Kassem et al., 2009 - Google Patents
To rink or not to rink amide link, that is the question to address for more economical and environmentally sound solid-phase peptide synthesisKassem et al., 2009
View PDF- Document ID
- 13713558252918526857
- Author
- Kassem T
- Sabatino D
- Jia X
- Zhu X
- Lubell W
- Publication year
- Publication venue
- International Journal of Peptide Research and Therapeutics
External Links
Snippet
A comparative study is presented on the solid-phase peptide synthesis (SPPS) of the acyl carrier protein (ACP 65–74) sequence on a series of Rink amide resins possessing different matrix structures: poly (vinyl alcohol)-graft-poly (ethylene glycol)(PVA-g-PEG, 4), Tentagel-S …
- 150000001408 amides 0 title abstract description 21
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
- C07K1/047—Simultaneous synthesis of different peptide species; Peptide libraries
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/04—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers
- C07K1/042—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length on carriers characterised by the nature of the carrier
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/06—Linear peptides containing only normal peptide links having 5 to 11 amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/107—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides
- C07K1/1072—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by chemical modification of precursor peptides by covalent attachment of residues or functional groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/08—Linear peptides containing only normal peptide links having 12 to 20 amino acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/14—Extraction; Separation; Purification
- C07K1/16—Extraction; Separation; Purification by chromatography
- C07K1/22—Affinity chromatography or related techniques based upon selective absorption processes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/06—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
- C07K1/061—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
- C07K1/003—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by transforming the C-terminal amino acid to amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1034—Isolating an individual clone by screening libraries
- C12N15/1037—Screening libraries presented on the surface of microorganisms, e.g. phage display, E. coli display
-
- C—CHEMISTRY; METALLURGY
- C40—COMBINATORIAL CHEMISTRY
- C40B—COMBINATORIAL CHEMISTRY; LIBRARIES, e.g. CHEMICAL LIBRARIES, IN SILICO LIBRARIES
- C40B40/00—Libraries per se, e.g. arrays, mixtures
- C40B40/04—Libraries containing only organic compounds
- C40B40/10—Libraries containing peptides or polypeptides, or derivatives thereof
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Adams et al. | A Reinvestigation of the Preparation, Properties, and Applications of Aminomethyl and 4-Methylbenzhydrylamine Polystyrene Resins1 | |
Tam et al. | Coupling difficulty associated with interchain clustering and phase transition in solid phase peptide synthesis | |
JP3394777B2 (en) | Topologically separated, encoded solid-phase library | |
JPH04501709A (en) | Peptide synthesis methods and use of solid supports in the methods | |
JPH10500951A (en) | Coded combinatorial library | |
Darlak et al. | Facile preparation of disulfide‐bridged peptides using the polymer‐supported oxidant CLEAR‐OXTM | |
KR102243870B1 (en) | Cyclic peptides, affinity chromatography carriers, labeled antibodies, antibody drug complexes, and pharmaceutical preparations | |
Kassem et al. | To rink or not to rink amide link, that is the question to address for more economical and environmentally sound solid-phase peptide synthesis | |
Huang et al. | Enhanced native chemical ligation by peptide conjugation in trifluoroacetic acid | |
Xu et al. | A novel approach to chemical microarray using ketone-modified macromolecular scaffolds: application in micro cell-adhesion assay | |
Moss | Guide for resin and linker selection in solid‐phase peptide synthesis | |
Avital-Shmilovici et al. | Mega-High-Throughput Screening Platform for the Discovery of Biologically Relevant Sequence-Defined Non-Natural Polymers | |
Leena et al. | Syntheses, characterization and application of cross‐linked polystyrene− ethyleneglycol acrylate resin (CLPSER) as a novel polymer support for polypeptide syntheses | |
Cho et al. | Controllable Core–Shell-Type Resin for Solid-Phase Peptide Synthesis | |
Roice et al. | Optimization in peptide synthetic conditions of 1, 4-butanediol dimethacrylate cross-linked polystyrene resin and its efficiency in solid phase peptide synthesis | |
Gauthier et al. | Peptide Synthesis: Methods and Protocols | |
Selvam et al. | Synthesis of biologically active hydrophobic peptide by using novel polymer support: improved Fmoc solid phase methodology | |
Siyad et al. | Solid-Phase Peptide Synthesis of Endothelin Receptor Antagonists on Novel Flexible, Styrene− Acryloyloxyhydroxypropyl Methacrylate− Tripropyleneglycol Diacrylate [SAT] Resin | |
CA2254987A1 (en) | Acyl transfer with stabilised transition complex using catalyst with catalytic imidazole (e.g. histidine) function | |
KR101978446B1 (en) | Ethylene glycol derivatives for solid phase application and core-shell type graft support | |
Siyad et al. | Synthesis, characterization, and evaluation of PS‐PPDC resin: A novel flexible cross‐linked polymeric support for solid‐phase organic synthesis | |
Kim et al. | Preparation of tri (ethylene glycol) grafted core‐shell type polymer support for solid‐phase peptide synthesis | |
KR101664338B1 (en) | Novel peptides with specific binding to Fc domain of Immunoglobulin G | |
Siyad et al. | Synthesis and characterization of linear and cyclic endothelin peptides on PEGylated poly (O-benzyl ether) dendrimeric supports | |
Roice et al. | SYNTHESIS OF ALZHEIMER'S 0-AMYLOID PEPTIDE FRAGMENT (33-42) ON A NEW CHEMICALLY INERT PS-BDODMA SUPPORT |