An integrated platform approach enables discovery of potent, selective and ligand-competitive cyclic peptides targeting the GIP receptor

Author:

Bhushan Bhaskar1,Granata Daniele2,Kaas Christian S.2,Kasimova Marina A.2,Ren Qiansheng3,Cramer Christian N.2ORCID,White Mark D.1,Hansen Ann Maria K.4,Fledelius Christian4,Invernizzi Gaetano2,Deibler Kristine5,Coleman Oliver D.6,Zhao Xin3,Qu Xinping3,Liu Haimo3,Zurmühl Silvana S.2,Kodra Janos T.2ORCID,Kawamura Akane16ORCID,Münzel Martin2ORCID

Affiliation:

1. Department of Chemistry, Oxford University, Chemistry Research Laboratory, 12 Mansfield Road, Oxford, OX1 3TA, UK

2. Global Research Technologies, Novo Nordisk A/S, Novo Nordisk Park, 2760 Måløv, Denmark

3. Novo Nordisk Research Center China, Novo Nordisk A/S, Shengmingyuan West Ring Rd, Changping District, Beijing, China

4. Global Drug Discovery, Novo Nordisk A/S, Novo Nordisk Park, 2760 Måløv, Denmark

5. Novo Nordisk Research Center Seattle, Novo Nordisk A/S, 530 Fairview Ave N # 5000, Seattle, WA 98109, USA

6. School of Natural and Environmental Sciences, Chemistry, Newcastle University, Bedson Building, Kings Road Newcastle University Newcastle Upon Tyne, NE1 7RU, UK

Abstract

mRNA display generates vast datasets of protein binders. Bioinformatic clustering of the sequences combined with high throughput synthesis and analysis methods allow efficient prioritisation of hits for in vivo experiments.

Funder

Novo Nordisk

H2020 European Research Council

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

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