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来自海洋的信号:脂质A的结构特性以及来自……的弱免疫刺激性脂多糖

Signals from the sea: the structural peculiarity of lipid A and weak immunostimulatory lipopolysaccharide from .

作者信息

De Chiara Stefania, Olmeo Francesca, Andretta Emanuela, De Simone Carone Luca, Mercogliano Marcello, Belova Vlada S, Romanenko Lyudmila A, Kokoulin Maxim S, Silipo Alba, Molinaro Antonio, Di Lorenzo Flaviana

机构信息

Department of Chemical Sciences, University of Naples Federico II via Cinthia, 4 80126 Naples Italy

CEINGE-Biotecnologie Avanzate Franco Salvatore s.c.ar.l. Via G. Salvatore, 436 80131 Naples Italy.

出版信息

RSC Chem Biol. 2025 Jul 7. doi: 10.1039/d5cb00134j.

Abstract

Lipopolysaccharides (LPSs) isolated from marine bacteria represent a valuable resource for biomedical innovation. Here, we report the first structural elucidation of the lipid A moiety and a preliminary immunological assessment of the full LPS from the marine Gram-negative KMM 9513. Using MALDI-TOF mass spectrometry (MS) and tandem MS, we show that the lipid A from KMM 9513 exhibits a heterogeneous architecture, composed of - and -phosphorylated tetra- and penta-acylated species with variations in the acyl chain length, saturation, branching, and positional isomerism. Functionally, the full LPS was found to be immunologically silent toward TLR4-mediated NF-κB activation in HEK-Blue™ hTLR4 cells and triggered only modest, dose-dependent responses in differentiated human THP-1 macrophages. Strikingly, the LPS was able to antagonize LPS-induced TLR4 activation, even at low doses. Overall, this study uncovers a structurally and functionally atypical marine LPS with a dual profile, inactive towards TLR4 yet capable of modulating LPS-induced signaling. These findings offer a promising basis to consider LPS as a source of structural inspiration for the design of synthetic derivatives with controlled immunological properties.

摘要

从海洋细菌中分离出的脂多糖(LPS)是生物医学创新的宝贵资源。在此,我们报告了海洋革兰氏阴性菌KMM 9513的脂质A部分的首次结构解析以及完整LPS的初步免疫学评估。使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)和串联质谱,我们表明KMM 9513的脂质A呈现出异质结构,由α-和β-磷酸化的四酰化和五酰化物种组成,酰基链长度、饱和度、分支和位置异构存在差异。在功能上,发现完整的LPS对HEK-Blue™ hTLR4细胞中TLR4介导的NF-κB激活在免疫上无活性,并且在分化的人THP-1巨噬细胞中仅引发适度的剂量依赖性反应。引人注目的是,该LPS即使在低剂量下也能够拮抗LPS诱导的TLR4激活。总体而言,本研究揭示了一种结构和功能上非典型的海洋LPS,具有双重特性,对TLR4无活性但能够调节LPS诱导的信号传导。这些发现为将该LPS视为设计具有可控免疫特性的合成衍生物的结构灵感来源提供了有前景的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a813/12394828/18dcbab77f52/d5cb00134j-f1.jpg

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