| Literature DB >> 32818002 |
Rosemary I Adaba1, Greg Mann2, Andrea Raab3, Wael E Houssen1,4,5, Andrew R McEwan1,4, Louise Thomas1,4, Jioji Tabudravu1, James H Naismith2, Marcel Jaspars1.
Abstract
There is a growing interest in the use of cyclic peptides as therapeutics, but their efficient production is often the bottleneck in taking them forward in the development pipeline. We have recently developed a method to synthesise azole-containing cyclic peptides using enzymes derived from different cyanobactin biosynthetic pathways. Accurate quantification is crucial for calculation of the reaction yield and for the downstream biological testing of the products. In this study, we demonstrate the development and validation of two methods to accurately quantify these compounds in the reaction mixture and after purification. The first method involves the use of a HPLC coupled in parallel to an ESMS and an ICPMS, hence correlating the calculated sulfur content to the amount of cyclic peptide. The second method is an NMR ERETIC method for quantifying the solution concentration of cyclic peptides. These methods make the quantification of new compounds much easier as there is no need for the use of authentic standards when they are not available.Entities:
Keywords: Cyanobacteria; Cyclic peptide; ICP-MS; LC-MS; NMR; Quantification without authentic standards; qNMR
Year: 2016 PMID: 32818002 PMCID: PMC7115945 DOI: 10.1016/j.tet.2016.11.040
Source DB: PubMed Journal: Tetrahedron ISSN: 0040-4020 Impact factor: 2.457