Evidence map›Paper›PMID 33156335›Full record

ArticleJournal of biomechanical engineering2021

Computational Investigation of Protein Photoinactivation by Molecular Hyperthermia.

Peiyuan Kang, Chen Xie, Oumar Fall, Jaona Randrianalisoa, Zhenpeng Qin

Erratum issuedAbstract read
In one paragraph

Article in Journal of biomechanical engineering, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Nanoparticle Fragmentation Below the Melting Point Under Single Picosecond Laser Pulse Stimulation.The journal of physical chemistry. C, Nanomaterials and interfaces · 2021
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Peiyuan KangDepartment of Mechanical Engineering, University of Texas at Dallas, 800 West Campbell Road, Richardson, TX 75080.
Chen XieDepartment of Mechanical Engineering, University of Texas at Dallas, 800 West Campbell Road, Richardson, TX 75080.
Oumar FallDepartment of Mechanical Engineering, University of Texas at Dallas, 800 West Campbell Road, Richardson, TX 75080;Ecole nationale Supérieure d'Ingénieur de Reims (ESIReims), University of Reims Champagne-Ardenne, 3 Esplanade Roland Garros, Reims 51100, France.
Jaona RandrianalisoaInstitut de Thermique, Mécanique, Matériaux (ITheMM), EA 7548, Université de Reims Champagne-Ardenne, Campus du Moulin de la Housse, F-51687, Reims, France.
Zhenpeng QinDepartment of Mechanical Engineering, Department of Bioengineering, Center for Advanced Pain Studies, University of Texas at Dallas, 800 West Campbell Road, Richardson, TX 75080;Department of Surgery, University of Texas at Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390.

Funding

Optical Control of Protein Activity in Live Cells by Plasmon Assisted Light InactivationR35GM133653 · NIGMS · UNIVERSITY OF TEXAS DALLAS · PI QIN, ZHENPENG · 2019 to 2023
$2.2M
NIGMS NIH HHS R35 GM133653
6 · The paper itself

Abstract

To precisely control protein activity in a living system is a challenging yet long-pursued objective in biomedical sciences. Recently, we have developed a new approach named molecular hyperthermia (MH) to photoinactivate protein activity of interest without genetic modification. MH utilizes nanosecond laser pulse to create nanoscale heating around plasmonic nanoparticles to inactivate adjacent protein in live cells. Here we use a numerical model to study important parameters and conditions for MH to efficiently inactivate proteins in nanoscale. To quantify the protein inactivation process, the impact zone is defined as the range where proteins are inactivated by the nanoparticle localized heating. Factors that reduce the MH impact zone include the laser pulse duration, temperature-dependent thermal conductivity (versus constant properties), and nonspherical nanoparticle geometry. In contrast, the impact zone is insensitive to temperature-dependent material density and specific heat, as well as thermal interface resistance based on reported data in the literature. The low thermal conductivity of cytoplasm increases the impact zone. Different proteins with various Arrhenius kinetic parameters have significantly different impact zones. This study provides guidelines to design the protein inactivation process by MH.

Indexed as

ProteinsNanoparticlesTemperatureThermal ConductivityProteinslocalized heatingmolecular hyperthermiaplasmonic nanoparticleprotein inactivation

Identifiers

PMID33156335
PMCPMC7871998

What OpenQuestion holds

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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.