Evidence map›Paper›PMID 35296545›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2022

Rapid and Gentle Immunopurification of Brain Synaptic Vesicles.

Mazdak M Bradberry, Shweta Mishra, Zhao Zhang, Lanxi Wu, Justin M McKetney, Martha M Vestling, Joshua J Coon, Edwin R Chapman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
6.3field-weighted citation impact, top 2% of its field
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

12 citing papers in PubMed, 52 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Mazdak M BradberryDepartment of Neuroscience and Howard Hughes Medical Institute, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53705.
Shweta MishraDepartment of Neuroscience and Howard Hughes Medical Institute, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53705.
Zhao ZhangDepartment of Neuroscience and Howard Hughes Medical Institute, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53705.
Lanxi WuDepartment of Neuroscience and Howard Hughes Medical Institute, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53705.
Justin M McKetneyDepartment of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706.
Martha M VestlingDepartment of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706.
Joshua J CoonDepartment of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706.
Edwin R ChapmanDepartment of Neuroscience and Howard Hughes Medical Institute, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin 53705 chapman@wisc.edu.
University of Wisconsin–Madison · USMorgridge Institute for Research · US

Funding

TR&D 2 Metabolic Labels for Ultraplexed Protein Quantification p. 453P41GM108538 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI COON, JOSHUA J · 2016 to 2025
$13.1M
Synaptotagmin C2B Domain as a Ca2+ Sensing ModuleR01MH061876 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI Edwin R Chapman · 2002 to 2026
$7.7M
Integrated Training For Physician-ScientistsT32GM140935 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI Anna Huttenlocher, Jeniel E Nett · 2021 to 2026
$6.5M
Structure and dynamics of exocytotic fusion poresR35NS097362 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI CHAPMAN, EDWIN R · 2017 to 2024
$4.6M
Mechanisms of calcium-dependent neurotransmitter release in health and diseaseF30MH116580 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI BRADBERRY, MAZDAK · 2018 to 2020
$120k
NIGMS NIH HHS P41 GM108538NIGMS NIH HHS T32 GM140935NIMH NIH HHS F30 MH116580NIMH NIH HHS R01 MH061876NINDS NIH HHS R35 NS097362
6 · The paper itself

Abstract

Current methods to isolate synaptic vesicles (SVs), the organellar quanta of synaptic transmission, require highly specialized materials and up to 24 h. These technical obstacles have thus far limited the study of SVs in models of synaptic function and pathophysiology. Here, we describe techniques for the rapid isolation of SVs by immunoprecipitation with widely available antibodies conjugated to magnetic beads. We report that the inexpensive rho1D4 monoclonal antibody binds SVs and show that elution with the 1D4 peptide yields native vesicles that are ≥ 10-fold purer than those obtained with classical techniques. These methods substantially widen the accessibility of SVs, enabling their purification in 60-90 min for downstream analyses including mass spectrometry and cryo-electron microscopy. Immunopurified SV preparations from mouse brain contained apolipoprotein E, the LDL receptor Lrp1, and enzymes involved in lipid metabolism, suggesting that SVs may play direct roles in lipid homeostasis and lipoprotein trafficking at the nerve terminal.

Indexed as

ProteomicsSynaptic VesiclesAnimalsBrainCryoelectron MicroscopyMiceSynaptic Transmissionbiochemistrycryo-electron microscopylipid metabolismneurodegenerationproteomicssynaptic vesicles

Identifiers

PMID35296545
PMCPMC9053850
OpenAlexW4220678623

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.