification
  • 21. Synthesis of model peptides on 4-bromomethyl-3-nitrobenzamidomethyl TTEGDA-cross linked polystyrene support
  • i) Esterification of Boc-Leu with Bromomethyl resin
  • ii) Solid Phase synthesis of Boc-Leu-Leu-Leu-Leu
  • iii) Solid Phase Synthesis of Boc-Gly-Val-Ala-Leu
  • 22. Synthesis of Boc-Val-Glu (OBzl) -Ala Leu-Tyr (Bzl) -Leu-NH2 on 4-amino methyl-3-nitrobenzamidomethyl TTEGDA cross linked polystyrene resin
  • 23. Solid phase synthesis of Boc-Met Phe-Leu-OH using A-bromopropionyl TTEGDA-cross linked polystyrene support
  • 24. Synthesis of Boc-Leu-Ala-Gly-Val-NH2 and Boc-Phe-Phe-Gly-Leu-NH2 using α -aminopropionyl TTEGDA-cross linked polystyrene resin
  • 1) BOC-Phe-Phe-Gly-Leu-Met-NH2
  • 25. Synthesis of biologically important peptides using chloromethyl TTEGDA crosslinked polystyrene resin
  • i) Synthesis of Deltorphin: Tyr-D-Ala-Phe-Asp-Val-Val-Gly-NH2
  • ii) Synthesis of cytoadhesive inhibitory peptide: Gly-Arq-Gly-Asp-Ser-Pro
  • iii) Cleavage of Gly-Arg-Gly-Asp-Ser-Pro from the peptide resin (22) using trifluoroacetic acid
  • iv) Synthesis -of Gly-Arg-Gly-Glu-Ser-Pro
  • v) Synthesis of nuclear signal sequence Ser-Thr-Pro-Pro-Lys-Lys-Lys-Arg-Lys-Val-Cys (Acm)
  • 26. Synthesis of pardaxin sequences 16-33, 5-33 and 1-33
  • i Cleavage of 16-33 pardaxin pepkide from the resin- (22) using trifluoroacetic acid
  • ii) Cleavage of the 5-33 pardaxin from the resin (23) using trifluoroacetic acid
  • iii) Cleavage of the 33-residue pardaxin peptide-toxin from the resin (24) usinq trifluoroacetic acid
  • 27. Manual microsequencing of (5-33) and (1-33) pardaxin
  • 1. Set-up
  • 2. Coupling
  • 3. Washing
  • 4. Extraction
  • 5. Conversion
  • 28. Synthesis of pardaxin (1-26) hydrophobic segment on high capacity chloromethyl TTEGDA crosslinked polystyrene resin
  • i) Cleavage of 1-26 pardaxin segment from the resin (25) using trifluoroacetic acid
  • ii) Purification of 1-26 pardaxin peptide
  • iii) Automatic Edman degradation of 1-26 seqment of pardaxin sequence
  • IV. TETRAEHYLENEGLYCOL DIACRYLATE (TTEGDA) CROSSLINKED POLYSTYRENE: A NEW POLYMERIC SUPPORT FOR PEPTIDE SYNTHESIS
  • Results and Discussion
  • 1. Polymer synthesis
  • 2. Functionalization of tetra ethylene glycol diacrylate (TTEGDA) -cross linked polystyrene resin
  • Fig.IV.1 Scanning Electron Micrograph of TTEGDA Crosslinked Polystyrene Beads
  • 3. Preparation of chloromethyl resin
  • 4. Preparation of 4-chloromethyl-3 nitro TTEGDA-cross linked polystyrene resin
  • 5. Introduction of amino methyl groups in TTEGDA-cross linked polystyrene resin
  • 6. Preparation of α-bromopropionyl and α-aminopropionyl TTEGDA-cross linked polystyrene resin
  • 7. Preparation of 4-bromomethyl-3nitrobenzamidomethyl and 4-aminomethyl-3-nitrobenzamidomethyl TTEGDA-cross linked polystyrene
  • 8. Preparation of 4- (hydroxymethyl) phenoxymethyl TTEGDA-cross linked polystyrene
  • 9. Characterization of TTEGDA-cross linked polystyrene
  • 10. Swelling, salvation and stability of TTEGDA-cross linked polystyrene
  • V. PEPTIDE SYNTHESIS USING TETRAETHYLENEGLYCOL DIACRYLATE (TTEGDA) -CROSS LINKED POLYSTYRENE SUPPORTS
  • Results and Discussion
  • 1. Synthesis of protected model peptides on 4-chloromethyl-3-nitro TTEGDA-cross linked polystyrene
  • 2. Mechanism of photolysis
  • 3. Synthesis of Boc (Ala-Leu-Ala) 4-OMe on a high capacity chloromethyl TTEGDA-cross linked polystyrene
  • Fig.v.1.a) Scanning Electron Micrographs of TTEGDA crosslinked polymer Beads
  • Fig.v.1.b) A Single Bead Enlarged from Fig.v.1.a
  • 4. Synthesis of protected peptide segments on photosensitive 4-bromomethyl-3-nitrobenzamidomethyl TTEGDA-cross linked polystyrene
  • i) Synthesis of Boc -Leu-Leu-Leu-Leu
  • ii) Synthesis of Boc-Gly-Val-Ala-Leu
  • 5. Synthesis of peptide amides on 4-aminomethyl-3-nitrobenzamidomethyI TTEGDA-cross linked polystyrene
  • 6. Synthesis of Boc-Met-Phe-Leu using α-bromopropionyl TTEGDA-cross linked polystyrene
  • 7. Synthesis of peptide amides using α-aminopropionyl TTEGDA-cross linked polystyrene
  • 8. Synthesis of substance P (7-11) segment on α -aminopropionyl TTEGDA crosslinked polystyrene
  • 9. Synthesis of opioid agonist deltorphin on high capacity chloromethyl TTEGDA-cross linked polystyrene
  • 10. Synthesis of cytoadhesive inhibitory peptides Gly-Arg-Gly-Asp / Glu-Ser-Pro on high capacity chloromethyl TTEGDA-cross linked polystyrene
  • 11. Synthesis of nuclear signal sequence on chloromethyl TTEGDA crosslinked polystyrene
  • 12. Synthesis of pardaxin, a 33-residue peptide toxin, on high capacity TTEGDA-cross linked polystyrene
  • 13. Synthesis of pardaxin sequence (16-33), (5-33) and (1-33)
  • 14. Synthesis of 26-residue peptide corresponding to the N-terminal hydrophobic region of pardaxin on high capacity TTEGDA-cross linked polystyrene
  • VI. SUMMARY AND OUTLOOK
  • VII REFERENCES