Evidence map›Paper›PMID 36373962›Full record

ArticleBioinformatics (Oxford, England)2023

Digitally predicting protein localization and manipulating protein activity in fluorescence images using 4D reslicing GAN.

Yang Jiao, Lingkun Gu, Yingtao Jiang, Mo Weng, Mei Yang

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Potential of V-SiJournal of molecular modeling · 2024
    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

5 authors.

Yang JiaoDepartment of Electrical and Computer Engineering, University of Nevada, Las Vegas, NV 89154, USA.ORCID 0000-0002-6390-2517
Lingkun GuSchool of Life Sciences, University of Nevada, Las Vegas, NV 89154, USA.ORCID 0000-0002-6364-0094
Yingtao JiangDepartment of Electrical and Computer Engineering, University of Nevada, Las Vegas, NV 89154, USA.ORCID 0000-0001-7453-9365
Mo WengSchool of Life Sciences, University of Nevada, Las Vegas, NV 89154, USA.
Mei YangDepartment of Electrical and Computer Engineering, University of Nevada, Las Vegas, NV 89154, USA.ORCID 0000-0002-9510-1079

Funding

Outreach/Diversity/Pipeline ProjectP20GM103440 · NIGMS · UNIVERSITY OF NEVADA RENO · PI Jonathan E. Baker · 2012 to 2026
$58.0M
Mechanosensitive remodeling of adherens junctions during snail-driven EMTR00HD088764 · NICHD · UNIVERSITY OF NEVADA LAS VEGAS · PI WENG, MO · 2018 to 2020
$742k
Mechanosensitive remodeling of adherens junctions during snail-driven EMTK99HD088764 · NICHD · PRINCETON UNIVERSITY · PI WENG, MO · 2016 to 2017
$179k
NICHD NIH HHS K99 HD088764NICHD NIH HHS R00 HD088764NIGMS NIH HHS P20 GM103440UNLV TTGRAUNLV University Libraries Open Article Fund
6 · The paper itself

Abstract

motivationWhile multi-channel fluorescence microscopy is a vital imaging method in biological studies, the number of channels that can be imaged simultaneously is limited by technical and hardware limitations such as emission spectra cross-talk. One solution is using deep neural networks to model the localization relationship between two proteins so that the localization of one protein can be digitally predicted. Furthermore, the input and predicted localization implicitly reflect the modeled relationship. Accordingly, observing the response of the prediction via manipulating input localization could provide an informative way to analyze the modeled relationships between the input and the predicted proteins.

resultsWe propose a protein localization prediction (PLP) method using a cGAN named 4D Reslicing Generative Adversarial Network (4DR-GAN) to digitally generate additional channels. 4DR-GAN models the joint probability distribution of input and output proteins by simultaneously incorporating the protein localization signals in four dimensions including space and time. Because protein localization often correlates with protein activation state, based on accurate PLP, we further propose two novel tools: digital activation (DA) and digital inactivation (DI) to digitally activate and inactivate a protein, in order to observing the response of the predicted protein localization. Compared with genetic approaches, these tools allow precise spatial and temporal control. A comprehensive experiment on six pairs of proteins shows that 4DR-GAN achieves higher-quality PLP than Pix2Pix, and the DA and DI responses are consistent with the known protein functions. The proposed PLP method helps simultaneously visualize additional proteins, and the developed DA and DI tools provide guidance to study localization-based protein functions. AVAILABILITY AND IMPLEMENTATION: The open-source code is available at https://github.com/YangJiaoUSA/4DR-GAN. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

Neural Networks, ComputerSoftwareMicroscopy, FluorescenceProbabilityProtein Transport

Identifiers

PMID36373962
PMCPMC9805574

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.