感染与糖粒--宿主反应的新见解。

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2024-08-09 Epub Date: 2024-07-11 DOI:10.1021/acsinfecdis.4c00315
F Ifthiha Mohideen, Lara K Mahal
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引用次数: 0

摘要

糖基化在导致感染的宿主-病原体相互作用中起着关键作用。然而,我们对糖基化在应对感染时的动态性质及其在调节宿主免疫力方面的功能仍然知之甚少。许多参与免疫防御的宿主蛋白质都是糖蛋白。此外,先天性免疫系统也能识别糖蛋白。蛋白质的糖型会影响蛋白水解稳定性、受体相互作用、血清半衰期和其他方面。新的尖端化学生物学工具正在揭示感染与宿主糖蛋白之间的相互作用。在这篇综述中,我们将重点介绍有关宿主蛋白质动态糖基化在先天性和适应性免疫途径中应对感染的重要性的新研究成果。其中包括最近关于粘蛋白、补体成分和抗体的糖基化改变的发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Infection and the Glycome─New Insights into Host Response.

Infection and the Glycome─New Insights into Host Response.

Glycans play critical roles in the host-pathogen interactions leading to infection. However, we still understand very little about the dynamic nature of glycosylation in response to infection and its function in modulating host immunity. Many of the host proteins involved in immune defense are glycoproteins. Furthermore, the innate immune system recognizes glycans. The glycoform of a protein can impact proteolytic stability, receptor interactions, serum half-life, and other aspects. New, cutting-edge chemical biology tools are shedding light on the interplay between infection and the host glycome. In this review, we highlight new work on the importance of dynamic glycosylation of host proteins in the innate and adaptive immune pathways in response to infection. These include recent findings on altered glycoprofiles of mucins, complement components, and antibodies.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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