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<title>TDX test</title>
<link href="http://hdl.handle.net/123456789/38085" rel="alternate"/>
<subtitle/>
<id>http://hdl.handle.net/123456789/38085</id>
<updated>2026-05-27T05:26:31Z</updated>
<dc:date>2026-05-27T05:26:31Z</dc:date>
<entry>
<title>Resolving the continuous high-order organization of the exocyst during vesicle tethering</title>
<link href="http://hdl.handle.net/123456789/38086" rel="alternate"/>
<author>
<name>Ortiz Giron, Jhoan Sebastian</name>
</author>
<id>http://hdl.handle.net/123456789/38086</id>
<updated>2025-10-28T14:17:33Z</updated>
<published>2025-09-22T00:00:00Z</published>
<summary type="text">Resolving the continuous high-order organization of the exocyst during vesicle tethering
Ortiz Giron, Jhoan Sebastian
Constitutive exocytosis is an essential and highly-conserved trafficking pathway for the delivering of cargo  to the plasma membrane and the extracellular space. During this pathway, cargo-loaded vesicles are tethered to the plasma membrane by the exocyst, an heterodiramic complex, prior the vesicle fusion.  Despite exocyst-mediated vesicle tethering represents a crucial stage, how multiple exocysts organize in space and time remains poorly understood. Here, we employed an integrative approach to unveil the dynamic architecture of exocyst-mediated vesicle tethering. To achieve this goal, we developed a computational workflow for the analysis of datasets from live-cell imaging, super-resolution microscopy and correlative cryo-electron tomography. We demonstrated that the exocyst high-order structure consists on seven exocyst, on average, assembled into in ring-like shapes. The radius of those rings expand from 18 to 38 nm following a saturated-exponential function defined by a characteristic time of 3.1 s.
</summary>
<dc:date>2025-09-22T00:00:00Z</dc:date>
</entry>
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