State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Beijing, 100191, China.
Chembiochem. 2018 Jul 4;19(13):1444-1451. doi: 10.1002/cbic.201800133. Epub 2018 May 22.
Cyclic adenosine diphosphate ribose (cADPR) is an endogenous Ca mobilizer involved in diverse cellular processes. Mimics of cADPR play a crucial role in investigating the molecular mechanism(s) of cADPR-mediated signaling. Here, compound 3, a mimic of cADPR in which a neutral triazole moiety and an ether linkage were introduced to substitute the pyrophosphate and "northern" ribose components, respectively, was synthesized for the first time. The pharmacological activities in Jurkat cells indicated that this mimic is capable of penetrating plasma membrane and inciting Ca release from the endoplasmic reticulum (ER) through the action of ryanodine receptors (RyRs) and triggering Ca influx. Furthermore, a uridine moiety was introduced in place of adenine and the new cADPR mimics 4 and 5 were synthesized. The results of biological investigation showed that these mimics also targeted RyRs and retained moderate Ca agonistic activities. The results indicated that the neutral cADPR mimics had the same targets for inducing Ca signaling.
环腺苷二磷酸核糖(cADPR)是一种内源性 Ca 动员剂,参与多种细胞过程。cADPR 的模拟物在研究 cADPR 介导的信号转导的分子机制方面起着至关重要的作用。在这里,首次合成了 cADPR 的模拟物 3,其中用中性三唑取代了焦磷酸和“北”核糖部分,并引入了醚键。在 Jurkat 细胞中的药理学活性表明,这种模拟物能够穿透质膜,并通过肌醇 1,4,5-三磷酸受体(RyRs)的作用从内质网(ER)中引发 Ca 释放,并触发 Ca 内流。此外,用尿嘧啶取代了腺嘌呤,并合成了新的 cADPR 模拟物 4 和 5。生物学研究的结果表明,这些模拟物也靶向 RyRs 并保留了中等的 Ca 激动活性。结果表明,中性 cADPR 模拟物具有相同的诱导 Ca 信号的靶标。