Evidence map›Paper›PMID 22387398›Full record

ArticleAnalytical biochemistry2012

Imaging lysosomal enzyme activity in live cells using self-quenched substrates.

William H Humphries, Christine K Payne

Abstract read
In one paragraph

Article in Analytical biochemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 25% 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

14 citing papers in PubMed, 34 citations in OpenAlex.

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  4. Life science alliance · 2022
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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

2 authors at 1 institution in 1 country.

William H HumphriesSchool of Chemistry and Biochemistry and Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology, Atlanta, GA 30332, USA.
Christine K Payne
Georgia Institute of Technology · US

Funding

Intracellular delivery and targeting of nanoparticlesDP2OD006470 · OD · GEORGIA INSTITUTE OF TECHNOLOGY · PI PAYNE, CHRISTINE K · 2009 to 2009
$2.3M
NIH HHS 1DP2OD006470NIH HHS DP2 OD006470
6 · The paper itself

Abstract

Endocytosis, the internalization and transport of extracellular cargo, is an essential cellular process. The ultimate step in endocytosis is the intracellular degradation of extracellular cargo for use by the cell. While live cell imaging and single particle tracking have been well-utilized to study the internalization and transport of cargo, the final degradation step has required separate biochemical assays. We describe the use of self-quenched endocytic cargo to image the intracellular transport and degradation of endocytic cargo directly in live cells. We first outline the fluorescent labeling and quantification of two common endocytic cargos: a protein, bovine serum albumin, and a lipid nanoparticle, low-density lipoprotein. In vitro measurements confirm that self-quenching is a function of the number of fluorophores bound to the protein or particle and that recovery of the fluorescent signal occurs in response to enzymatic degradation. We then use confocal fluorescence microscopy and flow cytometry to demonstrate the use of self-quenched bovine serum albumin with standard fluorescence techniques. Using live cell imaging and single particle tracking, we find that the degradation of bovine serum albumin occurs in an endo-lysosomal vesicle that is positive for LAMP1.

Indexed as

AnimalsBiological TransportBiomarkersCattleCell LineChlorocebus aethiopsEndocytosisEndosomesEpithelial CellsFlow CytometryFluorescent DyesHydrolasesLipoproteins, LDLLysosomal-Associated Membrane Protein 1LysosomesMicroscopy, ConfocalBiomarkersFluorescent DyesHydrolasesLipoproteins, LDLLysosomal-Associated Membrane Protein 1Serum Albumin, Bovine

Identifiers

PMID22387398
PMCPMC3327787
OpenAlexW2034339581

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.