Study of Mutant Proteins With Folding Defects in Cultured Patient Cells

  • Gabriele Dodt
  • Claudia Walter
Part of the Methods in Molecular Biology™ book series (MIMB, volume 232)


The example used in this chapter concerns the group of autosomal recessive inherited peroxisome biogenesis disorders (PBDs). These disorders are genetically heterogeneous with at least 12 different complementation groups (CGs). CG 1 is the largest characterized by mutations in HsPEX1, a gene encoding a 143 kD AAA protein (ATPases associated with diverse cellular activities) (1, 2, 3). About 65% of the PBD patients suffering from peroxisome biogenesis disorders harbor mutations in PEX1 (4, 5, 6). Although the function of PEX1 is not defined yet, it is likely that PEX1 plays a significant role in the import of peroxisomal matrix proteins from the cytosol—where they are translated—into the peroxisomes (1,2,7,8).


Sodium Dodecyl Sulfate G843D Mutation Zellweger Syndrome Folding Defect Peroxisome Biogenesis Disorder 
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Copyright information

© Humana Press Inc., Totowa, NJ 2003

Authors and Affiliations

  • Gabriele Dodt
    • 1
  • Claudia Walter
    • 2
  1. 1.Physiologisch-Chemisches InstitutEberhard Karls Universität TübingenTübingenGermany
  2. 2.Institut für Physiologische ChemieRuhr-Universität BochumBochumGermany

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