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Therapeutic intervention based on protein prenylation and associated modifications

Journal

NATURE CHEMICAL BIOLOGY
Volume 2, Issue 10, Pages 518-528

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/nchembio818

Keywords

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Funding

  1. NCI NIH HHS [CA41996, P01 CA032737, R01 CA041996, CA32737] Funding Source: Medline
  2. NIAID NIH HHS [R01 AI054384, AI054384, R01 AI054384-17] Funding Source: Medline
  3. NIGMS NIH HHS [R01 GM041223, GM41223] Funding Source: Medline

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In eukaryotic cells, a specific set of proteins are modified by C-terminal attachment of 15-carbon farnesyl groups or 20-carbon geranylgeranyl groups that function both as anchors for fixing proteins to membranes and as molecular handles for facilitating binding of these lipidated proteins to other proteins. Additional modification of these prenylated proteins includes C-terminal proteolysis and methylation, and attachment of a 16-carbon palmitoyl group; these modifications augment membrane anchoring and alter the dynamics of movement of proteins between different cellular membrane compartments. The enzymes in the protein prenylation pathway have been isolated and characterized. Blocking protein prenylation is proving to be therapeutically useful for the treatment of certain cancers, infection by protozoan parasites and the rare genetic disease Hutchinson-Gilford progeria syndrome.

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