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Institute of Medical Biotechnology
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  1. Friedrich-Alexander-Universität
  2. Technische Fakultät
  3. Department Chemie- und Bioingenieurwesen

Institute of Medical Biotechnology

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  5. Identification of transporters of the MGC-basic proteins

Identification of transporters of the MGC-basic proteins

Bereichsnavigation: Research
  • Research Groups
    • Muscle Opto-Biomechatronics
      • The MyoRobot
      • The MechaMorph
      • The IsoStretcher
      • Virtual Laboratory
    • Malaria Biotechnology
      • RG Protein Engineering
      • Metabolic enzymes as drug targets
      • Identification of novel antimalarial compounds
      • Mitosis as drug target
      • Identification of transporters of the MGC-basic proteins
      • Characterization of drug-resistance transporters of the digestive vacuole
      • Malaria vaccine directed against blood stages
    • Tissue Engineering
      • Bone Tissue Engineering
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      • Research Topic 3 (TE)
    • Optical Technologies in Life Sciences
      • Label-free Multiphoton Imaging
      • Multiphoton Endomicroscopy for Life Science and Medicine
      • Raman Spectroscopy of Biological Tissue
      • PiezoGRIN: Multiphoton Imaging under high Pressures
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      • High-throughput Biology & Functional Neurogenomics
      • Robophotonics & Rapid Prototyping
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Identification of transporters of the MGC-basic proteins

Group Leader

Barbara Kappes

Prof. Dr. Barbara Kappes

Group Leader

Medical Biotechnology
Malaria Biotechnology

Raum: Room 01.020
Paul-Gordan-Str. 3
91052 Erlangen
Germany
  • Telefon: +49913185-23299
  • E-Mail: barbara.kappes@fau.de
  • Webseite: https://www.mbt.tf.fau.de/
Nina Simon

Dr. Nina Simon

Group Leader

Medical Biotechnology
Malaria Biotechnology

Raum: Room 00.115
Ulrich-Schalk-Str. 3
91056 Erlangen
Germany
  • Telefon: +49913185-69657
  • E-Mail: nina.simon@fau.de

During its intraerythrocytic growth, the parasite secretes a group of proteins that do not contain the common PEXEL export motif but instead have a membrane binding motif in common, the so-called MGC-basic motif, which is responsible for their translocation into the parasitophorous vacuole and the erythrocyte cytoplasm. Many of these proteins are signaling proteins (a picture with two of differently fluorescently labeled MGC-basic proteins within the parasite is shown below) and most likely involved in signaling events that occur outside of the constraints of the parasite plasma membrane. Up to now, it is not known how the MGC-basic proteins are translocated over the parasite membrane into the parasitophorous vacuole (Möskes et al., 2004). However, blocking the function of the supposed transporter will most likely result in a deregulation of signaling events required to build up and maintain the parasite`s highly dynamic tubovesicular network within in the erythrocyte and thus will finally result in the death of the parasite.

Friedrich-Alexander-Universität
Erlangen-Nürnberg

Schlossplatz 4
91054 Erlangen
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