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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

Interaction and co-encapsidation of human immunodeficiency virus type 1 Gag and Vif recombinant proteins

TL;DR: The data suggest a direct intracellular Gag-Vif interaction and the occurrence of a Pr55Gag-mediated membrane-targeting pathway for Vif in Sf9 cells.
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Peptides targeting caspase inhibitors.

TL;DR: It is demonstrated that an internalizing version of the XIAP-binding peptide identified in the authors' screenings (PFKQ) can induce programmed cell death in leukemia cells.
Patent

Method of selection of proteolytic cleavage sites by directed evolution and phagemid display

TL;DR: In this article, a method for identifying and selecting novel substrates for enzymes is provided, which comprises constructing a gene fusion comprising DNA encoding a polypeptide fused to DNA encoding at least a portion of a phage coat protein.
Journal ArticleDOI

Designing scaffolds of peptides for phage display libraries.

TL;DR: It is found that the conformational design of peptides in library is important for selecting high-affinity ligands that bind to every target from a phage peptide library.
Journal ArticleDOI

Identification of epitopes within beta lactoglobulin recognised by polyclonal antibodies using phage display and PEPSCAN

TL;DR: This study has permitted detailed mapping of the major linear antigenic regions within BLG recognised by IgG antibodies from immunised rabbits and mice.
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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