نتایج جستجو برای: random peptide library

تعداد نتایج: 553116  

2010
Maliha Zahid Brett E. Phillips Sean M. Albers Nick Giannoukakis Simon C. Watkins Paul D. Robbins

BACKGROUND A peptide able to transduce cardiac tissue specifically, delivering cargoes to the heart, would be of significant therapeutic potential for delivery of small molecules, proteins and nucleic acids. In order to identify peptide(s) able to transduce heart tissue, biopanning was performed in cell culture and in vivo with a M13 phage peptide display library. METHODS AND RESULTS A cardio...

Background: CD90, a membrane-associated glycoprotein is a marker used to identify mesenchymal stem cells (MSCs). Recent studies have introduced CD90, which induces tumorigenic activity, as a cancer stem cell (CSC) marker in various malignancies. Blocking CD90 activity with anti-CD90 monoclonal antibodies enhanced anti-tumor effects. To date, highly specific antibody single-chain variable fragme...

Journal: :Molecular cancer therapeutics 2005
Olulanu H Aina Jan Marik Ruiwu Liu Derick H Lau Kit S Lam

Using "one-bead one-compound" combinatorial chemistry technology, we generated random peptide libraries containing millions of 90 mum TentaGel beads, each with its own unique amino acid sequence. A cyclic random 8-mer library was screened with CAOV-3 (a human ovarian adenocarcinoma cell line) and beads with a unique ligand that bind to the cell surface receptors were coated by one or more layer...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2008
David A C Beck Darwin O V Alonso Daigo Inoyama Valerie Daggett

Here, we compare the distributions of main chain (Phi,Psi) angles (i.e., Ramachandran maps) of the 20 naturally occurring amino acids in three contexts: (i) molecular dynamics (MD) simulations of Gly-Gly-X-Gly-Gly pentapeptides in water at 298 K with exhaustive sampling, where X = the amino acid in question; (ii) 188 independent protein simulations in water at 298 K from our Dynameomics Project...

2013
Andrew J. Creese Jade Smart Helen J. Cooper

Large scale analysis of proteins by mass spectrometry is becoming increasingly routine; however, the presence of peptide isomers remains a significant challenge for both identification and quantitation in proteomics. Classes of isomers include sequence inversions, structural isomers, and localization variants. In many cases, liquid chromatography is inadequate for separation of peptide isomers....

Journal: :Journal of biotechnology 2002
Nina Bandmann James Van Alstine Andres Veide Per-Ake Nygren

Aqueous two-phase systems allow for the unequal distribution of proteins and other molecules in water-rich solutions containing phase separating polymers or surfactants. One approach to improve the partitioning properties of recombinant proteins is to produce the proteins as fused to certain peptide tags. However, the rational design of such tags has proven difficult since it involves a comprom...

Journal: :The Journal of Experimental Medicine 2000
Reinhard Obst Nikolai Netuschil Karsten Klopfer Stefan Stevanović Hans-Georg Rammensee

By analyzing T cell responses against foreign major histocompatibility complex (MHC) molecules loaded with peptide libraries and defined self- and viral peptides, we demonstrate a profound influence of self-MHC molecules on the repertoire of alloreactive T cells: the closer the foreign MHC molecule is related to the T cell's MHC, the higher is the proportion of peptide-specific, alloreactive ("...

Journal: :BMC Pharmacology 2009
Rebecca A Roof David L Roman Samuel T Clements Katarzyna Sobczyk-Kojiro Levi L Blazer Shodai Ota Henry I Mosberg Richard R Neubig

BACKGROUND Regulators of G protein signaling (RGSs) accelerate GTP hydrolysis by Galpha subunits and profoundly inhibit signaling by G protein-coupled receptors (GPCRs). The distinct expression patterns and pathophysiologic regulation of RGS proteins suggest that inhibitors may have therapeutic potential. We recently described a focused one-bead, one-compound (OBOC) library screen to identify p...

2017
Jason M. Goldstein Joo Lee Xiaoling Tang Anne E. Boyer John R. Barr Dennis A. Bagarozzi Conrad P. Quinn

AVR1674 and AVR1675 are monoclonal antibodies (mAbs) that bind with high specificity to anthrax toxin lethal factor (LF) and lethal toxin (LTx). These mAbs have been used as pivotal reagents to develop anthrax toxin detection tests using mass spectrometry. The mAbs were demonstrated to bind LF with good affinity (KD 10−7–10−9 M) and to enhance LF-mediated cleavage of synthetic peptide substrate...

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