The engineering of an orally active conotoxin for the treatment of neuropathic pain

RJ Clark, J Jensen, ST Nevin, BP Callaghan… - Angewandte …, 2010 - infona.pl
Heilendes Gift: Peptide aus dem Gift der Kegelschnecke sind potenzielle Therapeutika zur
Behandlung von neuropathischem Schmerz. Ein Nachteil dieser Peptide ist ihre kurze …

Engineering stable peptide toxins by means of backbone cyclization: stabilization of the α-conotoxin MII

…, NL Daly, KJ Rosengren, ST Nevin… - Proceedings of the …, 2005 - National Acad Sciences
Conotoxins (CTXs), with their exquisite specificity and potency, have recently created much
excitement as drug leads. However, like most peptides, their beneficial activities may …

[HTML][HTML] α-Selenoconotoxins, a new class of potent α7 neuronal nicotinic receptor antagonists

CJ Armishaw, NL Daly, ST Nevin, DJ Adams… - Journal of Biological …, 2006 - ASBMB
Disulfide bonds are important structural motifs that play an essential role in maintaining the
conformational stability of many bioactive peptides. Of particular importance are the …

[HTML][HTML] The synthesis, structural characterization, and receptor specificity of the α-conotoxin Vc1. 1

RJ Clark, H Fischer, ST Nevin, DJ Adams… - Journal of biological …, 2006 - ASBMB
The α-conotoxin Vc1.1 is a small disulfide-bonded peptide currently in development as a
treatment for neuropathic pain. This study describes the synthesis, determination of the …

Solving the α-conotoxin folding problem: efficient selenium-directed on-resin generation of more potent and stable nicotinic acetylcholine receptor antagonists

…, ST Nevin, AA Grishin, ST Ngo… - Journal of the …, 2010 - ACS Publications
α-Conotoxins are tightly folded miniproteins that antagonize nicotinic acetylcholine
receptors (nAChR) with high specificity for diverse subtypes. Here we report the use of …

Tissue‐type plasminogen activator requires a co‐receptor to enhance NMDA receptor function

AL Samson, ST Nevin, D Croucher… - Journal of …, 2008 - Wiley Online Library
Glutamate is the main excitatory neurotransmitter of the CNS. Tissue‐type plasminogen
activator (tPA) is recognized as a modulator of glutamatergic neurotransmission. This attribute is …

Are α9α10 nicotinic acetylcholine receptors a pain target for α-conotoxins?

ST Nevin, RJ Clark, H Klimis, MJ Christie, DJ Craik… - Molecular …, 2007 - ASPET
The synthetic α-conotoxin Vc1.1 is a small disulfide bonded peptide currently in development
as a treatment for neuropathic pain. Unlike Vc1.1, the native post-translationally modified …

[HTML][HTML] Scanning mutagenesis of α-conotoxin Vc1. 1 reveals residues crucial for activity at the α9α10 nicotinic acetylcholine receptor

R Halai, RJ Clark, ST Nevin, JE Jensen… - Journal of biological …, 2009 - ASBMB
Vc1.1 is a disulfide-rich peptide inhibitor of nicotinic acetylcholine receptors that has stimulated
considerable interest in these receptors as potential therapeutic targets for the treatment …

Total synthesis of the analgesic conotoxin MrVIB through selenocysteine‐assisted folding

AD de Araujo, B Callaghan, ST Nevin, NL Daly… - Angewandte Chemie …, 2011 - infona.pl
Secs for your folding problems: Selenocysteine (Sec) residues were used to drive the
folding of conotoxin MrVIB, a previously “unfoldable” miniprotein with therapeutic potential (see …

[HTML][HTML] Identification of a novel class of nicotinic receptor antagonists: dimeric conotoxins VxXIIA, VxXIIB, and VxXIIC from Conus vexillum

…, A Nicke, A Jones, CI Schroeder, ST Nevin… - Journal of biological …, 2006 - ASBMB
The venoms of predatory marine snails (Conus spp.) contain diverse mixtures of peptide
toxins with high potency and selectivity for a variety of voltage-gated and ligand-gated ion …