Evidence map›Paper›PMID 27110027›Full record

ArticleAnalytical chemistry2016

High-Resolution Live-Cell Imaging and Analysis by Laser Desorption/Ionization Droplet Delivery Mass Spectrometry.

Jae Kyoo Lee, Erik T Jansson, Hong Gil Nam, Richard N Zare

Abstract read
In one paragraph

Article in Analytical chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
8.0field-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

21 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Technologies for Decoding Cancer Metabolism with Spatial Resolution.Cold Spring Harbor perspectives in medicine · 2025
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  16. Optically Guided Single Cell Mass Spectrometry of Rat Dorsal Root Ganglia to Profile Lipids, Peptides and Proteins.Chemphyschem : a European journal of chemical physics and physical chemistry · 2018
    Article
  17. Review
  18. Article
  19. microMS: A Python Platform for Image-Guided Mass Spectrometry Profiling.Journal of the American Society for Mass Spectrometry · 2017
    Article
  20. Review
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

4 authors at 3 institutions in 3 countries.

Jae Kyoo LeeDepartment of Chemistry, Stanford University , Stanford, California 94305 United States.
Erik T JanssonDepartment of Chemistry, Stanford University , Stanford, California 94305 United States.
Hong Gil NamCenter for Plant Aging Research, Institute for Basic Science (IBS) , Daegu 42988, Republic of Korea.
Richard N ZareDepartment of Chemistry, Stanford University , Stanford, California 94305 United States.
Stanford University · USDaegu Gyeongbuk Institute of Science and Technology · KRUppsala University · SE

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Melinda L. Telli · 2007 to 2026
$71.4M
High Spatiotemporal Resolution Mass Spectrometry for Single Cell AnalysisR21DA039578 · NIDA · STANFORD UNIVERSITY · PI ZARE, RICHARD N · 2014 to 2015
$427k
NCI NIH HHS P30 CA124435NIDA NIH HHS R21 DA039578
6 · The paper itself

Abstract

We have developed a new ambient-ionization mass spectrometric technique named laser desorption/ionization droplet delivery mass spectrometry (LDIDD-MS). LDIDD-MS permits high-resolution, high-sensitivity imaging of tissue samples as well as measurements of both single-cell apoptosis and live-cell exocytosis. A pulsed (15 Hz) UV laser beam (266 nm) is focused on a surface covered with target analytes to trigger their desorption and ionization. A spray of liquid droplets is simultaneously directed onto the laser-focused surface region to capture the ionized analytes and deliver them to a mass spectrometer. The approach of rapid and effective capturing of molecules after laser desorption/ionization allows the limit of detection for the amino acid lysine to be as low as 2 amol under ambient ionization conditions. Two-dimensional maps of the desorbed/ionized species are recorded by moving the sample on an XY translational stage. The spatial resolution for imaging with LDIDD-MS was determined to be 2.4 μm for an ink-printed pattern and 3 μm for mouse brain tissue. We applied LDIDD-MS to single-cell analysis of apoptotic HEK cells. Differences were observed in the profiles of fatty acids and lipids between healthy HEK cells and those undergoing apoptosis. We observed upregulation of phosphatidylcholine (PC) with a relatively shorter carbon chain length and downregulation of PC with a relatively longer carbon chain length. We also applied LDIDD-MS for a real-time direct measurements of live-cell exocytosis. The catecholamine dopamine and trace amines (phenethylamine and tyramine) were detected from live PC12 cells without damaging them.

Indexed as

Spectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationAmino AcidsAnimalsApoptosisBrainDopamineExocytosisFemaleHEK293 CellsHumansLipid DropletsMiceMice, Inbred C57BLPC12 CellsPhosphatidylcholinesRatsAmino AcidsDopaminePhosphatidylcholines

Identifiers

PMID27110027
PMCPMC5446058
OpenAlexW2340182804

What OpenQuestion holds

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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.