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- Publisher Website: 10.1002/cbic.202100144
- Scopus: eid_2-s2.0-85105414069
- PMID: 33891355
- WOS: WOS:000647964700001
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Article: Recent Advances on the Selection Methods of DNA‐Encoded Libraries
Title | Recent Advances on the Selection Methods of DNA‐Encoded Libraries |
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Authors | |
Keywords | Combinatorial library DNA-encoded library Drug discovery High throughput screening Ligand discovery |
Issue Date | 2021 |
Publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.chembiochem.com |
Citation | ChemBioChem, 2021, v. 22 n. 14, p. 2384-2397 How to Cite? |
Abstract | DNA-encoded libraries (DEL) have come of age and become a major technology platform for ligand discovery in both academia and the pharmaceutical industry. Technological maturation in the past two decades and the recent explosive developments of DEL-compatible chemistries have greatly improved the chemical diversity of DELs and fueled its applications in drug discovery. A relatively less-covered aspect of DELs is the selection method. Typically, DEL selection is considered as a binding assay and the selection is conducted with purified protein targets immobilized on a matrix, and the binders are separated from the non-binding background via physical washes. However, the recent innovations in DEL selection methods have not only expanded the target scope of DELs, but also revealed the potential of the DEL technology as a powerful tool in exploring fundamental biology. In this Review, we first cover the 'classic' DEL selection methods with purified proteins on solid phase, and then we discuss the strategies to realize DEL selections in solution phase. Finally, we focus on the emerging approaches for DELs to interrogate complex biological targets. |
Persistent Identifier | http://hdl.handle.net/10722/301511 |
ISSN | 2023 Impact Factor: 2.6 2023 SCImago Journal Rankings: 0.809 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Huang, Y | - |
dc.contributor.author | Li, X | - |
dc.date.accessioned | 2021-08-09T03:40:07Z | - |
dc.date.available | 2021-08-09T03:40:07Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | ChemBioChem, 2021, v. 22 n. 14, p. 2384-2397 | - |
dc.identifier.issn | 1439-4227 | - |
dc.identifier.uri | http://hdl.handle.net/10722/301511 | - |
dc.description.abstract | DNA-encoded libraries (DEL) have come of age and become a major technology platform for ligand discovery in both academia and the pharmaceutical industry. Technological maturation in the past two decades and the recent explosive developments of DEL-compatible chemistries have greatly improved the chemical diversity of DELs and fueled its applications in drug discovery. A relatively less-covered aspect of DELs is the selection method. Typically, DEL selection is considered as a binding assay and the selection is conducted with purified protein targets immobilized on a matrix, and the binders are separated from the non-binding background via physical washes. However, the recent innovations in DEL selection methods have not only expanded the target scope of DELs, but also revealed the potential of the DEL technology as a powerful tool in exploring fundamental biology. In this Review, we first cover the 'classic' DEL selection methods with purified proteins on solid phase, and then we discuss the strategies to realize DEL selections in solution phase. Finally, we focus on the emerging approaches for DELs to interrogate complex biological targets. | - |
dc.language | eng | - |
dc.publisher | Wiley - V C H Verlag GmbH & Co KGaA. The Journal's web site is located at http://www.chembiochem.com | - |
dc.relation.ispartof | ChemBioChem | - |
dc.rights | Submitted (preprint) Version This is the pre-peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. Accepted (peer-reviewed) Version This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions. | - |
dc.subject | Combinatorial library | - |
dc.subject | DNA-encoded library | - |
dc.subject | Drug discovery | - |
dc.subject | High throughput screening | - |
dc.subject | Ligand discovery | - |
dc.title | Recent Advances on the Selection Methods of DNA‐Encoded Libraries | - |
dc.type | Article | - |
dc.identifier.email | Huang, Y: huangyr0@hku.hk | - |
dc.identifier.email | Li, X: xiaoyuli@hku.hk | - |
dc.identifier.authority | Li, X=rp02080 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/cbic.202100144 | - |
dc.identifier.pmid | 33891355 | - |
dc.identifier.scopus | eid_2-s2.0-85105414069 | - |
dc.identifier.hkuros | 324090 | - |
dc.identifier.volume | 22 | - |
dc.identifier.issue | 14 | - |
dc.identifier.spage | 2384 | - |
dc.identifier.epage | 2397 | - |
dc.identifier.isi | WOS:000647964700001 | - |
dc.publisher.place | Germany | - |