peptide sequencing for large-scale proteomics remains challenging because of the lack of full coverage of ion series in tandem mass spectra. We developed a mirror protease of trypsin, acetylated LysargiNase (Ac-LysargiNase), with superior activity and stability. The mirror spectrum pairs derived from the Ac-LysargiNase and trypsin treated samples can generate full and ion series, which provide mutual complementarity of each other, and allow us to develop a novel algorithm, pNovoM, for sequencing.
View Article and Find Full Text PDFMotivation: Proteogenomics has been well accepted as a tool to discover novel genes. In most conventional proteogenomic studies, a global false discovery rate is used to filter out false positives for identifying credible novel peptides. However, it has been found that the actual level of false positives in novel peptides is often out of control and behaves differently for different genomes.
View Article and Find Full Text PDFZhongguo Zhong Xi Yi Jie He Za Zhi
October 2003