Evidence map›Paper›PMID 32144302›Full record

ArticleScientific reports2020

A Modified Magnified Analysis of Proteome (MAP) Method for Super-Resolution Cell Imaging that Retains Fluorescence.

Jiwon Woo, Jeong-Min Seo, Mirae Lee, Juyoung Kim, Sol Min, Sang-Tae Kim, Seockmo Ku, Jeong-Yoon Park

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.1field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

8 authors at 4 institutions in 2 countries.

Jiwon Woo *The Spine and Spinal Cord Institute, Department of Neurosurgery, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, 06273, Republic of Korea.ORCID http://orcid.org/0000-0001-9532-7740
Jeong-Min Seo *Cellular Reprogramming and Embryo Biotechnology Laboratory and Dental Research Institute, Seoul National University School of Dentistry, Seoul, 08826, Republic of Korea.
Mirae LeeThe Spine and Spinal Cord Institute, Department of Neurosurgery, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, 06273, Republic of Korea.
Juyoung KimThe Spine and Spinal Cord Institute, Department of Neurosurgery, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, 06273, Republic of Korea.
Sol MinCellular Reprogramming and Embryo Biotechnology Laboratory and Dental Research Institute, Seoul National University School of Dentistry, Seoul, 08826, Republic of Korea.ORCID http://orcid.org/0000-0003-4260-5780
Sang-Tae KimDepartment of Neurology, Seoul National University Bundang Hospital, Seongnam-si, Gyeonggi-do, 13605, Republic of Korea.
Seockmo KuFermentation Science Program, School of Agriculture, College of Basic and Applied Sciences, Middle Tennessee State University, Murfreesboro, TN, 37132, USA.ORCID http://orcid.org/0000-0003-2661-5073
Jeong-Yoon ParkThe Spine and Spinal Cord Institute, Department of Neurosurgery, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, 06273, Republic of Korea. spinepjy@yuhs.ac.ORCID http://orcid.org/0000-0002-3728-7784
Yonsei University · KRSeoul National University · KRMiddle Tennessee State University · USSeoul National University Bundang Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biological systems consist of a variety of distinct cell types that form functional networks. Super-resolution imaging of individual cells is required for better understanding of these complex systems. Direct visualization of 3D subcellular and nano-scale structures in cells is helpful for the interpretation of biological interactions and system-level responses. Here we introduce a modified magnified analysis of proteome (MAP) method for cell super-resolution imaging (Cell-MAP) which preserves cell fluorescence. Cell-MAP expands cells more than four-fold while preserving their overall architecture and three-dimensional proteome organization after hydrogel embedding. In addition, Optimized-Cell-MAP completely preserves fluorescence and successfully allows for the observation of tagged small molecular probes containing peptides and microRNAs. Optimized-Cell-MAP further successfully applies to the study of structural characteristics and the identification of small molecules and organelles in mammalian cells. These results may give rise to many other applications related to the structural and molecular analysis of smaller assembled biological systems.

Indexed as

FluorescenceAnimalsCell LineCell-Penetrating PeptidesFlow CytometryHEK293 CellsHumansMaleMicroRNAsMicroscopy, FluorescenceProteomeRatsRats, Sprague-DawleyCell-Penetrating PeptidesMicroRNAsProteome

Identifiers

PMID32144302
PMCPMC7060248
OpenAlexW3009080594

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.