Anti-infective nanodisc
dc.rights.license | CC-BY-NC-ND | |
dc.contributor.advisor | Vries, Robert de | |
dc.contributor.author | Falier, Sanne van | |
dc.date.accessioned | 2024-02-23T01:00:58Z | |
dc.date.available | 2024-02-23T01:00:58Z | |
dc.date.issued | 2024 | |
dc.identifier.uri | https://studenttheses.uu.nl/handle/20.500.12932/46054 | |
dc.description.abstract | Influenza virus, a significant public health concern, continuously mutates, leading to challenges in vaccine and antiviral drug development. While clinical antiviral drugs primarily target specific viral proteins, nanodiscs have emerged as a novel therapeutic approach. Nanodiscs, composed of phospholipid bilayers and amphipathic proteins, mimic cell membranes, providing a controlled, biologically relevant environment for the study of membrane proteins. Their ability to disrupt viral infection in several ways has been studied. By incorporating nanodiscs containing host cell receptors, they can perforate the viral envelope, rendering the virus unable to replicate. Another inhibitory mechanism involves nanodiscs with antibodies, blocking their viral receptors. Nanodiscs offer advantages including improved stability, specific targeting, and broad biocompatibility. Nanodiscs represent a promising avenue for combating influenza and other enveloped viral infections. | |
dc.description.sponsorship | Utrecht University | |
dc.language.iso | EN | |
dc.subject | A review of the possibilities of a nanodisc against Influenza A virus infection. A nanodisc mimics the bilayer of the cell membrane creating different therapeutic options. When a receptor recognized by the virus is inserted inside the nanodisc, the disc can perforate the viral membrane or elicit an immune response. | |
dc.title | Anti-infective nanodisc | |
dc.type.content | Master Thesis | |
dc.rights.accessrights | Open Access | |
dc.subject.keywords | Nanodisc; Inlfuenza A; anti-infective; nanoperforator; antibody-nanodisc complex; membrane disrupting; di-disc; therapeutic | |
dc.subject.courseuu | Molecular and Cellular Life Sciences | |
dc.thesis.id | 28393 |