Evidence map›Paper›PMID 26764092›Full record

ArticleMolecular biology of the cell2016

A novel imaging method for quantitative Golgi localization reveals differential intra-Golgi trafficking of secretory cargoes.

Hieng Chiong Tie, Divyanshu Mahajan, Bing Chen, Li Cheng, Antonius M J VanDongen, Lei Lu

Abstract read
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Article in Molecular biology of the cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

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0cells of the map it votes in
44citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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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

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3 · Its place in the literature

Who cites it

44 citing papers in PubMed.

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  5. A class of COPI cargo receptors regulates processing of transmembrane proteins by reinforcing their Golgi retention.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  6. Organelles harbour pH gradients.Research square · 2026
    Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Organelles harbour pH gradients.bioRxiv : the preprint server for biology · 2025
    Article
  13. Article
  14. Article
  15. Article
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Hieng Chiong TieSchool of Biological Sciences, Nanyang Technological University, Singapore 637551.
Divyanshu MahajanSchool of Biological Sciences, Nanyang Technological University, Singapore 637551.
Bing ChenSchool of Biological Sciences, Nanyang Technological University, Singapore 637551.
Li ChengBioinformatics Institute, Singapore 138671 School of Computing, National University of Singapore, Singapore 117417.
Antonius M J VanDongenProgram in Neuroscience and Behavioral Disorders, Duke-NUS Graduate Medical School, Singapore 169857.
Lei LuSchool of Biological Sciences, Nanyang Technological University, Singapore 637551 lulei@ntu.edu.sg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cellular functions of the Golgi are determined by the unique distribution of its resident proteins. Currently, electron microscopy is required for the localization of a Golgi protein at the sub-Golgi level. We developed a quantitative sub-Golgi localization method based on centers of fluorescence masses of nocodazole-induced Golgi ministacks under conventional optical microscopy. Our method is rapid, convenient, and quantitative, and it yields a practical localization resolution of ∼ 30 nm. The method was validated by the previous electron microscopy data. We quantitatively studied the intra-Golgi trafficking of synchronized secretory membrane cargoes and directly demonstrated the cisternal progression of cargoes from the cis- to the trans-Golgi. Our data suggest that the constitutive efflux of secretory cargoes could be restricted at the Golgi stack, and the entry of the trans-Golgi network in secretory pathway could be signal dependent.

Indexed as

Cell LineGolgi ApparatusGreen Fluorescent ProteinsHeLa CellsHumansMembrane GlycoproteinsMicroscopy, ConfocalNocodazoleProteinsProtein TransportReproducibility of ResultsTime-Lapse Imagingtrans-Golgi NetworkViral Envelope ProteinsG protein, vesicular stomatitis virusGreen Fluorescent ProteinsMembrane GlycoproteinsNocodazoleProteinsViral Envelope Proteins

Identifiers

PMID26764092
PMCPMC4803310

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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.