Literature DB >> 32501003

IsoSpec2: Ultrafast Fine Structure Calculator.

Mateusz K Łącki1, Dirk Valkenborg2,3,4,5, Michał P Startek6.   

Abstract

High-resolution mass spectrometry becomes increasingly available with its ability to resolve the fine isotopic structure of measured analytes. It allows for high-sensitivity spectral deconvolution, leading to less false-positive identifications. Analytes can be identified by comparing their theoretical isotopic signal with the observed peaks. Necessary calculations are, however, computationally demanding and lead to long processing times. For wheat (trictum oestivum) alone, Uniprot holds more than 142 000 candidate protein sequences. This is doubled upon sequence reversal for identification FDR estimation and further multiplied by performing in silico digestion into peptides. The same peptide might originate from more than one protein, which reduces the overall number of sequences to be calculated. However, it is still huge. IsoSpec2 can perform these calculations fast. Compared to IsoSpec1, the algorithm is simpler, orders of magnitude faster, and offers more flexibility for the developers of algorithms for raw data analysis. It is freely available under a 2-clause BSD license, with bindings for the C++, C, R, and Python programming languages.

Year:  2020        PMID: 32501003     DOI: 10.1021/acs.analchem.0c00959

Source DB:  PubMed          Journal:  Anal Chem        ISSN: 0003-2700            Impact factor:   6.986


  3 in total

1.  Fine Structure in Isotopic Peak Distributions Measured Using Fourier Transform Ion Cyclotron Resonance Mass Spectrometry: A Comparison between an Infinity ICR Cell and a Dynamically Harmonized ICR Cell.

Authors:  Jingsha Xu; Meng Li; Bryan Marzullo; Christopher A Wootton; Mark P Barrow; Peter B O'Connor
Journal:  J Am Soc Mass Spectrom       Date:  2022-06-28       Impact factor: 3.262

2.  Locality-sensitive hashing enables efficient and scalable signal classification in high-throughput mass spectrometry raw data.

Authors:  Konstantin Bob; David Teschner; Thomas Kemmer; David Gomez-Zepeda; Stefan Tenzer; Bertil Schmidt; Andreas Hildebrandt
Journal:  BMC Bioinformatics       Date:  2022-07-20       Impact factor: 3.307

3.  Light contamination in stable isotope-labelled internal peptide standards is frequent and a potential source of false discovery and quantitation error in proteomics.

Authors:  Mogjiborahman Salek; Jonas D Förster; Wolf-Dieter Lehmann; Angelika B Riemer
Journal:  Anal Bioanal Chem       Date:  2022-02-04       Impact factor: 4.142

  3 in total

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