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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

New molecular biology methods for protein engineering

TL;DR: This review outlines recent advances in the application of molecular biological techniques to the study of protein structure and function through methods for oligonucleotide-directed mutagenesis; mutational strategies for identifying functional residues and domains; systems for expression; and future developments.
Journal ArticleDOI

An in vitro selection strategy for conferring protease resistance to ligand binding peptides

TL;DR: In vitro display technology, CIS display, is used to enhance the proteolytic resistance of ligand-binding peptides by selection of protecting motifs from a large peptide library, which translated into increased resistance to plasma proteases in vitro and to an increase in circulating half-lives in rats.
Journal ArticleDOI

Identification of Soft Matter Binding Peptide Ligands Using Phage Display.

TL;DR: The article will provide an overview of the different peptide ligands that have been identified by phage display that bind to these "soft matter" targets and the different characterization techniques that allow the determination of the affinity of the identified ligands to the respective substrates.
Journal ArticleDOI

Ligand discovery using small molecule microarrays.

TL;DR: In this review, some of the technical issues related to the manufacture and screening of small molecule microarrays, as well as prospects for small moleculemicroarrays in several areas of drug discovery and chemistry, are discussed.
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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