Evidence map›Paper›PMID 26015281›Full record

ReviewCurrent topics in membranes2015

Dances with Membranes: Breakthroughs from Super-resolution Imaging.

Nikki M Curthoys, Matthew Parent, Michael Mlodzianoski, Andrew J Nelson, Jennifer Lilieholm, Michael B Butler, Matthew Valles, Samuel T Hess

Abstract readReview
In one paragraph

Review in Current topics in membranes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Triarylmethane Fluorophores Resistant to Oxidative Photobluing.Journal of the American Chemical Society · 2019
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. 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

8 authors.

Nikki M CurthoysDepartment of Physics and Astronomy, University of Maine, Orono, ME, USA.
Matthew ParentDepartment of Physics and Astronomy, University of Maine, Orono, ME, USA.
Michael MlodzianoskiDepartment of Physics and Astronomy, University of Maine, Orono, ME, USA.
Andrew J NelsonDepartment of Physics and Astronomy, University of Maine, Orono, ME, USA.
Jennifer LilieholmDepartment of Physics and Astronomy, University of Maine, Orono, ME, USA.
Michael B ButlerDepartment of Physics and Astronomy, University of Maine, Orono, ME, USA.
Matthew VallesDepartment of Physics and Astronomy, University of Maine, Orono, ME, USA.
Samuel T HessDepartment of Physics and Astronomy, University of Maine, Orono, ME, USA.

Funding

Genetic Control of Phospholipid Biosynthesis and Muscular DystrophyR01AR054170 · NIAMS · JACKSON LABORATORY · PI COX, GREGORY A. · 2007 to 2016
$4.4M
The Role of the Actin Cytoskeleton and Cholesterol in Influenza Virus AssemblyR15GM094713 · NIGMS · UNIVERSITY OF MAINE ORONO · PI HESS, SAMUEL T · 2010 to 2010
$425k
Mechanism of Triclosan Disruption of Mast Cell FunctionR15ES024593 · NIEHS · UNIVERSITY OF MAINE ORONO · PI GOSSE, JULIE ANN · 2014 to 2014
$421k
Mechanism of Association between Influenza Hemagglutinin and the Host Cell Actin CytoskeletonR15GM116002 · NIGMS · UNIVERSITY OF MAINE ORONO · PI HESS, SAMUEL T · 2015 to 2015
$337k
NIAMS NIH HHS R01 AR054170NIEHS NIH HHS R15 ES024593NIGMS NIH HHS R15 GM094713NIGMS NIH HHS R15 GM116002
6 · The paper itself

Abstract

Biological membrane organization mediates numerous cellular functions and has also been connected with an immense number of human diseases. However, until recently, experimental methodologies have been unable to directly visualize the nanoscale details of biological membranes, particularly in intact living cells. Numerous models explaining membrane organization have been proposed, but testing those models has required indirect methods; the desire to directly image proteins and lipids in living cell membranes is a strong motivation for the advancement of technology. The development of super-resolution microscopy has provided powerful tools for quantification of membrane organization at the level of individual proteins and lipids, and many of these tools are compatible with living cells. Previously inaccessible questions are now being addressed, and the field of membrane biology is developing rapidly. This chapter discusses how the development of super-resolution microscopy has led to fundamental advances in the field of biological membrane organization. We summarize the history and some models explaining how proteins are organized in cell membranes, and give an overview of various super-resolution techniques and methods of quantifying super-resolution data. We discuss the application of super-resolution techniques to membrane biology in general, and also with specific reference to the fields of actin and actin-binding proteins, virus infection, mitochondria, immune cell biology, and phosphoinositide signaling. Finally, we present our hopes and expectations for the future of super-resolution microscopy in the field of membrane biology.

Indexed as

AnimalsCell MembraneHumansMicrofilament ProteinsMicroscopyMitochondriaModels, BiologicalVirusesMicrofilament ProteinsActinCluster feedbackDomainFPALMLipidLive cellPALMRaftReviewSTORM

Identifiers

PMID26015281
PMCPMC5584789

What OpenQuestion holds

Textmetadata
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.