TY - JOUR
T1 - The Mass Distance Fingerprint: A statistical framework for de novo detection of predominant modifications using high-accuracy mass spectrometry
AU - Potthast, Frank
AU - Gerrits, Bertran
AU - Häkkinen, Jari
AU - Rutishauser, Dorothea
AU - Ahrens, Christian H.
AU - Roschitzki, Bernd
AU - Baerenfaller, Katja
AU - Munton, Richard P.
AU - Walther, Pascal
AU - Gehrig, Peter
AU - Seif, Philipp
AU - Seebergerg, Peter H.
AU - Schlapbach, Ralph
PY - 2007
Y1 - 2007
N2 - We describe a statistical measure, Mass Distance Fingerprint, for automatic de novo detection of predominant peptide mass distances, i.e., putative protein modifications. The method's focus is to globally detect mass differences, not to assign peptide sequences or modifications to individual spectra. The Mass Distance Fingerprint is calculated from high accuracy measured peptide masses. For the data sets used in this study, known mass differences are detected at electron mass accuracy or better. The proposed method is novel because it works independently of protein sequence databases and without any prior knowledge about modifications. Both modified and unmodified peptides have to be present in the sample to be detected. The method can be used for automated detection of chemical/post-translational modifications, quality control of experiments and labeling approaches, and to control the modification settings of protein identification tools. The algorithm is implemented as a web application and is distributed as open source software.
AB - We describe a statistical measure, Mass Distance Fingerprint, for automatic de novo detection of predominant peptide mass distances, i.e., putative protein modifications. The method's focus is to globally detect mass differences, not to assign peptide sequences or modifications to individual spectra. The Mass Distance Fingerprint is calculated from high accuracy measured peptide masses. For the data sets used in this study, known mass differences are detected at electron mass accuracy or better. The proposed method is novel because it works independently of protein sequence databases and without any prior knowledge about modifications. Both modified and unmodified peptides have to be present in the sample to be detected. The method can be used for automated detection of chemical/post-translational modifications, quality control of experiments and labeling approaches, and to control the modification settings of protein identification tools. The algorithm is implemented as a web application and is distributed as open source software.
KW - modification
KW - Mass Distance Histogram
KW - post-translational
KW - protein identification
KW - Mass Distance Fingerprint
U2 - 10.1016/j.jchromb.2007.04.020
DO - 10.1016/j.jchromb.2007.04.020
M3 - Article
SN - 1873-376X
VL - 854
SP - 173
EP - 182
JO - Journal of Chromatography. B
JF - Journal of Chromatography. B
IS - 1-2
ER -