scispace - formally typeset
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
Reads0
Chats0
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.

read more

Citations
More filters
Patent

Molecule that homologizes genotype and phenotype and utilization thereof

TL;DR: In this paper, a method of constructing a molecule that homologizes a genotype and a phenotype is presented, which comprises the steps of (a) preparing a DNA containing a gene free from termination codon, (b) transcribing the DNA into a RNA, (c) joining a spacer comprising a DNA-RNA chimera to the 3' end of the RNA, and (d) further joining to the product of ligation a nucleoside or a substance having a chemical structure analogous to that of the n-oside, the noside and
Journal ArticleDOI

Cyclic Peptides: Promising Scaffolds for Biopharmaceuticals

TL;DR: Recent progress in methodologies for peptide cyclization and screening and use of bioactive cyclic peptides in various applications are discussed.
Patent

Methods for selective targeting

TL;DR: In this article, a selective targeting method is proposed, which comprises contacting a peptide library with an anti-target to allow the peptides to bind; separating non-binding peptides from the anti target bound peptides; and identifying the target-bound peptides.
Journal ArticleDOI

Applications and strategies in nanodiagnosis and nanotherapy in lung cancer

TL;DR: A synopsis of current progress in theranostic applications for lung cancer diagnosis and therapy using NPs including liposome, polymeric NPs, quantum dots, gold NPS, dendrimers, carbon nanotubes and magnetic NPs is provided.
Journal ArticleDOI

Time-course gait analysis of hemiparkinsonian rats following 6-hydroxydopamine lesion

TL;DR: Time-course gait analysis of a unilateral 6-OHDA rodent model provides insight into the compensatory changes of motor functions during the 6-week development of a nigrostriatal lesion, which might be useful for future objective assessment of novel treatments for human PD subjects.
References
More filters
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.
Related Papers (5)