Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Although peptides are well recognised biological molecules in vivo, their selection from libraries is challenging because of relative low affinity whilst in linear conformation. We hypothesized that multiplexed peptides and DNA on the surface of beads would provide a platform for enhanced avidity and the selection of relevant peptides from a library (ORBIT bead display). Using human immunodeficiency virus (HIV-1) gp120 as a target, we identify peptides that inhibit HIV-1 replication in vitro through blocking of protein:protein interaction with the co-receptor CCR5. The bead display approach has many potential applications for probing biological systems and for drug lead development.

Original publication

DOI

10.1038/srep03030

Type

Journal article

Journal

Scientific reports

Publication Date

10/2013

Volume

3

Addresses

1] MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, NIHR Biomedical Research Centre, University of Oxford, UK [2].

Keywords

Humans, HIV-1, Peptides, Peptide Library, beta 2-Microglobulin, Receptors, CCR5, Receptors, HIV, HIV Envelope Protein gp120, Anti-HIV Agents, Microbial Sensitivity Tests, Reproducibility of Results, Microspheres, Protein Binding, Kinetics, High-Throughput Screening Assays