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Herpes simplex virus 1 (HSV-1) remodels nuclear membranes during virus egress. Although the UL31 and UL34 proteins control nucleocapsid transit in infected cells, the molecular interactions required for their function are unclear. Here we report that the ␥ 1 34.5 gene product of HSV-1 facilitates nucleocapsid release to the cytoplasm through bridging the UL31/UL34 complex, cellular p32, and protein kinase C. Unlike wild-type virus, an HSV mutant devoid of ␥ 1 34.5 or its amino terminus is crippled for viral growth and release. This is attributable to a defect in virus nuclear egress. In infected cells, wild-type virus recruits protein kinase C to the nuclear membrane and triggers its activation, whereas the ␥ 1 34.5 mutants fail to exert such an effect. Accordingly, the ␥ 1 34.5 mutants are unable to induce phosphorylation and reorganization of lamin A/C. When expressed in host cells ␥ 1 34.5 targets p32 and protein kinase C. Meanwhile, it communicates with the UL31/UL34 complex through UL31. Deletion of the amino terminus from ␥ 1 34.5 disrupts its activity. These results suggest that disintegration of the nuclear lamina mediated by ␥ 1 34.5 promotes HSV replication. IMPORTANCEHSV nuclear egress is a key step that determines the outcome of viral infection. While the nuclear egress complex mediates capsid transit across the nuclear membrane, the regulatory components are not clearly defined in virus-infected cells. We report that the ␥ 1 34.5 gene product, a virulence factor of HSV-1, facilitates nuclear egress cooperatively with cellular p32, protein kinase C, and the nuclear egress complex. This work highlights a viral mechanism that may contribute to the pathogenesis of HSV infection. Herpes simplex virus 1 (HSV-1) replicates and packages its DNA in the cell nucleus. Once assembled, the nucleocapsids traverse the nucleoplasm and cross the nuclear lamina. The capsids bud through the nuclear membranes in a two-step process called envelopment and de-envelopment (1). In this process, the nuclear egress complex, consisting of UL31 and UL34, mediates vesiculation of the inner nuclear membrane and results in enveloped virions in the perinuclear space. Primary virions fuse with the outer nuclear membrane, which releases the capsids to the cytoplasm for further maturation (2). Accumulating evidence suggests that additional proteins, including Us3, ICP22, UL47, gB, and gH, coordinate with the UL31/34 complex to facilitate nuclear egress in infected cells (3-6).The nuclear lamina is a dense meshwork underlying the inner nuclear membrane (7). It is composed primarily of type V intermediate filament proteins, lamin A/C and lamin B. Besides providing structural support to the nucleus, the nuclear lamina potentially presents a barrier to the transit of virus capsids. A number of studies suggest that herpesviruses alter the nuclear lamina to promote nuclear egress (8-11). For example, HSV-1 activates protein kinase C (PKC) isoforms and induces phosphorylation of lamin B, which is dependent on the UL31/UL34 complex (1...

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Lipidomics is a significant way to understand the structural and functional roles that lipids play in biological systems. Although many mass spectrometry (MS)-based lipidomics strategies have recently achieve remarkable results, in vivo, in situ, and microscale lipidomics for small biological organisms and cells have not yet been obtained. In this article, we report a novel lipidomics methodology for in vivo, in situ, and microscale investigation of small biological organisms and cells using biocompatible surface-coated probe nanoelectrospray ionization mass spectrometry (BSCP-nanoESI-MS). A novel biocompatible surface-coated solid-phase microextration (SPME) probe is prepared, which possesses a probe-end diameter of less than 5 μm and shows excellent enrichment capacity toward lipid species. In vivo extraction of living biological organisms (e.g., zebrafishes), in situ sampling a precise position of small organisms (e.g., Daphnia magna), and even microscale analysis of single eukaryotic cells (e.g., HepG2) are easily achieved by the SPME probe. After extraction, the loaded SPME probe is directly applied for nanoESI-MS analysis, and a high-resolution mass spectrometer is employed for recording spectra and identifying lipid species. Compared with the conventional direct infusion shotgun MS lipidomics, our proposed methodology shows a similar result of lipid profiles but with simpler sample pretreatment, less sample consumption, and shorter analytical times. Lipidomics of zebrafish, Daphnia magna, and HepG2 cell populations were investigated by our proposed BSCP-nanoESI-MS methodology, and abundant lipid compositions were detected and identified and biomarkers were obtained via multivariate statistical analysis.

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Lipids are important structural components of biological systems, and lipid CC locations play important roles in their biophysical and biochemical properties. Rapid, in vivo, in situ, and microscale lipidomics investigation (including precise identification of lipid CC locations and isomers) of biological specimen has great potential for clinical diagnosis, biological studies, and biomarker discovery. Here we report a novel lipidomics methodology by coupling Paternò-Büchi (PB) reaction with surface-coated probe nanoelectrospray ionization mass spectrometry (SCP-nanoESI-MS) for in vivo, in situ, and microscale analysis of lipid species and CC location isomers in complex biological tissues. The proposed SCP-PB-nanoESI-MS method was performed by application of a biocompatible solid-phase microextraction (SPME) probe for in vivo, in situ, and microscale sampling and extraction of lipids from biological tissues, and then some spray solvent containing PB reagent was applied to desorb lipid species enriched on SPME probe within a nanospray tip. Subsequently, ultraviolet irradiation was employed to initiate PB reaction for unsaturated lipids within the nanospray tip. After that, a high voltage was applied on the SPME probe to induce nanoESI for MS analysis under ambient and open-air conditions, and collision-induced dissociation was performed to the PB reaction product ions for determination of lipid CC locations and isomers. By using our proposed SCP-BP-nanoESI-MS method, microscale investigation of lipid compositions and CC location isomers for lipid droplet of Perilla seed and human intestinal tissue were successfully achieved, and in vivo analysis of lipid species and CC locations for zebrafish was accomplished.