Evidence map›Paper›PMID 28603332›Full record

ArticleProceedings of SPIE--the International Society for Optical Engineering2017

Remote focusing multifocal plane microscopy for the imaging of 3D single molecule dynamics with cellular context.

Jerry Chao, Ramraj Velmurugan, Sungyong You, Dongyoung Kim, E Sally Ward, Raimund J Ober

Abstract read
In one paragraph

Article in Proceedings of SPIE--the International Society for Optical Engineering, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 98% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

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

6 authors at 2 institutions in 1 country.

Jerry ChaoDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Ramraj VelmuruganDepartment of Molecular and Cellular Medicine, Texas A&M University Health Science Center, College Station, TX 77843, USA.
Sungyong YouDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Dongyoung KimDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
E Sally WardDepartment of Molecular and Cellular Medicine, Texas A&M University Health Science Center, College Station, TX 77843, USA.
Raimund J OberDepartment of Biomedical Engineering, Texas A&M University, College Station, TX 77843, USA.
Texas A&M University · USTexas A&M Health Science Center · US

Funding

High accuracy quantum dot tracking in live cellsR01GM085575 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI OBER, RAIMUND J · 2008 to 2016
$2.5M
NIGMS NIH HHS R01 GM085575
6 · The paper itself

Abstract

Three-dimensional (3D) single molecule fluorescence microscopy affords the ability to investigate subcellular traffcking at the level of individual molecules. An imaged single molecule trajectory, however, often reveals only limited information about the underlying biological process when insuffcient information is available about the organelles and other cellular structures with which the molecule interacts. A new 3D fluorescence microscopy imaging modality is described here that enables the simultaneous imaging of the trajectories of fast-moving molecules and the associated cellular context. The new modality is called remote focusing multifocal plane microscopy (rMUM), as it extends multifocal plane microscopy (MUM) with a remote focusing module. MUM is a modality that uses multiple detectors to image distinct focal planes within the specimen at the same time, and it has been demonstrated to allow the determination of 3D single molecule trajectories with high accuracy. Remote focusing is a method that makes use of two additional objective lenses to enable the acquisition of a z-stack of the specimen without having to move the microscope's objective lens or sample stage, components which are required by MUM to be fixed in place. rMUM's remote focusing module thus allows the cellular context to be imaged in the form of z-stacks as the trajectories of molecules or other objects of interest are imaged by MUM. In addition to a description of the modality, a discussion of rMUM data analysis and an example of data acquired using an rMUM setup are provided in this paper.

Indexed as

Cellular contextfluorescence microscopymultifocal plane microscopyremote focusingsingle molecule localizationsingle molecule microscopysingle molecule trackingthree-dimensional microscopy

Identifiers

PMID28603332
PMCPMC5463995
OpenAlexW2592775639

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.