Evidence map›Paper›PMID 31348853›Full record

ArticleACS sensors2019

Optical Tracking of Nanometer-Scale Cellular Membrane Deformation Associated with Single Vesicle Release.

Fenni Zhang, Yan Guan, Yunze Yang, Ashley Hunt, Shaopeng Wang, Hong-Yuan Chen, Nongjian Tao

Abstract read
In one paragraph

Article in ACS sensors, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Exocytosis of Nanoparticles: A Comprehensive Review.Nanomaterials (Basel, Switzerland) · 2023
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
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

7 authors.

Fenni ZhangBiodesign Center for Bioelectronics and Biosensors , Arizona State University , Tempe , Arizona 85287 , United States.ORCID 0000-0002-4369-8563
Yan GuanBiodesign Center for Bioelectronics and Biosensors , Arizona State University , Tempe , Arizona 85287 , United States.
Yunze YangBiodesign Center for Bioelectronics and Biosensors , Arizona State University , Tempe , Arizona 85287 , United States.
Ashley HuntBiodesign Center for Bioelectronics and Biosensors , Arizona State University , Tempe , Arizona 85287 , United States.
Shaopeng WangBiodesign Center for Bioelectronics and Biosensors , Arizona State University , Tempe , Arizona 85287 , United States.ORCID 0000-0002-2680-0503
Hong-Yuan ChenState Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering , Nanjing University , Nanjing 210093 , China.
Nongjian TaoBiodesign Center for Bioelectronics and Biosensors , Arizona State University , Tempe , Arizona 85287 , United States.

Funding

A Virion-Display Oscillator Array and Detection Platform for Quantification of Transmembrane Protein Binding KineticsR33CA235294 · NCI · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI WANG, SHAOPENG · 2020 to 2022
$1.1M
Measuring small molecule interactions with membrane proteins on single cells via detecting nanometer scale membrane deformationsR01GM124335 · NIGMS · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI WANG, SHAOPENG · 2017 to 2020
$1.1M
NIGMS NIH HHS R01 GM124335
6 · The paper itself

Abstract

Exocytosis involves interactions between secretory vesicles and the plasma membrane. Studying the membrane response is thus critical to understand this important cellular process and to differentiate different mediator release patterns. Here we introduce a label-free optical imaging method to detect the vesicle-membrane-interaction-induced membrane deformation associated with single exocytosis in mast cells. We show that the plasma membrane expands by a few tens of nanometers accompanying each vesicle-release event, but the dynamics of the membrane deformation varies from cell to cell, which reflect different exocytosis processes. Combining the temporal and spatial information allows us to resolve complex vesicle-release processes, such as two vesicle-release events that occur closely in time and location. Simultaneous following a vesicle release with fluorescence and membrane deformation tracking further allows us to determine the propagation speed of the vesicle-release-induced membrane deformation along the cell surface, which has an average value of 5.2 ± 1.8 μm/s.

Indexed as

Optical ImagingAnimalsCell MembraneExocytosisNanoparticlesParticle SizeRatsSecretory VesiclesTumor Cells, Culturedexocytosislabel-freemast cellmembrane deformationphase contrast imaging

Identifiers

PMID31348853
PMCPMC7007815

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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.