[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

Pinilla et al., 1993 - Google Patents

Synthetic peptide combinatorial libraries (SPCLs): identification of the antigenic determinant of β-endorphin recognized by monoclonal antibody 3E7

Pinilla et al., 1993

Document ID
405086894359365268
Author
Pinilla C
Appel J
Houghten R
Publication year
Publication venue
Gene

External Links

Snippet

The use of synthetic peptide combinatorial libraries (SPCLs), each composed of tens of millions of peptides, is described here for the identification of bioactive peptides. The identification of optimal peptide sequences is achieved through the screening of SPCLs in …
Continue reading at www.sciencedirect.com (other versions)

Classifications

    • 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
    • C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
    • C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
    • 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
    • C07K1/04—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
    • 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
    • C07K1/06—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
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/10—Tetrapeptides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides

Similar Documents

Publication Publication Date Title
Pinilla et al. Synthetic peptide combinatorial libraries (SPCLs): identification of the antigenic determinant of β-endorphin recognized by monoclonal antibody 3E7
Owens et al. The rapid identification of HIV protease inhibitors through the synthesis and screening of defined peptide mixtures
Dooley et al. Acetalins: opioid receptor antagonists determined through the use of synthetic peptide combinatorial libraries.
US5734018A (en) Peptide mixtures
US5010175A (en) General method for producing and selecting peptides with specific properties
Ostresh et al. Peptide libraries: determination of relative reaction rates of protected amino acids in competitive couplings
Pinilla et al. A review of the utility of soluble peptide combinatorial libraries
Dooley et al. The use of positional scanning synthetic peptide combinatorial libraries for the rapid determination of opioid receptor ligands
Hansen et al. Fmoc solid-phase peptide synthesis
Jung et al. Multiple peptide synthesis methods and their applications. New synthetic methods (87)
US5556762A (en) Scanning synthetic peptide combinatorial libraries: oligopeptide mixture sets having a one predetermined residue at a single, predetermined position, methods of making and using the same
EP0722458B1 (en) Peralkylated oligopeptide mixtures
AU719469B2 (en) Conformationally-restricted combinatorial library composition and method
Houghten et al. The use of synthetic peptide combinatorial libraries for the determination of peptide ligands in radio-receptor assays: opioid peptides
EP0639584A1 (en) Preparation and screening of highly diverse peptide libraries for binding activity
US6287787B1 (en) Dimeric oligopeptide mixture sets
Wang et al. Applications of topologically segregated bilayer beads in ‘one‐bead one‐compound’combinatorial libraries
US5225533A (en) General method for producing and selecting peptides with specific properties
Choi et al. Comparison of methods for the Fmoc solid‐phase synthesis and cleavage of a peptide containing both tryptophan and arginine
Liu et al. Automatic Edman microsequencing of peptides containing multiple unnatural amino acids
Xue et al. A covalently constrained congener of the Saccharomyces cerevisiae tridecapeptide mating pheromone is an agonist
JPH0753588A (en) Automatic protection of deallylation in solid-phase synthesis
Herman et al. Optimization of the synthesis of peptide combinatorial libraries using a one-pot method
Moore et al. Peptide design considerations
WO1996006353A1 (en) Lysine/leucine polypeptides, mixture sets and libraries thereof