| Online-Ressource |
Verfasst von: | Petrich, Annett [VerfasserIn]  |
| Hwang, Gyu Min [VerfasserIn]  |
| La Rocca, Laetitia [VerfasserIn]  |
| Hassan, Mariam [VerfasserIn]  |
| Anders-Ößwein, Maria [VerfasserIn]  |
| Sonntag-Buck, Vera [VerfasserIn]  |
| Heuser, Anke-Mareil [VerfasserIn]  |
| Laketa, Vibor [VerfasserIn]  |
| Müller, Barbara [VerfasserIn]  |
| Kräusslich, Hans-Georg [VerfasserIn]  |
| Klaus, Severina [VerfasserIn]  |
Titel: | Expanding insights |
Titelzusatz: | harnessing expansion microscopy for super-resolution analysis of HIV-1-cell interactions |
Verf.angabe: | Annett Petrich, Gyu Min Hwang, Laetitia La Rocca, Mariam Hassan, Maria Anders-Össwein, Vera Sonntag-Buck, Anke-Mareil Heuser, Vibor Laketa, Barbara Müller, Hans-Georg Kräusslich and Severina Klaus |
E-Jahr: | 2024 |
Jahr: | 15 October 2024 |
Umfang: | 26 S. |
Illustrationen: | Illustrationen |
Fussnoten: | Gesehen am 24.03.2025 |
Titel Quelle: | Enthalten in: Viruses |
Ort Quelle: | Basel : MDPI, 2009 |
Jahr Quelle: | 2024 |
Band/Heft Quelle: | 16(2024), 10, Artikel-ID 1610, Seite 1-26 |
ISSN Quelle: | 1999-4915 |
Abstract: | Expansion microscopy has recently emerged as an alternative technique for achieving high-resolution imaging of biological structures. Improvements in resolution are achieved by physically expanding samples through embedding in a swellable hydrogel before microscopy. However, expansion microscopy has been rarely used in the field of virology. Here, we evaluate and characterize the ultrastructure expansion microscopy (U-ExM) protocol, which facilitates approximately four-fold sample expansion, enabling the visualization of different post-entry stages of the HIV-1 life cycle, focusing on nuclear events. Our findings demonstrate that U-ExM provides robust sample expansion and preservation across different cell types, including cell-culture-adapted and primary CD4+ T-cells as well as monocyte-derived macrophages, which are known HIV-1 reservoirs. Notably, cellular targets such as nuclear bodies and the chromatin landscape remain well preserved after expansion, allowing for detailed investigation of HIV-1-cell interactions at high resolution. Our data indicate that morphologically distinct HIV-1 capsid assemblies can be differentiated within the nuclei of infected cells and that U-ExM enables detection of targets that are masked in commonly used immunofluorescence protocols. In conclusion, we advocate for U-ExM as a valuable new tool for studying virus-host interactions with enhanced spatial resolution. |
DOI: | doi:10.3390/v16101610 |
URL: | Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.
kostenfrei: Volltext: https://doi.org/10.3390/v16101610 |
| kostenfrei: Volltext: https://www.mdpi.com/1999-4915/16/10/1610 |
| DOI: https://doi.org/10.3390/v16101610 |
Datenträger: | Online-Ressource |
Sprache: | eng |
Sach-SW: | expansion microscopy |
| HIV-1 |
| HIV-1 capsid |
| HIV-1 nuclear import |
| HIV-1 post-entry |
| super-resolution microscopy |
| ultrastructure expansion microscopy |
| virus-host interaction |
K10plus-PPN: | 1920388125 |
Verknüpfungen: | → Zeitschrift |
Expanding insights / Petrich, Annett [VerfasserIn]; 15 October 2024 (Online-Ressource)