Recent extensions to native chemical ligation for the chemical synthesis of peptides and proteins
| Field | Value | Language |
| dc.contributor.author | Malins, Lara R. | |
| dc.contributor.author | Payne, Richard J. | |
| dc.date.accessioned | 2020-06-19 | |
| dc.date.available | 2020-06-19 | |
| dc.date.issued | 2014-10-03 | |
| dc.identifier.uri | https://www.sciencedirect.com/science/article/pii/S1367593114001306 | |
| dc.identifier.uri | https://hdl.handle.net/2123/22607 | |
| dc.description.abstract | Native chemical ligation continues to play a pivotal role in the synthesis of increasingly complex peptide and protein targets twenty years after its initial report. This opinion article will highlight a number of recent, powerful extensions of the technology that have expanded the scope of the reaction, accelerated ligation rates, enabled chemoselective post-ligation modifications, and streamlined the ligation of multiple peptide fragments. These advances have facilitated the synthesis of a number of impressive protein targets to date and hold great promise for the continued application of native chemical ligation for the detailed study of protein structure and function. | en |
| dc.language.iso | en_US | en |
| dc.publisher | Elsevier | en |
| dc.relation | ARC FT130100150 | en |
| dc.rights | Other | en |
| dc.title | Recent extensions to native chemical ligation for the chemical synthesis of peptides and proteins | en |
| dc.type | Article | en |
| dc.subject.asrc | FoR::030599 - Organic Chemistry not elsewhere classified | en |
| dc.identifier.doi | 10.1016/j.cbpa.2014.09.021 | |
| dc.type.pubtype | Author accepted manuscript | en |
| dc.relation.arc | FT130100150 | |
| usyd.faculty | SeS faculties schools::Faculty of Science | en |
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