• 1986 - 1992 Biology at the Universities of Bayreuth and Tübingen
• 1992 - 1996 PhD student in the laboratory of Walter Neupert at the Department of Physiological Chemistry in Munich
• 1996 - 1998 Postdoc in the laboratory of Randy Schekman at the University of California in Berkeley, USA
• 1999 - 2006 Group leader (wissenschaftlicher Assistent) in the Department of Physiological Chemistry at the Adolf-Butenandt Institute in Munich
• 2006 - Arnold Sommerfeld Award of the Bavarian Academy of Sciences
• since 2006 - Professor of Cell Biology, Faculty of Biology, University of Kaiserslautern. Head of the Department
• 2008 - Personal Teaching Award, Rheinland-Pfalz
• Feb 2009 -  Feb 2012 Dean of the Biological Faculty
• 2010 - Award for Excellent Teaching in Rheinland-Pfalz
• 2011 - FEBS National Lecture Award, Brussels
• 2011-2017 - Spokesperson of the GBM studygroup Redox Biology
• 2015-2017 - Vice President of the GBM
• since 2016 Member of the DFG Panel Biochemistry (Fachkollegium 201)
• since 2017 - President of the GBM (German Society of Biochemistry and Molecular Biology)
  
• Membership on Editorial Boards of BBA-General Topics, of Biological Chemistry, and Microbial Cell

The focus of our group is the biogenesis of mitochondrial proteins. A small number of these proteins is synthesized on mitochondrial ribosomes. Owing to their hydrophobic nature, mitochondrial translation products are inserted into the inner membrane in cotranslational process which relies on the tight membrane binding of mitochondrial ribosomes. Most mitochondrial proteins are synthesized as precursors in the cytosol. How these precursors reach the mitochondrial outer membrane, how they are prevented from folding and aggregation and how they are degraded if their import fails are current questions in the lab.

Hansen KG, Aviram N, Laborenz J, Bibi C, Meyer M, Spang A, Schuldiner M, Herrmann JM. 2018. An ER surface retrieval pathway safeguards the import of mitochondrial membrane proteins in yeast. Science. 361, 1118-1122.

Peleh V, Cordat, E, Herrmann JM. 2016. Mia40 is a trans-site receptor that drives protein import into the mitochondrial intermembrane space by hydrophobic substrate binding. eLIFE 2016 Jun 25;5. pii: e16177. doi: 10.7554/eLife.16177

Beckmann R, Herrmann JM. 2015. Mitoribosome oddities. Science 348, 288-289

Pfeffer S, Woellhaf MW, Herrmann JM, Förster F. 2015. Organization of the mitochondrial translation machinery studied in situ by cryoelectron tomogrphy. Nature Commun. 6, 6019

Longen S, Woellhaf MW, Petrungaro C, Riemer J, Herrmann JM. 2014. The Disulfide Relay of the Intermembrane Space Oxidizes the Ribosomal Subunit Mrp10 on Its Transit into the Mitochondrial Matrix. Developmental Cell 28, 30-42

Weckbecker D, Longen S, Riemer J, Herrmann JM. 2012. Atp23 biogenesis reveals a chaperone-like folding activity of Mia40 in the IMS of mitochondria. EMBO J. 31, 4348-4358

Bien M, Longen S, Wagener N, Chwalla I, Herrmann JM, Riemer J. 2010. Mitochondrial Disulfide Bond Formation Is Driven by Intersubunit Electron Transfer in Erv1 and Proofread by Glutathione. Mol Cell 37, 516-528

Riemer J, Bulleid N, Herrmann JM. 2009. Disulfide formation in the ER and mitochondria: two solutions to a common process. Science 324, 1284-1287

Neupert W, Herrmann JM 2007. Translocation of Proteins into Mitochondria. Annu Rev Biochem 76, 723-749

Mesecke N, Terziyska N, Kozany C, Baumann F, Neupert W, Hell K, Herrmann JM. 2005. A disulfide relay system in the intermembrane space of mitochondria that mediates protein import. Cell 121, 1059-1069

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