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Hampoelz, B.

Publications and source records attributed to Hampoelz, B..

3 recordsLinked to original sources

The small GTPase Ran defines Nuclear Pore Complex asymmetry

Nuclear pore complexes (NPCs) bridge across the nuclear envelope and mediate nucleocytoplasmic exchange. They consist of hundreds of nucleoporin building blocks and exemplify the structural complexity of macromolecular assemblies. To ensure transport directionality, different nucleoporin complexes are attached to the cytosolic and nuclear face of the NPC. How those asymmetric structures are faithfully assembled onto the symmetric scaffold architecture that exposes the same interaction surfaces to either side, remained enigmatic. Here we combine cryo-electron tomography, subtomogram averaging, and template matching with live cell imaging to address this question in budding yeast and Drosophila melanogaster. We genetically induce ectopic nuclear pores and show that pores outside the nuclear envelope are symmetric. We furthermore demonstrate that the peripheral NPC configuration depends on the nucleotide state of the small GTPase Ran. Our findings indicate that the nuclear transport system is self-regulatory, namely the same molecular mechanism controls both transport and transport channel composition.

cell biology↗

In-cell structure and snapshots of copia retrotransposons in intact tissue by cryo-electron tomography

Long terminal repeat (LTR) retrotransposons belong to the transposable elements (TE), autonomously replicating genetic elements that integrate into the hosts genome. LTR retrotransposons represent a major component of genomes across the tree of life; some derived sequences have even been domesticated by the host to perform cellular functions in essential processes such as development. Among animals, Drosophila melanogaster serves as an important model organism for TE research, harboring several LTR retrotransposons, including the Ty1-copia family, which is evolutionarily related to retroviruses and forms virus-like particles (VLPs). The architectural organization of copia VLPs in situ has remained unknown. In this study, we use cryo-FIB milling and lift-out approaches to visualize copia VLPs in isolated ovarian cells and intact egg chambers and resolve the in situ copia capsid structure to 7.7 [A] resolution by cryo-ET. While cytosolic copia VLPs vary in size, nuclear VLPs are homogenous and form densely packed clusters, supporting a model in which nuclear import acts as a size selector. By analyzing flies deficient in the TE-suppressing PIWI-piRNA pathway, we observe a change in copia localization from cytosolic to nuclear during spermatogenesis in testes. Our findings provide insights into the cellular structural biology of an active LTR retrotransposon and shed light on the replication cycle of copia in the context of host gametogenesis.

biophysics↗

A Modular Platform for Streamlining Automated Cryo-FIB Workflows

Lamella micromachining by focused ion beam milling at cryogenic temperature (cryo-FIB) has matured into a preparation method widely used for cellular cryo-electron tomography. Due to the limited ablation rates of low Ga+ ion beam currents required to maintain the structural integrity of vitreous specimens, current preparation protocols are time-consuming and labor intensive. The improved stability of new generation cryo-FIB instruments now enables automated operations. Here, we present an open-source software tool, SerialFIB, for creating automated and customizable cryo-FIB preparation protocols. The software encompasses a graphical user interface for easy execution of routine lamellae preparations, a scripting module compatible with available python packages, and interfaces with 3-dimensional correlative light and electron microscopy (CLEM) tools. The software enables the streamlining of advanced cryo-FIB protocols such as multi-modal imaging, CLEM guided preparation and in situ lamella lift-out procedures. Our software therefore provides a foundation for further development of advanced cryogenic imaging and sample preparation protocols.

biophysics↗