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- Publisher Website: 10.1002/chem.201802067
- Scopus: eid_2-s2.0-85054558561
- PMID: 29947435
- WOS: WOS:000451901200003
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Article: Advances in Native Chemical Ligation-Desulfurization: A Powerful Strategy for Peptide and Protein Synthesis
Title | Advances in Native Chemical Ligation-Desulfurization: A Powerful Strategy for Peptide and Protein Synthesis |
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Authors | |
Keywords | Cysteine surrogates Desulfurization Native chemical ligation (NCL) One-pot synthesis Proteins |
Issue Date | 2018 |
Publisher | Wiley - VCH Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/chemistry |
Citation | Chemistry - A European Journal, 2018, v. 24 n. 66, p. 17397-17404 How to Cite? |
Abstract | Cysteine‐based native chemical ligation (NCL) has been a very powerful approach for convergent synthesis of peptides and proteins. However, owing to the low abundance of cysteine (Cys) in proteins, applications of NCL in protein chemical synthesis are limited. To expand the peptide ligation toolbox, NCL followed by desulfurization has been developed to enable peptide ligation at Xaa‐Ala conjunctions, that is, formal “alanine ligation”. In this regard, effective peptide desulfurization methods are critical. This Concept article summarizes the development of different desulfurization strategies for peptide and protein chemical synthesis. |
Persistent Identifier | http://hdl.handle.net/10722/272136 |
ISSN | 2023 Impact Factor: 3.9 2023 SCImago Journal Rankings: 1.058 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Jin, K | - |
dc.contributor.author | Li, X | - |
dc.date.accessioned | 2019-07-20T10:36:22Z | - |
dc.date.available | 2019-07-20T10:36:22Z | - |
dc.date.issued | 2018 | - |
dc.identifier.citation | Chemistry - A European Journal, 2018, v. 24 n. 66, p. 17397-17404 | - |
dc.identifier.issn | 0947-6539 | - |
dc.identifier.uri | http://hdl.handle.net/10722/272136 | - |
dc.description.abstract | Cysteine‐based native chemical ligation (NCL) has been a very powerful approach for convergent synthesis of peptides and proteins. However, owing to the low abundance of cysteine (Cys) in proteins, applications of NCL in protein chemical synthesis are limited. To expand the peptide ligation toolbox, NCL followed by desulfurization has been developed to enable peptide ligation at Xaa‐Ala conjunctions, that is, formal “alanine ligation”. In this regard, effective peptide desulfurization methods are critical. This Concept article summarizes the development of different desulfurization strategies for peptide and protein chemical synthesis. | - |
dc.language | eng | - |
dc.publisher | Wiley - VCH Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www.wiley-vch.de/home/chemistry | - |
dc.relation.ispartof | Chemistry - A European Journal | - |
dc.subject | Cysteine surrogates | - |
dc.subject | Desulfurization | - |
dc.subject | Native chemical ligation (NCL) | - |
dc.subject | One-pot synthesis | - |
dc.subject | Proteins | - |
dc.title | Advances in Native Chemical Ligation-Desulfurization: A Powerful Strategy for Peptide and Protein Synthesis | - |
dc.type | Article | - |
dc.identifier.email | Li, X: xuechenl@hku.hk | - |
dc.identifier.authority | Li, X=rp00742 | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/chem.201802067 | - |
dc.identifier.pmid | 29947435 | - |
dc.identifier.scopus | eid_2-s2.0-85054558561 | - |
dc.identifier.hkuros | 299159 | - |
dc.identifier.volume | 24 | - |
dc.identifier.issue | 66 | - |
dc.identifier.spage | 17397 | - |
dc.identifier.epage | 17404 | - |
dc.identifier.isi | WOS:000451901200003 | - |
dc.publisher.place | Germany | - |
dc.identifier.issnl | 0947-6539 | - |