Evidence map›Paper›PMID 39416124›Full record

ArticlebioRxiv : the preprint server for biology2024

ExoSloNano: Multi-Modal Nanogold Tags for identification of Macromolecules in Live Cells & Cryo-Electron Tomograms.

Lindsey N Young, Alice Sherrard, Huabin Zhou, Farhaz Shaikh, Joshua Hutchings, Margot Riggi, Michael K Rosen, Antonio J Giraldez, Elizabeth Villa

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Lindsey N YoungSchool of Biological Sciences, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0003-3494-8302
Alice SherrardYale University, New Haven, CT, USA.ORCID 0000-0003-1220-4492
Huabin ZhouUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-7788-0806
Farhaz ShaikhSchool of Biological Sciences, University of California San Diego, La Jolla, CA, USA.ORCID 0009-0002-0452-5675
Joshua HutchingsSchool of Biological Sciences, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0001-6841-8583
Margot RiggiMax Planck Institute for Biochemistry, Martinsried, Germany.ORCID 0000-0002-8930-5331
Michael K RosenUniversity of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID 0000-0002-0775-7917
Antonio J GiraldezYale University, New Haven, CT, USA.ORCID 0000-0002-6823-137X
Elizabeth VillaSchool of Biological Sciences, University of California San Diego, La Jolla, CA, USA.ORCID 0000-0003-4677-9809

Funding

ChimeraX -- Next Generation Visualization and Analysis Software for Multiscale ModelingR01GM129325 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FERRIN, THOMAS E · 2018 to 2025
$5.2M
Opening Windows into the Cell: Revealing the Molecular Architecture of the Nuclear PeripheryDP2GM123494 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VILLA, ELIZABETH · 2016 to 2019
$2.5M
Cell Organization Through Phase Separation: Mechanisms, Functions and DiseaseR35GM141736 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI ROSEN, MICHAEL K · 2021 to 2025
$1.8M
Class III PI3K as an Autophagy Reactivation Switch in Malignant TransformationK00CA223029 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI YOUNG, LINDSEY N · 2019 to 2022
$295k
Investigating the role of nuclear mechanics in the regulation of chromatin structure and embryonic cell fateK99HD112607 · NICHD · YALE UNIVERSITY · PI SHERRARD, ALICE LOUISA · 2023 to 2024
$249k
Class III PI3K as an Autophagy Reactivation Switch in Malignant TransformationF99CA223029 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI YOUNG, LINDSEY N · 2017 to 2018
$80k
NCI NIH HHS F99 CA223029NCI NIH HHS K00 CA223029NICHD NIH HHS K99 HD112607NIGMS NIH HHS DP2 GM123494NIGMS NIH HHS R01 GM129325NIGMS NIH HHS R35 GM141736
6 · The paper itself

Abstract

In situ cryo-Electron Microscopy (cryo-EM) enables the direct interrogation of structure-function relationships by resolving macromolecular structures in their native cellular environment. Tremendous progress in sample preparation, imaging and data processing over the past decade has contributed to the identification and determination of large biomolecular complexes. However, the majority of proteins are of a size that still eludes identification in cellular cryo-EM data, and most proteins exist in low copy numbers. Therefore, novel tools are needed for cryo-EM to identify the vast majority of macromolecules across multiple size scales (from microns to nanometers). Here, we introduce and validate novel nanogold probes that enable the detection of specific proteins using cryo-ET (cryo-Electron Tomography) and resin-embedded correlated light and electron microscopy (CLEM). We demonstrate that these nanogold probes can be introduced into live cells, in a manner that preserves intact molecular networks and cell viability. We use this system to identify both cytoplasmic and nuclear proteins by room temperature EM, and resolve associated structures by cryo-ET. We further employ gold particles of different sizes to enable future multiplexed labeling and structural analysis. By providing high efficiency protein labeling in live cells and molecular specificity within cryo-ET tomograms, we establish a broadly enabling tool that significantly expands the proteome available to electron microscopy.

Identifiers

PMID39416124
PMCPMC11482945

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.