Evidence map›Paper›PMID 31733279›Full record

ArticleJournal of structural biology2020

Segmentation by classification: A novel and reliable approach for semi-automatic selection of HIV/SIV envelope spikes.

Chaity Banerjee, Moumita Dutta, Xiuwen Liu, Kenneth H Roux, Kenneth A Taylor

Open access · greenAbstract read
In one paragraph

Article in Journal of structural biology, 2020. 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 88% 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, 0 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

5 authors at 1 institution in 1 country.

Chaity BanerjeeDepartment of Computer Science, Florida State University, Tallahassee, FL 32306-4530, United States. Electronic address: chaity.banerjee1@gmail.com.
Moumita DuttaDepartment of Biological Science, Florida State University, Tallahassee, FL 32306-4295, United States. Electronic address: mdutta16@gmail.com.
Xiuwen LiuDepartment of Computer Science, Florida State University, Tallahassee, FL 32306-4530, United States. Electronic address: liux@cs.fsu.edu.
Kenneth H RouxDepartment of Biological Science, Florida State University, Tallahassee, FL 32306-4295, United States. Electronic address: roux@bio.fsu.edu.
Kenneth A TaylorInstitute of Molecular Biophysics, Florida State University, Tallahassee, FL 32306-4380, United States. Electronic address: taylor@bio.fsu.edu.
Florida State University · US

Funding

EM STUDIES ON MUSCLER01GM030598 · NIGMS · FLORIDA STATE UNIVERSITY · PI TAYLOR, KENNETH ALLEN · 1985 to 2020
$4.9M
HIV and SIV Envelope GlycoproteinsR01AI055461 · NIAID · FLORIDA STATE UNIVERSITY · PI ROUX, KENNETH H · 2003 to 2011
$2.8M
Purchase of a FEI Titan Krios for 3-D EMS10RR025080 · NCRR · FLORIDA STATE UNIVERSITY · PI TAYLOR, KENNETH ALLEN · 2008 to 2008
$2.0M
NCRR NIH HHS S10 RR025080NIAID NIH HHS R01 AI055461NIGMS NIH HHS R01 GM030598
6 · The paper itself

Abstract

We describe a semiautomated approach to segment Env spikes from the membrane envelope of Simian Immunodeficiency Virus visualized by cryoelectron tomography of frozen-hydrated specimens. Multivariate data analysis is applied to a large set of overlapping subvolumes extracted semiautomatically from the viral envelope and does not utilize a template of the target structure. The major manual step used in the method involves determination of six points that define an ellipsoid approximating the virion shape. The approach is robust to departures of the actual virion from this starting ellipsoid. A point cage of sufficient density is generated to ensure that any spike-like protein is identified multiple times. Subsequently translational alignment of class averages to a cylindrical reference on a curved surface separates subvolumes with spikes from those without. Spike containing subvolumes identified multiple times are removed by proximity analysis. Slightly different procedures segment spikes in the equatorial and the polar regions. Once all spikes are segmented, further alignment of class averages using separately the polar and spin angles produces recognizable spike images. Our approach localized 96% of the equatorial spikes and 85% of all spikes identified manually; it identifies a significant number of additional spikes missed by manual selection. Two types of spike shapes were segmented, one with near 3-fold symmetry resembling the conventional spike, the other had a T-shape resembling the spike structure obtained when antibodies such as PG9 bind to HIV Env. The approach should be applicable to segmentation of any protein spikes extending from a cellular or virion envelope.

Indexed as

AlgorithmsCryoelectron MicroscopyElectron Microscope Tomographyenv Gene Products, Human Immunodeficiency VirusHIV-1Image Processing, Computer-AssistedSimian Immunodeficiency VirusViral EnvelopeViral ProteinsVirionenv Gene Products, Human Immunodeficiency VirusViral ProteinsCryoelectron microscopyElectron tomographyMembrane proteinsMultivariate data analysis

Identifiers

PMID31733279
PMCPMC8715258
OpenAlexW2988619696

What OpenQuestion holds

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LicenceTDM
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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.