Abstract
This paper discusses the properties of the three most specific ligands found for the extracellular faces of M1, M2 and M4 muscarinic receptors (m1-toxin1, m2-toxin and m4-toxin, respectively). The primary goal of this paper is to show the known and potential usefulness of these toxins and their biotinylated, radioactive, fluorescent and mutated derivatives.
MeSH terms
-
Amino Acid Sequence
-
Animals
-
Binding Sites
-
Elapid Venoms / chemistry
-
Elapid Venoms / metabolism*
-
Elapid Venoms / pharmacology
-
Elapidae / metabolism
-
Humans
-
Molecular Sequence Data
-
Muscarinic Antagonists / chemistry
-
Muscarinic Antagonists / metabolism
-
Muscarinic Antagonists / pharmacology
-
Neurotoxins / chemistry
-
Neurotoxins / metabolism
-
Neurotoxins / pharmacology
-
Protein Binding
-
Receptor, Muscarinic M1
-
Receptor, Muscarinic M2
-
Receptor, Muscarinic M4
-
Receptors, Muscarinic / metabolism*
-
Sequence Alignment
Substances
-
Elapid Venoms
-
Muscarinic Antagonists
-
Neurotoxins
-
Receptor, Muscarinic M1
-
Receptor, Muscarinic M2
-
Receptor, Muscarinic M4
-
Receptors, Muscarinic
-
m1-toxin
-
m2-toxin
-
muscarinic toxin MT4