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Journal ArticleDOI

Searching for Peptide Ligands With an Epitope Library

Jamie K. Scott, +1 more
- 27 Jul 1990 - 
- Vol. 249, Iss: 4967, pp 386-390
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TLDR
Tens of millions of short peptides can be easily surveyed for tight binding to an antibody, receptor or other binding protein using an "epitope library".
Abstract
Tens of millions of short peptides can be easily surveyed for tight binding to an antibody, receptor or other binding protein using an "epitope library." The library is a vast mixture of filamentous phage clones, each displaying one peptide sequence on the virion surface. The survey is accomplished by using the binding protein to affinity-purify phage that display tight-binding peptides and propagating the purified phage in Escherichia coli. The amino acid sequences of the peptides displayed on the phage are then determined by sequencing the corresponding coding region in the viral DNA's. Potential applications of the epitope library include investigation of the specificity of antibodies and discovery of mimetic drug candidates.

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Citations
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Journal ArticleDOI

Recent insights into the genotype-phenotype relationship from massively parallel genetic assays.

TL;DR: The technological basis of and recent developments in massively parallel genetics, along with the trends it is uncovering in the genotype–phenotype relationship (distribution of mutation effects, epistasis), their possible mechanistic bases and future directions for advancing towards the goal of predictive genetics are discussed.
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Monoclonal antibodies that recognise filamentous phage: tools for phage display technology.

TL;DR: Six hybridoma cell lines that secrete monoclonal antibodies which specifically bind filamentous phage coat proteins are generated, which are valuable tools to study phage assembly and structure and how these mAb can be exploited in the construction and screening of peptide libraries displayed by the filamentous phase major coat protein.
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Next-generation protein drugs.

TL;DR: Ankyrin repeats generate high-affinity protein binders with biophysical properties that may favor therapeutic applications and be a source of inspiration for new drug candidates.
Patent

Stabilized liquid anti-rsv antibody formulations

TL;DR: In this paper, the authors provide liquid formulations of SYNAGIS or an antigen-binding fragment thereof that immunospecifically bind to a respiratory syncytial virus (RSV) antigen.
Journal ArticleDOI

Preparation of peptides which mimic glycosphingolipids by using phage peptide library and their modulation on β‐galactosidase activity

TL;DR: This is the first report of carbohydrate mimicking peptides which modulate glycosidase activity and binding activity of the peptides to the monoclonal antibodies or Ricinus communis lectin showed that 9‐mer peptides are enough to mimic the epitope carbohydrate structure.
References
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Book

Molecular Cloning: A Laboratory Manual

TL;DR: Molecular Cloning has served as the foundation of technical expertise in labs worldwide for 30 years as mentioned in this paper and has been so popular, or so influential, that no other manual has been more widely used and influential.
Journal ArticleDOI

DNA sequencing with chain-terminating inhibitors

TL;DR: A new method for determining nucleotide sequences in DNA is described, which makes use of the 2',3'-dideoxy and arabinon nucleoside analogues of the normal deoxynucleoside triphosphates, which act as specific chain-terminating inhibitors of DNA polymerase.
Journal ArticleDOI

Rapid and efficient site-specific mutagenesis without phenotypic selection.

TL;DR: The high efficiency, approximately equal to 10-fold greater than that observed using current methods without enrichment procedures, is obtained by using a DNA template containing several uracil residues in place of thymine, which is applied to mutations introduced via both oligonucleotides and error-prone polymerization.
Book ChapterDOI

Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction.

TL;DR: A method whereby a nucleic acid sequence can be exponentially amplified in vitro is described in the chapter, and the possibility of utilizing a heat-stable DNA polymerase is explored so as to avoid the need for addition of new enzyme after each cycle of thermal denaturation.
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