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PIPI2: Sensitive Tag-Based Database Search to Identify Peptides with Multiple Post-translational Modifications.
Lai, Shengzhi; Zhao, Peize; Zhou, Chen; Li, Ning; Yu, Weichuan.
Afiliación
  • Lai S; Department of Electronic and Computer Engineering, The Hong Kong University of Science and Technology, Hong Kong, Hong Kong, China.
  • Zhao P; Interdisciplinary Programs Office, The Hong Kong University of Science and Technology, Hong Kong, Hong Kong, China.
  • Zhou C; Department of Electronic and Computer Engineering, The Hong Kong University of Science and Technology, Hong Kong, Hong Kong, China.
  • Li N; Shenzhen-Hong Kong Collaborative Innovation Research Institute, HKUST, Futian, Shenzhen 518000, China.
  • Yu W; Division of Life Science, The Hong Kong University of Science and Technology, Hong Kong, Hong Kong, China.
J Proteome Res ; 23(6): 1960-1969, 2024 Jun 07.
Article en En | MEDLINE | ID: mdl-38770571
ABSTRACT
Peptide identification is important in bottom-up proteomics. Post-translational modifications (PTMs) are crucial in regulating cellular activities. Many database search methods have been developed to identify peptides with PTMs and characterize the PTM patterns. However, the PTMs on peptides hinder the peptide identification rate and the PTM characterization precision, especially for peptides with multiple PTMs. To address this issue, we present a sensitive open search engine, PIPI2, with much better performance on peptides with multiple PTMs than other methods. With a greedy approach, we simplify the PTM characterization problem into a linear one, which enables characterizing multiple PTMs on one peptide. On the simulation data sets with up to four PTMs per peptide, PIPI2 identified over 90% of the spectra, at least 56% more than five other competitors. PIPI2 also characterized these PTM patterns with the highest precision of 77%, demonstrating a significant advantage in handling peptides with multiple PTMs. In the real applications, PIPI2 identified 30% to 88% more peptides with PTMs than its competitors.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptidos / Procesamiento Proteico-Postraduccional / Bases de Datos de Proteínas / Proteómica / Motor de Búsqueda Límite: Humans Idioma: En Revista: J Proteome Res Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Péptidos / Procesamiento Proteico-Postraduccional / Bases de Datos de Proteínas / Proteómica / Motor de Búsqueda Límite: Humans Idioma: En Revista: J Proteome Res Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article País de afiliación: China
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