Kryukova E V, Ivanov I A, Lebedev D S, Spirova E N, Senko D A, Egorova N S, Kasheverov I E, Tsetlin V I
Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, Moscow, 117997, Russia.
Sechenov First Moscow State Medical University, Ministry of Healthcare of the Russian Federation, Moscow, 119992, Russia.
Dokl Biochem Biophys. 2018 Nov;483(1):313-315. doi: 10.1134/S1607672918060017. Epub 2019 Jan 3.
Arginine-containing peptides R3, R8, and R16 were obtained by solid-phase peptide synthesis, and their binding to nicotinic acetylcholine receptors (nAChRs) of muscle and neuronal (α7) types was studied by competitive radioligand assay with the use of I-α-bungarotoxin. The resulting peptides exhibited a significantly greater binding activity with respect to the muscle-type nAChRs than to the α7 receptor. Thus, we have discovered a new class of nAChR ligands. The affinity of the synthesized oligoarginines for nAChR depended on the number of amino acid residues in the chain. The highest affinity was exhibited by the R16 peptide, which contained 16 arginine residues.
含精氨酸的肽R3、R8和R16通过固相肽合成获得,并使用I-α-银环蛇毒素通过竞争性放射性配体测定法研究了它们与肌肉型和神经元型(α7)烟碱型乙酰胆碱受体(nAChRs)的结合。所得肽对肌肉型nAChRs的结合活性比对α7受体的结合活性显著更高。因此,我们发现了一类新的nAChR配体。合成的寡聚精氨酸对nAChR的亲和力取决于链中氨基酸残基的数量。含16个精氨酸残基的R16肽表现出最高的亲和力。