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Mathias Mann
Matthias Mann, a German native, was trained in physics and mathematics
and studied with John Fenn for his Ph.D. which he received from Yale
University in 1989. After postdoctoral work with Peter Roepstorff in
Denmark, he became group leader at the European Molecular Biology
Laboratory (EMBL) in Heidelberg, Germany. Since 1998 he has been full
professor at the University of Southern Denmark, Odense where he is now
the director of the Center for Experimental BioInformatics (CEBI). From
July 2005 he will be a director at the Max-Planck Institute for
Biochemistry in Martinsried, near Munich.
Dr. Mann’s work in mass spectrometry and proteomics stretches back for
20 years, starting with work on the electrospray ionization method and
today encompasses a wide spectrum of cell signaling problems which his
group approaches with proteomic techniques. He has been elected member
of the European Molecular Biology Laboratory (EMBO), visiting professor
at Harvard Medical School as well as to the Danish Society of Arts and
Sciences. He is author or co-author of more than 250 publications and
is the recipient of many international prizes.
Summary of work
Matthias Mann has been involved in mass spectrometry based proteomics
from the very beginning. As a graduate student with John Fenn at Yale
University, he was a member of the team that developed electrospray, a
key technology that won the Nobel prize for John Fenn in 2002. Later,
his group at the European Molecular Biology Laboratory pioneered a set
of technologies consisting of the first algorithm to identify peptides
in sequence databases by their mass spectrometric fragmentation spectra
(‘Peptide Sequence Tag’ algorithm), a method to make small amounts of
gel separated proteins amenable to mass spectrometry and a
miniaturized, highly efficient version of electrospray working at
extremely low flow rates (‘nanoelectrospray’). This allowed extremely
sensitive protein sequencing and resulted in the cloning of important
biological molecules such as the catalytic subunit of telomerase and
Caspase-8. His group also performed the first, large scale
identification of proteins linking ‘proteome’ to genome for the first
time. His group also initiated work on protein-protein interaction
detection by mass spectrometry and first used mass spectrometry to
characterize multi-protein complexes. Recently, Dr. Mann’s group
described a quantitative proteomics technology termed Stable Isotope
Labeling with Amino acids in Cell culture or SILAC. The SILAC
technology has been applied to signal dependent protein – protein
interactions and to quantify relative changes in phosphorylation upon
signaling. By comparing several states, SILAC has allowed the protein
composition of the human nucleolus in response to perturbation to be
determined and allowed mapping the time-order of activation in
signaling pathways. These developments now allow proteomics to study
dynamic processes. |
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