Atypical alpha-Conotoxin LtIA from Conus litteratus Targets a Novel Microsite of the alpha 3 beta 2 Nicotinic Receptor

作者：Luo, Sulan^*; Akondi, Kalyana Bharati; Zhangsun, Dongting; Wu, Yong; Zhu, Xiaopeng; Hu, Yuanyan; Christensen, Sean; Dowell, Cheryl; Daly, Norelle L.; Craik, David J.; Wang, Ching-I. Anderson; Lewis, Richard J.; Alewood, Paul F.; McIntosh, J. Michael

来源：JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285(16): 12355-12366.

DOI：10.1074/jbc.M109.079012

• PROTEIN SECONDARY STRUCTURE
• NACHR SUBTYPE SELECTIVITY
• ACETYLCHOLINE-RECEPTORS
• CRYSTAL-STRUCTURE
• NMR-SPECTROSCOPY
• BINDING PROTEIN
• HOMOLOG ACHBP
• CDNA CLONING
• PEPTIDE
• SUBUNIT

Different nicotinic acetylcholine receptor (nAChR) subtypes are implicated in learning, pain sensation, and disease states, including Parkinson disease and nicotine addiction. alpha-Conotoxins are among the most selective nAChR ligands. Mechanistic insights into the structure, function, and receptor interaction of alpha-conotoxins may serve as a platform for development of new therapies. Previously characterized alpha-conotoxins have a highly conserved Ser-Xaa-Pro motif that is crucial for potent nAChR interaction. This study characterized the novel alpha-conotoxin LtIA, which lacks this highly conserved motif but potently blocked alpha 3 beta 2 nAChRs with a 9.8 nM IC50 value. The off-rate of LtIA was rapid relative to Ser-Xaa-Pro-containing alpha-conotoxin MII. Nevertheless, pre-blockof alpha 3 beta 2 nAChRs with LtIA prevented the slowly reversible block associated with MII, suggesting overlap in their binding sites. nAChR beta subunit ligand-binding interface mutations were used to examine the > 1000-fold selectivity difference of LtIA for alpha 3 beta 2 versus alpha 3 beta 4 nAChRs. Unlike MII, LtIA had a > 900-fold increased IC50 value on alpha 3 beta 2(F119Q) versus wild type nAChRs, whereas T59K and V111I beta 2 mutants had little effect. Molecular docking simulations suggested that LtIA had a surprisingly shallow binding site on the alpha 3 beta 2 nAChR that includes beta 2 Lys-79. The K79A mutant disrupted LtIA binding but was without effect on an LtIA analog where the Ser-Xaa-Pro motif is present, consistent with distinct binding modes.

• 出版日期2010-4-16
• 单位海南大学