Proteomics

Dataset Information

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TimsTOF Pro datasets for CCS prediction


ABSTRACT: The contribution of peptide amino-acid sequence to collision cross-section values (CCS) has been investigated using a dataset of ~134,000 peptides of four different charge states (1+ to 4+). The migration data collection was acquired using a two-dimensional LC/trapped ion mobility spectrometry/quadrupole/time-of-flight MS analysis of HeLa cell digests created using 7 different proteases and converted to CCS values. Following the previously reported modeling approaches using intrinsic size parameters, we extended this methodology to encode the position of individual residues within a peptide sequence. A generalized prediction model was built by dividing the dataset into 8 groups (four charges for both tryptic/non-tryptic peptides). Position dependent intrinsic size parameters were independently optimized for the eight subsets of peptides, resulting in prediction accuracy of ~0.98 for the entire population of peptides.

ORGANISM(S): Homo Sapiens (human)

SUBMITTER: Yasushi Ishihama 

PROVIDER: PXD021440 | JPOST Repository | Mon Sep 06 00:00:00 BST 2021

REPOSITORIES: jPOST

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Publications

Sequence-Specific Model for Predicting Peptide Collision Cross Section Values in Proteomic Ion Mobility Spectrometry.

Chang Chih-Hsiang CH   Yeung Darien D   Spicer Victor V   Ogata Kosuke K   Krokhin Oleg O   Ishihama Yasushi Y  

Journal of proteome research 20210616


The contribution of peptide amino acid sequence to collision cross section values (CCS) has been investigated using a dataset of ∼134 000 peptides of four different charge states (1+ to 4+). The migration data were acquired using a two-dimensional liquid chromatography (LC)/trapped ion mobility spectrometry/quadrupole/time-of-flight mass spectrometry (MS) analysis of HeLa cell digests created using seven different proteases and was converted to CCS values. Following the previously reported model  ...[more]

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