Conotoxins and Drug Discovery With Special Reference to Hainan Species

Luo, Sulan; Zhu, Xiaopeng; Zhangsun, Dongting

doi:10.1007/978-94-007-6726-3_21-1

Cited by 1 publication

(2 citation statements)

References 112 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…Conus is a genus of marine gastropod molluscs which is estimated to have 700 different species distributing in tropical and sub-tropical oceans [9,10]. These gastropods armed with deadly venoms can capture worms, fishes or other mollusks.…”

Section: Introductionmentioning

confidence: 99%

“…Based on their conserved signal peptide sequences, the various conotoxins are classified into different super families. Further classification into families depends on their patterns of disulfide and pharmacological activities [10,13,14]. Among the conotoxins, α-conotoxins are the most studied and targeted muscle-type or neuronal-type nAChRs with high affinity and selectivity.…”

Section: Introductionmentioning

confidence: 99%

See 1 more Smart Citation

Alanine-Scanning Mutagenesis of α-Conotoxin GI Reveals the Residues Crucial for Activity at the Muscle Acetylcholine Receptor

Ning

Ren

et al. 2018

Marine Drugs

Self Cite

View full text Add to dashboard Cite

Recently, the muscle-type nicotinic acetylcholine receptors (nAChRs) have been pursued as a potential target of several diseases, including myogenic disorders, muscle dystrophies and myasthenia gravis, etc. α-conotoxin GI isolated from Conus geographus selectively and potently inhibited the muscle-type nAChRs which can be developed as a tool to study them. Herein, alanine scanning mutagenesis was used to reveal the structure–activity relationship (SAR) between GI and mouse α1β1δε nAChRs. The Pro5, Gly8, Arg9, and Tyr11 were proved to be the critical residues for receptor inhibiting as the alanine (Ala) replacement led to a significant potency loss on mouse α1β1δε nAChR. On the contrary, substituting Asn4, His10 and Ser12 with Ala respectively did not affect its activity. Interestingly, the [E1A] GI analogue exhibited a three-fold potency for mouse α1β1δε nAChR, whereas it obviously decreased potency at rat α9α10 nAChR compared to wildtype GI. Molecular dynamic simulations also suggest that loop2 of GI significantly affects the interaction with α1β1δε nAChR, and Tyr11 of GI is a critical residue binding with three hydrophobic amino acids of the δ subunit, including Leu93, Tyr95 and Leu103. Our research elucidates the interaction of GI and mouse α1β1δε nAChR in detail that will help to develop the novel analogues of GI.

show abstract

Section: Introductionmentioning

confidence: 99%