Abstract
Orexin-A and orexin-B (hypocretin-1 and hypocretin-2, respectively) are important hypothalamic neuro-peptides, which are encoded by a single mRNA transcript and stimulate food intake as well as regulate wakefulness. Here we determined the solution structure of orexin-A by NMR spectroscopy and by simulated-annealing calculation. The structural features of orexin-A involve two α-helices, with the hydrophobic residues disposed to on one side of helix, and hydrophilic residues to the other. A hydrophilic turn induced by two disulfide bonds provides the key difference between orexin-A and -B. With previous mutagenic studies, the derived structure of orexin-A provides us with a structure-functional view for novel drug design.
Original language | English |
---|---|
Pages (from-to) | 565-573 |
Number of pages | 9 |
Journal | Journal of biochemistry and molecular biology |
Volume | 37 |
Issue number | 5 |
DOIs | |
Publication status | Published - 2004 Sept |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Molecular Biology