File Download

  • Find it @ UNIST can give you direct access to the published full text of this article. (UNISTARs only)
Related Researcher

GrzybowskiBartosz Andrzej

Grzybowski, Bartosz A.
Read More

Views & Downloads

Detailed Information

Cited time in webofscience Cited time in scopus
Metadata Downloads

Full metadata record

DC Field Value Language
dc.citation.number 2 -
dc.citation.startPage 270 -
dc.citation.title CELLS -
dc.citation.volume 11 -
dc.contributor.author Polev, Konstantin -
dc.contributor.author Kolygina, Diana V. -
dc.contributor.author Kandere-GrzybowskaKristiana -
dc.contributor.author Grzybowski, Bartosz A. -
dc.date.accessioned 2023-12-21T14:41:58Z -
dc.date.available 2023-12-21T14:41:58Z -
dc.date.created 2022-02-03 -
dc.date.issued 2022-01 -
dc.description.abstract Lysosomes-that is, acidic organelles known for degradation/recycling-move through the cytoplasm alternating between bursts of active transport and short, diffusive motions or even pauses. While their mobility is essential for lysosomes' fusogenic and non-fusogenic interactions with target organelles, their movements have not been characterized in adequate detail. Here, large-scale statistical analysis of lysosomal movement trajectories reveals that lysosome trajectories in all examined cell types-both cancer and noncancerous ones-are superdiffusive and characterized by heavy-tailed distributions of run and flight lengths. Consideration of Akaike weights for various potential models (lognormal, power law, truncated power law, stretched exponential, and exponential) indicates that the experimental data are best described by the lognormal distribution, which, in turn, can be related to one of the space-search strategies particularly effective when "thorough" search needs to balance search for rare target(s) (organelles). In addition, automated, wavelet-based analysis allows for co-tracking the motions of lysosomes and the cargos they carry-particularly the nanoparticle aggregates known to cause selective lysosome disruption in cancerous cells. The methods we describe here could help study nanoparticle assemblies, viruses, and other objects transported inside various vesicle types, as well as coordinated movements of organelles/particles in the cytoplasm. Custom-written code that includes integrated workflow for our analyses is made available for academic use. -
dc.identifier.bibliographicCitation CELLS, v.11, no.2, pp.270 -
dc.identifier.doi 10.3390/cells11020270 -
dc.identifier.issn 2073-4409 -
dc.identifier.scopusid 2-s2.0-85122857937 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/57178 -
dc.identifier.url https://www.mdpi.com/2073-4409/11/2/270 -
dc.identifier.wosid 000747200600001 -
dc.language 영어 -
dc.publisher MDPI -
dc.title Large-Scale, Wavelet-Based Analysis of Lysosomal Trajectories and Co-Movements of Lysosomes with Nanoparticle Cargos -
dc.type Article -
dc.description.isOpenAccess TRUE -
dc.relation.journalWebOfScienceCategory Cell Biology -
dc.relation.journalResearchArea Cell Biology -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordAuthor lysosome transport -
dc.subject.keywordAuthor cancer lysosomes -
dc.subject.keywordAuthor mixed-charge nanoparticles -
dc.subject.keywordAuthor lysosome-nanoparticle co-movement -
dc.subject.keywordAuthor confocal reflection microscopy -
dc.subject.keywordAuthor continuous wavelet transform -
dc.subject.keywordAuthor maximum-likelihood estimates -
dc.subject.keywordAuthor lognormal distribution -
dc.subject.keywordPlus MIXED-CHARGE -
dc.subject.keywordPlus MICROTUBULE DYNAMICS -
dc.subject.keywordPlus CELL -
dc.subject.keywordPlus CANCER -
dc.subject.keywordPlus TRANSPORT -
dc.subject.keywordPlus BEHAVIOR -
dc.subject.keywordPlus DIFFUSION -
dc.subject.keywordPlus DISTRIBUTIONS -
dc.subject.keywordPlus TRAFFICKING -
dc.subject.keywordPlus MOTION -

qrcode

Items in Repository are protected by copyright, with all rights reserved, unless otherwise indicated.