• Refine Query
  • Source
  • Publication year
  • to
  • Language
  • 1
  • Tagged with
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
1

Cell Migration is Regulated by Mitochondria and Endoplasmic Reticulum Morphology.

Daniel, Redaet 11 June 2020 (has links)
Cell migration is essential for homeostasis and the development of metastases. We hypothesize that cell migration is regulated by mitochondria and endoplasmic reticulum morphology. Using live cell microscopy, we found that mitochondria specifically migrate into the biochemically dense leading edge of the cell interacting with focal adhesions as well. At the leading edge the mitochondria are visibly shorter and less tubular than the perinuclear area. This is related to the elevated levels of fission events per minute in the leading edge and elevated levels of fusion events per minute in the trailing edge. We observe that mitochondria migrate along microtubules and simultaneously interact with the ER. When the ER is sheet-like the mitochondria are longer and tubular and when the ER is tubular the mitochondria are shorter and punctate. This change in ER and mitochondria morphology changes the cell’s ability to migrate. CLIMP63 cells have more sporadic turns, take longer to make turns, have shorter distances travelled and shorter displacements. To determine whether mitochondria dynamics play a role we examined these cell migration parameters in the presence of OPA1 and Drp1. This allowed us to conclude that the ER morphology is responsible for the distance and displacement the cell travels while the mitochondria is responsible for the angles the cell turns. When the ER is sheet-like the cells will be travel shorter total distances and displacements and when the cell has longer mitochondria it will be sporadic turns and take longer to make these turns.
2

The molecular basis for ER tubule formation

Brady, Jacob Peter January 2015 (has links)
Integral membrane proteins of the DP1 and reticulon families are responsible for maintaining the high membrane curvature required for both smooth ER tubules and the edges of ER sheets. Mutations in these proteins lead to motor neurone diseases such as hereditary spastic paraplegia. Reticulon/DP1 proteins contain Reticulon Homology Domains (RHD) that have unusually long (≈30 aa) hydrophobic segments and are proposed to adopt intramembrane helical hairpins that stabilise membrane curvature. I have uncovered the secondary structure and dynamics of the DP1 protein Yop1p and identified a C-terminal conserved amphipathic helix that on its own interacts strongly with negatively charged membranes and is necessary for membrane tubule formation. Analyses of DP1 and reticulon family members indicate that most, if not all, contain C-terminal sequences capable of forming amphipathic helices. Together, these results indicate that amphipathic helices play a previously unrecognised role in RHD membrane curvature stabilisation. This work paves the way towards full structure determination of Yop1p by solution state NMR and marks the first high structural resolution study on an RHD protein.

Page generated in 0.0376 seconds