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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

Exploration of the HIF-1α/p300 interface using peptide and Adhiron phage display technologies

TL;DR: A detailed biophysical analysis of the native interaction of the HIF-1α/p300 protein-protein interaction with both peptide and Adhiron phage display experiments is reported to identify novel binding motifs and binding regions of the surface of p300 to inform future inhibitor design.
Journal ArticleDOI

In situ click chemistry: from small molecule discovery to synthetic antibodies

TL;DR: This review presents a review of Iterative Peptide In Situ Click Chemistry (IPISC), a novel screening technology for designing peptide multiligands with high affinity and specificity, and discusses the recent progress in ligand design through IPISC and related approaches.
Patent

A structured peptide scaffold for displaying turn libraries on phage

TL;DR: In this paper, a model system for structure-activity analysis of peptide or protein molecules involved in important biological processes is presented, which are combinatorial peptide libraries comprising disulfide-constrained cyclic peptides.
Patent

Inhibition of stat3 signal transduction for human cancer therapy

TL;DR: Signal Transducer and Activator of Transcription (STAT) proteins have a fundamental role cell signaling, and are activated by a large number of cytokines and growth factors as discussed by the authors.
Journal ArticleDOI

Tumour suppressor genes and molecular chaperones

TL;DR: The p53 protein interacts with members of the hsp70 chaperone family which it is shown can regulate its function, leading to an attractive model of p53 as an essential checkpoint control.
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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