<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>5(1)</volume><submitter>Tang WC</submitter><pubmed_abstract>Lattice lightsheet microscopy (LLSM) featuring three-dimensional recording is improved to manipulate cellular behavior with subcellular resolution through optogenetic activation (optoLLSM). A position-controllable Bessel beam as a stimulation source is integrated into the LLSM to achieve spatiotemporal photoactivation by changing the spatial light modulator (SLM) patterns. Unlike the point-scanning in a confocal microscope, the lattice beams are capable of wide-field optical sectioning for optogenetic activation along the Bessel beam path.We show that the energy power required for optogenetic activations is lower than 1 nW (or 24 mWcm&lt;sup>-2&lt;/sup>) for time-lapses of CRY2olig clustering proteins, and membrane ruffling can be induced at different locations within a cell with subcellular res</pubmed_abstract><journal>Communications biology</journal><pagination>879</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9418249</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Optogenetic manipulation of cell migration with high spatiotemporal resolution using lattice lightsheet microscopy.</pubmed_title><pmcid>PMC9418249</pmcid><pubmed_authors>Tu CH</pubmed_authors><pubmed_authors>Lin YC</pubmed_authors><pubmed_authors>Chen P</pubmed_authors><pubmed_authors>Chang SW</pubmed_authors><pubmed_authors>Yeh CH</pubmed_authors><pubmed_authors>Gao L</pubmed_authors><pubmed_authors>Tang WC</pubmed_authors><pubmed_authors>Lu CH</pubmed_authors><pubmed_authors>Lin YL</pubmed_authors><pubmed_authors>Chen BC</pubmed_authors><pubmed_authors>Hsu TL</pubmed_authors><pubmed_authors>Liu YT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Optogenetic manipulation of cell migration with high spatiotemporal resolution using lattice lightsheet microscopy.</name><description>Lattice lightsheet microscopy (LLSM) featuring three-dimensional recording is improved to manipulate cellular behavior with subcellular resolution through optogenetic activation (optoLLSM). A position-controllable Bessel beam as a stimulation source is integrated into the LLSM to achieve spatiotemporal photoactivation by changing the spatial light modulator (SLM) patterns. Unlike the point-scanning in a confocal microscope, the lattice beams are capable of wide-field optical sectioning for optogenetic activation along the Bessel beam path.We show that the energy power required for optogenetic activations is lower than 1 nW (or 24 mWcm&lt;sup>-2&lt;/sup>) for time-lapses of CRY2olig clustering proteins, and membrane ruffling can be induced at different locations within a cell with subcellular res</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Aug</publication><modification>2025-04-18T22:52:24.84Z</modification><creation>2025-04-07T10:35:27.083Z</creation></dates><accession>S-EPMC9418249</accession><cross_references><pubmed>36028551</pubmed><doi>10.1038/s42003-022-03835-6</doi></cross_references></HashMap>