Results 71 to 80 of about 1,038 (93)
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Molecular mechanisms of α-conotoxin [S9K]TxID selectively targeting the rat α3β4 nicotinic acetylcholine receptor

International Journal of Biological Macromolecules
α3β4 nicotinic acetylcholine receptor (nAChR) is a potential therapeutic target for the treatment of drug dependence and addiction, lung cancer, overeating and obesity and other disorders.
Jinpeng Yu, Shuqi Zhao, Jianying Dong
exaly   +2 more sources

Enhancing Stability and Albumin Binding Efficiency of α-Conotoxin GI through Fatty Acid Modification.

Biochemistry, 2023
α-Conotoxin GI is a competitive blocker of muscle-type acetylcholine receptors and holds the potential for being developed as a molecular probe or a lead compound for drug discovery.
Panpan Qi   +8 more
semanticscholar   +1 more source

Basic Residues at Position 11 of α-Conotoxin LvIA Influence Subtype Selectivity between α3β2 and α3β4 Nicotinic Receptors via an Electrostatic Mechanism.

ACS Chemical Neuroscience, 2023
Understanding the determinants of α-conotoxin (α-CTX) selectivity for different nicotinic acetylcholine receptor (nAChR) subtypes is a prerequisite for the design of tool compounds to study nAChRs.
Yves Haufe   +12 more
semanticscholar   +1 more source

Dissecting oxidative folding of conotoxins using 3D structures of cysteine mutants predicted by AlphaFold 3: A case study of α-conotoxin RgIA, χ-conotoxin CMrVIA and ω-conotoxin MVIIA-Gly.

Toxicon
The ability of AlphaFold 3 to accurately predict the 3D structure of polypeptides has been explored to investigate the oxidative folding steps of conotoxins.
K. Radhakrishna   +5 more
semanticscholar   +1 more source

Variable peptide processing of a Conus (Asprella) neocostatus α-conotoxin generates bioactive toxiforms that are potent against distinct nicotinic acetylcholine receptor subtypes.

Biochemical Pharmacology
Conusvenoms are composed of peptides that are commonly post-translationally modified, increasing their chemical diversity beyond what is encoded in the genome and enhancing their potency and selectivity. This study describes how PTMs alter an α-conotoxin'
C. M. Ramones   +11 more
semanticscholar   +1 more source

The α3β4 nAChR tissue distribution identified by fluorescent α-conotoxin [D11A]LvIA.

International Journal of Biological Macromolecules
α3β4, a vital subtype of neuronal nicotinic acetylcholine receptors (nAChRs), is widely distributed in the brain, ganglia, and adrenal glands, associated with addiction and neurological diseases.
Chenxing Xu   +8 more
semanticscholar   +1 more source

α-Conotoxin LvID, an antagonist of α7 nicotinic acetylcholine receptor, mitigates Alzheimer-associated phenotypes by inhibiting Aβ deposition and reactive astrogliosis.

International Journal of Biological Macromolecules
Alzheimer's disease (AD) is the most common form of dementia in older adults. Neuritic plaques and reactive astrogliosis are neuropathological hallmarks of AD.
Song Yue   +12 more
semanticscholar   +1 more source

Identification of key determinants in α subunit for α-conotoxin [D1G, ΔQ14]LvIC selectively targeting rat α6/α3β4 nicotinic acetylcholine receptor.

Neuropharmacology
nAChRs containing α6 subunit (α6* nAChRs) are identified as being involved in Parkinson's disease, dyskinesia, drug addiction, and other disorders. Among these, α6β4 nAChR is recognized as a highly promising target for the development of non-opioid ...
Baixue An   +7 more
semanticscholar   +1 more source

Site-specific post-translational modifications regulate the binding affinity of Conus amadis α-conotoxin Am2005 to Ac-AChBP.

Journal of Biomolecular Structure and Dynamics
Post-translational modifications (PTMs) play a pivotal role in diversifying the structure and function of peptide toxins from marine cone snails, which have proven applications in the treatment of neuropathic pain.
Shweta Dhannura   +6 more
semanticscholar   +1 more source

α-conotoxin TxID and its mutants targeting α3β4 nAChR subtype

Toxicon, 2019
Dongting Zhangsun   +10 more
semanticscholar   +1 more source

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