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抗疟活性:海洋异腈抑制血红素结晶的首个证据。

Antiplasmodial activity: the first proof of inhibition of heme crystallization by marine isonitriles.

作者信息

Young Ryan M, Adendorff Matthew R, Wright Anthony D, Davies-Coleman Michael T

机构信息

Department of Chemistry, Rhodes University, Grahamstown, South Africa.

DKI-College of Pharmacy, University of Hawaii at Hilo, Hilo, USA.

出版信息

Eur J Med Chem. 2015 Mar 26;93:373-80. doi: 10.1016/j.ejmech.2015.02.011. Epub 2015 Feb 9.

Abstract

Over a decade ago Wright et al., proposed a putative antiplasmodial mechanism of action for marine isonitriles (1, and 3-6) and isothiocyanate (2) that involved interference in heme detoxification by Plasmodium falciparum thus inhibiting the growth of the parasite. In the current paper we describe the successful down scaling of Egan's β-hematin inhibition assay for analyses of small quantities of marine natural products as potential β-hematin inhibitors. The modified assay revealed for the first time that the most active antiplasmodial marine isonitrile 4 (IC50 13 nM) totally inhibited β-hematin crystallization while 5 (IC50 31 nM) and 6 (IC50 81 nM) showed inhibition at lower levels. A cursory ab initio molecular dynamics investigation into the relative stabilities of bonded complexes between isocyanate, isothiocyanate and isonitrile groups with the iron center of heme supported our findings that these marine metabolites do indeed interfere with biocrystallization of heme.

摘要

十多年前,赖特等人提出了海洋异腈(1以及3 - 6)和异硫氰酸酯(2)可能的抗疟作用机制,该机制涉及干扰恶性疟原虫的血红素解毒过程,从而抑制寄生虫的生长。在本文中,我们描述了成功缩小伊根的β - 血红素抑制试验规模,用于分析少量海洋天然产物作为潜在的β - 血红素抑制剂。改进后的试验首次表明,活性最强的抗疟海洋异腈4(IC50为13 nM)完全抑制了β - 血红素结晶,而5(IC50为31 nM)和6(IC50为81 nM)则表现出较低水平的抑制作用。对异氰酸酯、异硫氰酸酯和异腈基团与血红素铁中心之间键合复合物的相对稳定性进行的初步从头算分子动力学研究支持了我们的发现,即这些海洋代谢产物确实会干扰血红素的生物结晶。

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