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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

Affinity for the cognate monoclonal antibody of synthetic peptides derived from selection by phage display

TL;DR: The affinity of a given peptide strongly depends on its capacity to maintain the antigenically reactive structure it has on the phage, implying that it is impossible to predict whether high- or low-affinity peptides will be obtained from phage display.
Journal Article

Disulfide-constrained peptides that bind to the extracellular portion of the prostate-specific membrane antigen

TL;DR: In this paper, two separate phage display peptide strategies were applied, in parallel, to purified PSMA protein bound to two separate substrates, and the design allowed for stringent cross-selections, where phage populations from one selection condition could be applied to the alternative substrate.
Journal ArticleDOI

Anti-free prostate-specific antigen monoclonal antibody epitopes defined by mimotopes and molecular modeling.

TL;DR: These epitope localizations are in agreement with the ability of both mAbs to inhibit enzymatic activity and ACT fixation, and could bring information for the generation of clinically relevant PSA assays.
Journal ArticleDOI

In Silico Generation of Peptides by Replica Exchange Monte Carlo: Docking-Based Optimization of Maltose-Binding-Protein Ligands

TL;DR: Ex-novo peptides targeting the maltose site of the Maltose Binding Protein, the prototypical system for the study of protein ligand recognition are developed using a Monte Carlo based protocol to computationally evolve a set of octapeptides starting from a polialanine sequence.
Journal ArticleDOI

Epitope mapping of monoclonal antibodies to keratin 19 using keratin fragments, synthetic peptides and phage peptide libraries

TL;DR: A group of monoclonal antibodies reacting with the intermediate filament protein keratin 19 were studied using different approaches to define the structure and localization of their epitopes to generate tools for monitoring processing and folding in keratin intermediate filaments.
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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