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溶血磷脂的合成。

Synthesis of lysophospholipids.

机构信息

Dipartimento di Chimica, Materiali ed Ingegneria Chimica Giulio Natta, Politecnico di Milano, Via Mancinelli 7, 20131 Milano, Italy. paola.d'

出版信息

Molecules. 2010 Mar 8;15(3):1354-77. doi: 10.3390/molecules15031354.

Abstract

New synthetic methods for the preparation of biologically active phospholipids and lysophospholipids (LPLs) are very important in solving problems of membrane-chemistry and biochemistry. Traditionally considered just as second-messenger molecules regulating intracellular signalling pathways, LPLs have recently shown to be involved in many physiological and pathological processes such as inflammation, reproduction, angiogenesis, tumorogenesis, atherosclerosis and nervous system regulation. Elucidation of the mechanistic details involved in the enzymological, cell-biological and membrane-biophysical roles of LPLs relies obviously on the availability of structurally diverse compounds. A variety of chemical and enzymatic routes have been reported in the literature for the synthesis of LPLs: the enzymatic transformation of natural glycerophospholipids (GPLs) using regiospecific enzymes such as phospholipases A1 (PLA1), A2 (PLA2) phospholipase D (PLD) and different lipases, the coupling of enzymatic processes with chemical transformations, the complete chemical synthesis of LPLs starting from glycerol or derivatives. In this review, chemo-enzymatic procedures leading to 1- and 2-LPLs will be described.

摘要

新的合成方法,用于制备具有生物活性的磷脂和溶血磷脂(LPL)在解决膜化学和生物化学问题方面非常重要。传统上,LPL 仅被认为是调节细胞内信号通路的第二信使分子,但最近已显示其参与许多生理和病理过程,如炎症、生殖、血管生成、肿瘤发生、动脉粥样硬化和神经系统调节。阐明 LPL 在酶学、细胞生物学和膜生物物理学作用中的机制细节显然依赖于具有结构多样性的化合物的可用性。文献中已经报道了多种用于合成 LPL 的化学和酶法途径:使用磷脂酶 A1(PLA1)、A2(PLA2)、磷脂酶 D(PLD)和不同脂肪酶等区域特异性酶对天然甘油磷脂(GPL)的酶促转化、酶促过程与化学转化的偶联、从甘油或衍生物开始的 LPL 的完全化学合成。在这篇综述中,将描述导致 1-和 2-LPL 的化学-酶促程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f74e/6257299/131ae730c2c5/molecules-15-01354-g001.jpg

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