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超分辨率光学显微镜揭示了光激活登革病毒蛋白(Dendra2-NS2B)在内质网中的积累。

Super-resolution optical microscopy reveals accumulation of photoactivable dengue protein (Dendra2-NS2B) in the endoplasmic reticulum.

作者信息

Aravinth S, Varghese Jiby Mary, Pant Neeraj, Mondal Partha Pratim

机构信息

Department of Instrumentation and Applied Physics, Indian Institute of Science, Bangalore, 560012, India.

Centre for Cryogenic Technology, Indian Institute of Science, Bangalore, 560012, India.

出版信息

Sci Rep. 2025 Mar 26;15(1):10358. doi: 10.1038/s41598-025-94135-6.

Abstract

The non-structural protein NS2B plays a critical role in the maturation of Dengue virus (DENV Type 2). The underlying mechanism and the role of NS2B are largely unknown due to the unavailability of its location of activity in the target organelle at single molecule level. This is largely due to the incapability of existing optical microscopes to resolve features beyond the diffraction limit of light ([Formula: see text]), which is limited to a few hundred nanometers. Existing microscopy techniques are at best useful for ensemble study and details at the single molecule level remain hidden. To enable single-molecule resolution, we investigated the role of NS2B protein in a cellular system using scanning single molecule localization microscopy (scanSMLM). Accordingly, a photoactivable plasmid (Dendra2-NS2B) containing the gene-of-interest (NS2B) was constructed and the same is used to transfect NIH3T3 cells. Both super-resolution and confocal imaging studies suggest the accumulation of NS2B proteins in endoplasmic reticulum (ER). Subsequently, single-molecule analysis is carried out, where a total of [Formula: see text] NS2B aggregates (both big and small) are noted with an area-spread of [Formula: see text], the molecular density of [Formula: see text], and an average of [Formula: see text] NS2B molecules per cluster. Moreover, the super-resolved volume image revealed NS2B clusters spreading across several planes with a few extending up to 5 planes ([Formula: see text] from the coverslip). In addition, the collective dynamics of NS2B proteins leading to the formation of clusters is evident from time-lapse super-resolved data that provides conclusive evidence of NS2B accumulation, 24 hrs post-transfection. The present study revealed the dynamics of NS2B single viral protein molecule, and its accumulation at ER that may ultimately lead to organelle-specific drug targeting and help to reduce the rate of dengue infection by disrupting the NS2B accumulates.

摘要

非结构蛋白NS2B在登革病毒(2型登革病毒)的成熟过程中起关键作用。由于无法在单分子水平上确定其在靶细胞器中的活性位置,NS2B的潜在机制和作用在很大程度上尚不清楚。这主要是由于现有的光学显微镜无法分辨超出光的衍射极限([公式:见正文])的特征,该极限限制在几百纳米。现有的显微镜技术充其量仅适用于整体研究,单分子水平的细节仍然隐藏。为了实现单分子分辨率,我们使用扫描单分子定位显微镜(scanSMLM)在细胞系统中研究了NS2B蛋白的作用。因此,构建了一个包含感兴趣基因(NS2B)的光活化质粒(Dendra2-NS2B),并将其用于转染NIH3T3细胞。超分辨率和共聚焦成像研究均表明NS2B蛋白在内质网(ER)中积累。随后,进行单分子分析,共记录到[公式:见正文]个NS2B聚集体(大小均有),面积分布为[公式:见正文],分子密度为[公式:见正文],每个簇平均有[公式:见正文]个NS2B分子。此外,超分辨体积图像显示NS2B簇分布在多个平面上,少数簇延伸至5个平面(距盖玻片[公式:见正文])。此外,延时超分辨数据显示了NS2B蛋白形成簇的集体动力学,这为转染后24小时NS2B的积累提供了确凿证据。本研究揭示了NS2B单个病毒蛋白分子的动力学及其在内质网中的积累,这最终可能导致细胞器特异性药物靶向,并通过破坏NS2B的积累来帮助降低登革热感染率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a750/11937263/9ca606b3a8aa/41598_2025_94135_Fig1_HTML.jpg

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