Challenges in the use of sortase and other peptide ligases for site-specific protein modification. (5th May 2022)

• Record Type: Journal Article
• Authors: Morgan, Holly E.; Turnbull, W. Bruce; Webb, Michael E.
• Is Part Of: Chemical Society reviews. Volume 51:Number 10(2022)
• Page Start: 4121
• Page End: 4145
• Publication Date: 2022-05-05
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/d0cs01148g
• Languages: English
• ISSNs: 0306-0012

Abstract

Abstract : We highlight chemical and biochemical strategies taken to optimise peptide and protein modification using peptide ligases. Abstract : Site-specific protein modification is a widely-used biochemical tool. However, there are many challenges associated with the development of protein modification techniques, in particular, achieving site-specificity, reaction efficiency and versatility. The engineering of peptide ligases and their substrates has been used to address these challenges. This review will focus on sortase, peptidyl asparaginyl ligases (PALs) and variants of subtilisin; detailing how their inherent specificity has been utilised for site-specific protein modification. The review will explore how the engineering of these enzymes and substrates has led to increased reaction efficiency mainly due to enhanced catalytic activity and reduction of reversibility. It will also describe how engineering peptide ligases to broaden their substrate scope is opening up new opportunities to expand the biochemical toolkit, particularly through the development of techniques to conjugate multiple substrates site-specifically onto a protein using orthogonal peptide ligases.