Structural insight into Parkinson's disease treatment from drug-inhibited DOPA decarboxylase.

Abstract

DOPA decarboxylase (DDC) is responsible for the synthesis of the key neurotransmitters dopamine and serotonin via decarboxylation of L-3,4-dihydroxyphenylalanine (L-DOPA) and L-5-hydroxytryptophan, respectively. DDC has been implicated in a number of clinic disorders, including Parkinson's disease and hypertension. Peripheral inhibitors of DDC are currently used to treat these diseases. We present the crystal structures of ligand-free DDC and its complex with the anti-Parkinson drug carbiDOPA. The inhibitor is bound to the enzyme by forming a hydrazone linkage with the cofactor, and its catechol ring is deeply buried in the active site cleft. The structures provide the molecular basis for the development of new inhibitors of DDC with better pharmacological characteristics.

• Authors: P Burkhard, P Dominici, C Borri-Voltattorni, J N Jansonius, V N Malashkevich
• Journal: Nature structural biology (Nat Struct Biol) Vol. 8 Issue 11 Pg. 963-7 (Nov 2001) ISSN: 1072-8368 [Print] United States
• PMID: 11685243 (Publication Type: Journal Article)

Chemical References

• Antiparkinson Agents
• Aromatic Amino Acid Decarboxylase Inhibitors
• Ligands
• Levodopa
• Benserazide
• 5-Hydroxytryptophan
• Dopa Decarboxylase
• Carbidopa

Topics

• 5-Hydroxytryptophan (chemistry, metabolism)
• Animals
• Antiparkinson Agents (chemistry, metabolism, pharmacology)
• Aromatic Amino Acid Decarboxylase Inhibitors
• Benserazide (chemistry, pharmacology)
• Binding Sites
• Carbidopa (chemistry, metabolism, pharmacology)
• Crystallography, X-Ray
• Dopa Decarboxylase (chemistry, metabolism)
• Drug Design
• Humans
• Kidney (enzymology)
• Levodopa (chemistry, metabolism)
• Ligands
• Models, Molecular
• Parkinson Disease (drug therapy, enzymology)
• Pliability
• Protein Structure, Secondary
• Swine