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胆固醇衍生物通过结合胞质亚基中的CARC和CRAC基序来调节腺苷酸环化酶7的活性。

Cholesterol Derivatives Regulate Adenylyl Cyclase 7 Activity by Binding CARC and CRAC Motifs in the Cytosolic Subunits.

作者信息

Jaroušek Radim, Dad'ová Petra, Litvinchuk Alexandra, Dobler Leticia, Kubala Lukáš

机构信息

Department of Experimental Biology, Faculty of Science, Masaryk University, Kotlářská 2, 602 00 Brno, Czech Republic.

Department of Biophysics of the Immune System, Institute of Biophysics, Czech Academy of Sciences, Královopolská 135, 612 00 Brno, Czech Republic.

出版信息

ACS Omega. 2025 Aug 14;10(33):37039-37052. doi: 10.1021/acsomega.5c00741. eCollection 2025 Aug 26.

Abstract

Transmembrane adenylyl cyclases (tmACs; ACs) are enzymes that synthesize cyclic AMP (cAMP), which is a key molecule in cellular signaling. Disruptions in AC activity can lead to long-term shifts in cAMP levels associated with various pathologies. In our study, we analyzed AC primary sequences and identified cholesterol-binding CARC and CRAC motifs located in conserved cytosolic regions, a surprising finding for motifs that are typically membrane-associated. Focusing on AC7, we mapped these motifs within its predicted structure and performed docking studies with cholesterol derivatives (hydrocortisone, dexamethasone, and 25-hydroxycholesterol). Our results showed that these molecules predominantly bind to the forskolin (FSK) binding site, which contains two CARC motifs. Using membranes overexpressing AC7, we observed that all three derivatives significantly decreased FSK-mediated AC7 activity by up to 55%. This suggests that cholesterol derivatives might interact with CARC and CRAC motifs to regulate AC7 function and underscore the potential of cholesterol derivatives as natural modulators as well as provide a compelling basis for future exploration of cholesterol derivatives as possible therapeutic regulators of AC7.

摘要

跨膜腺苷酸环化酶(tmACs;ACs)是合成环磷酸腺苷(cAMP)的酶,cAMP是细胞信号传导中的关键分子。AC活性的破坏会导致与各种病理相关的cAMP水平长期变化。在我们的研究中,我们分析了AC的一级序列,并在保守的胞质区域中鉴定出胆固醇结合基序CARC和CRAC,这对于通常与膜相关的基序来说是一个惊人的发现。以AC7为重点,我们在其预测结构中定位了这些基序,并与胆固醇衍生物(氢化可的松、地塞米松和25-羟基胆固醇)进行了对接研究。我们的结果表明,这些分子主要与福斯可林(FSK)结合位点结合,该位点包含两个CARC基序。使用过表达AC7的膜,我们观察到所有三种衍生物均使FSK介导的AC7活性显著降低,降幅高达55%。这表明胆固醇衍生物可能与CARC和CRAC基序相互作用以调节AC7功能,并强调了胆固醇衍生物作为天然调节剂的潜力,同时也为未来将胆固醇衍生物作为AC7可能的治疗调节剂进行探索提供了令人信服的依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e9ff/12391971/5c1e92a7cc5c/ao5c00741_0001.jpg

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