Evidence map›Paper›PMID 39511892›Full record

ArticleBiophysical journal2024

Multifocal lipid membrane characterization by combination of DAS-deconvolution and anisotropy.

Natsuumi Ito, Nozomi Morishita Watanabe, Yukihiro Okamoto, Hiroshi Umakoshi

Abstract read
In one paragraph

Article in Biophysical journal, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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0 citing papers in PubMed.

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4 · The record

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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

4 authors.

Natsuumi ItoDivision of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka, Japan.
Nozomi Morishita WatanabeDivision of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka, Japan. Electronic address: no.watanabe.es@osaka-u.ac.jp.
Yukihiro OkamotoDivision of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka, Japan.
Hiroshi UmakoshiDivision of Chemical Engineering, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka, Japan. Electronic address: umakoshi.hiroshi.es@osaka-u.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Three analog solvatochromic probes, Laurdan, Prodan, and Acdan, are extensively used in the study of biological sciences. Their locations in lipid membranes vary greatly in depth, and their fluorescence responds to their surrounding environment based on their corresponding locations in the membrane. Utilizing the fluorescence lifetimes (τ) and emission peak positions (λ) acquired from the time-resolved emission spectrum, one can effectively determine the local lipid environment using the analytical approach, referred to as τ and λ plots. Herein, a τ and λ plot was created using the aforementioned probes to expand the analytical field according to their location. Furthermore, the solvent modeling method in the τ and λ plot was upgraded to artificially emulate the complex environment in lipid membranes by utilizing liquid paraffin and glycerol to assess the contribution of viscosity to each fluorescence distribution. According to the results from a series of solvent mixtures, the effect of solvent viscosity on lifetime values was confirmed in the short lifetime region (τ < 3 ns). However, it was impossible to emulate the longer than 4 ns lifetime values observed in lipid membranes containing 1,2-dipalmitoyl-sn-glycero-3-phosphocholine in the range of viscosity applied in this study. From the insight of the limiting anisotropy (r

Indexed as

Lipid Bilayers2-NaphthylamineAnisotropyFluorescent DyesLauratesSolventsSpectrometry, FluorescenceViscosity2-NaphthylamineFluorescent DyesLaurateslaurdanLipid BilayersSolvents

Identifiers

PMID39511892
PMCPMC11628859

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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.