Evaluation of the site-unspecified peptide identification method for proteolytic peptide mapping. Issue 61 (7th October 2020)

• Record Type: Journal Article
• Authors: Wang, H. B.; Zeng, F.; Wang, Y. Y.; Li, X.; S. H., ; Li, Y. M.; Wang, Y. F.; Liu, Y. H.; Lu, F. P.
• Is Part Of: RSC advances. Volume 10:Issue 61(2020)
• Page Start: 37182
• Page End: 37186
• Publication Date: 2020-10-07
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0ra04226a
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : The site-unspecific method could successfully identify most of the peptides from tryptic hydrolysates revealed by site-specific identification. Abstract : Proteases are widely used in the food industry to hydrolyze proteins and prepare bioactive peptides. Peptide mapping identification supports the application of proteases in the food industry. The site-specified peptide identification method, which was developed for site-specific proteases like trypsin, is relatively mature and reliable but cannot be applied using most industrial proteases with weak site specificity. To address this issue, the performance and reliability of the site-unspecified peptide identification method should be investigated and evaluated. In this study, tryptic hydrolysates of a single protein and a protein mixture were used to evaluate the site-unspecified identification method. The species origin of the hydrolyzed proteins was not specified in a database search, meaning that millions of protein sequences were included for calculating and matching. At least 98% of the tryptic peptides were successfully identified via the site-unspecified method, demonstrating that the site-unspecified method shows promising reliability. Moreover, the site-unspecified method identified more peptides than the site-specified method, including those from the low-frequency site-unspecific hydrolysis of trypsin, suggesting that the method has strong capabilities for peptide mapping. The results indicate the applicability of the site-unspecified peptide identification method in the study of site-unspecific industrial proteases.