Mogjib Salek, PhD

Postdoctoral Scientist


Phone: +49 6221 42 3823


Scientific CV

Since Oct 2017
Postdoctoral scientist, Immunotherapy and Immunoprevention, DKFZ, Heidelberg

Scientist, Large Scale Biology (EDyP, BGE), Biosciences and Biotechnology Institute of Grenoble (BIG), France

Consultant in Proteomics, Toulouse, France

Research fellow, T Cell Signaling Group, Sir William Dunn School of Pathology, University of Oxford, UK

Postdoctoral fellow, Institute of European Oncology – FIRC Institute of Molecular Oncology Foundation (IEO-IFOM), Milan, Italy

PhD student, Central Spectroscopy Unit (Prof. Lehmann), DKFZ, Heidelberg

Research Project

Mass spectrometry-based identification of mutation-derived tumor neoepitopes

To differentiate tumor cells from normal cells, the immune system needs to recognize structures that are tumor-specific. Altered proteins resulting from tumor-specific mutations – so-called neoantigens - fulfil this requirement, and are thus attractive targets for immunotherapy approaches. However, it is not yet clear which epitopes derived from neoantigens (i.e. “neoepitopes”) are actually presented to the immune system on the tumor cell surface, as they mostly are of low abundance and therefore difficult to detect. But only presented neoepitopes represent meaningful targets for epitope-specific vaccines or adoptive transfer of T cells with transgenic T cell receptors.

A targeted mass spectrometry (MS) approach has been developed in the lab to detect low abundance epitopes. It has successfully been applied to detect neoepitopes. The current research project aims at establishing a high-throughput neoepitope detection workflow using the most recent mass spectrometry technology and advanced bioinformatics. The workflow will be applicable for every tumor for which the tumor-specific mutations have been identified by genome sequencing, and for which samples are available for MS analysis.

The ultimate aim of the project is to provide a rational basis for the development of future immunotherapies by providing validated target neoepitopes.

Resulting Publications

A targeted LC-MS strategy for low-abundant HLA class-I-presented peptide detection identifies novel human papillomavirus T-cell epitopes.
Blatnik R*, Mohan N*, Bonsack M*, Falkenby LG, Hoppe S, Josef K, Steinbach A, Becker S, Nadler WM, Rucevic M, Larsen MR, Salek M, Riemer AB. * Equal contributors.
Proteomics 2018, 18(11): e1700390.

Previous Publications

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