Book Chapter10.1007/978-1-59259-642-3_42
Solid-Phase Peptide Synthesis
98
TL;DR: Using Edman Sequencing as Tool for Characterization of Synthetic Peptides and Proteins and Analysis of Peptide Synthesis Products by Electrospary Ionization Mass Spectrometry, J.H. Fields and G.B. Fields, Construction of Active Protein Molecular Architecture Using Self-Assembling Peptid-Amphiphiles.
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Abstract: B. Merrifield, Concept and Early Development of Solid-Phase Peptide Synthesis. Methods for Solid-Phase Assembly of Peptides: P.F. Alewood, D. Alewood, L. Miranda, S. Love, W. Meutermans, and D. Wilson, Rapid in Situ Neutralization Protocols for Boc and Fmoc Solid-Phase Chemistries. J.M. Stewart, Cleavage Methods Following Boc-Based Solid-Phase Peptide Synthesis. D.A. Wellings and E. Atherton, Standard Fmoc Protocols. C.G. Fields and G.B. Fields, Trifluoroacetic Acid Cleavage and Deprotection of Resin-Bound Peptides Following Synthesis by Fmoc Chemistry. M. Meldal, Properties of Solid Supports. F. Albericio and L.A. Carpino, Coupling Reagents and Activation. M.F. Songster and G. Barany, Handles in Solid-Phase Peptide Synthesis. C. Blackburn and S.A. Kates, Solid-Phase Synthesis of Cyclic Homodetic Peptides. I. Annis, B. Hargittai, and G. Barany, Disulfide Bond Formation in Peptides. J. Kihlberg, M. Elofsson, and L.A. Salvador, Direct Synthesis of Glycosylated Amino Acids from Carbohydrate Peracetates and Fmoc Amino Acids: Solid-Phase Synthesis of Biomedicinally Interesting Glycopeptides. J.W. Perich, Synthesis of Phosphopeptides Using Modern Chemical Approaches. S.B.H. Kent, Chemoselective Ligation. A.C. Braisted, J.K. Judice, and J.A. Wells, Synthesis of Proteins by Subtiligase. F. Albericio, P. Lloyd-Williams, and E. Giralt, Convergent Solid-Phase Synthesis. M. Lebl and V.Krchnak, Peptide Libraries. Analytical Techniques: G.A. Grant, M.W. Crankshaw, and J. Gorka, Edman Sequencing as Tool for Characterization of Synthetic Peptides. A.J. Smith, Amino Acid Analysis. C.T. Mant, L.H. Kondejewski, P.J. Cachia, O.D. Monera, and R.S. Hodges, Analysis of Synthetic Peptides by High-performance Liquid Chromatography. A. Sanchez and A.J. Smith, Capillary Electrophoresis. S. Beranova-Giorgianni and D.M. Desiderio, Fast Atom Bombardment Mass Spectrometry of Synthetic Peptides. D.J. Burdick and J.T. Stults, Analysis of Peptide Synthesis Products by Electrospary Ionization Mass Spectrometry. W.T. Moore, Laser Desorption. Specialized Applications: T.W. Muir, P.E. Dawson, M.C. Fitzgerald, and S.B.H. Kent, Protein Signature Analysis for Studying Structure-Activity Relationships in Peptides and Proteins. J.L. Lauer and G.B. Fields, In Vitro Incorporation of Synthetic Peptides into Cells. Y-C. Yu, T. Pakalns, Y.Dori, J.B. McCarthy, M. Tirrell, and G.B. Fields, Construction of Biologically Active Protein Molecular Architecture Using Self-Assembling Peptide-Amphiphiles. E. Barbar, C. Woodward, and G. Barany, Nuclear Magnetic Resonance Characterization of Synthetically Derived Partially Folded Proteins. J.P. Tam and J.C. Spetzler, Multiple Antigen Peptide System. J.D. Wade and G.W. Tregear, Relaxin. K.H. Mayo, Solution Nuclear Magnetic Resonance Characterization of Peptide Folding. T.A. Cross, Solid-State NMR Characterization of the Gramicidin Channel Structure. R.H. Angeletti, L.F. Bonewald, G.B. Fields, Six-Year Study of Peptide Synthesis. Index.
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Advances in Fmoc solid‐phase peptide synthesis
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Structure of the transmembrane region of the M2 protein H(+) channel.
TL;DR: A high‐resolution structure of the monomer backbone and a detailed description of its orientation with respect to the bilayer were achieved using orientational restraints from solid‐state NMR, revealing the tetrameric structure of this H+ channel is constrained substantially.
Helix tilt of the M2 transmembrane peptide from influenza A virus: an intrinsic property.
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References
Synthesis of proteins by native chemical ligation
TL;DR: The technique of native chemical ligation is employable for chemically synthesizing full length proteins as discussed by the authors, which are chemically identical to proteins produced by cell free synthesis, and can be refolded and/or oxidized to form native disulfide-containing protein molecules.
3.3K
Solid phase peptide synthesis utilizing 9‐fluorenylmethoxycarbonyl amino acids
Gregg B. Fields,Richard L. Noble +1 more
TL;DR: The great variety of conditions under which Fmoc solid phase peptide synthesis may be carried out represents a truly "orthogonal" scheme, and thus offers many unique opportunities for bioorganic chemistry.
2.5K
Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1‐Hydroxy‐benzotriazolen
Wolfgang König,Rolf Geiger +1 more
TL;DR: In this article, the authors show that 1-Hydroxy-benzotriazol and 1-hydroxy-acetyl carbodiimid-methode eignen sich als Zusatze bei der Dicyclohexylcarbodiimids-Methode zur Synthese von Peptiden, verhindern die N-Acyl-harnstoffbildung and fuhren in hoher Ausbeute.
1.5K
Solid phase synthesis
TL;DR: The purpose today is to describe the chemical synthesis of peptides and proteins and to discuss the use of the synthetic approach to answer various biological questions.
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