ArticleJournal of molecular modeling2013
Extending the range of FRET--the Monte Carlo study of the antenna effect.
Article in Journal of molecular modeling, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
What it found
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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.
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Who cites it
6 citing papers in PubMed.
- General model of nonradiative excitation energy migration on a spherical nanoparticle with attached chromophores.Scientific reports · 2024Article
- New Core-Shell Nanostructures for FRET Studies: Synthesis, Characterization, and Quantitative Analysis.International journal of molecular sciences · 2022Article
- Article
- Multicolor FRET-FLIM Microscopy to Analyze Multiprotein Interactions in Live Cells.Methods in molecular biology (Clifton, N.J.) · 2021Article
- Dansyl-Labelled Ag@SiOMaterials (Basel, Switzerland) · 2020Article
- FRET from single to multiplexed signaling events.Biophysical reviews · 2017Review
Corrections and comments
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Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
The problem of extending the utilizable range of Förster resonance energy transfer (FRET) is of great current interest, due to the demand of conformation studies of larger biological structures at distances exceeding typical limiting distance of 100 Å. One of the ways to address this issue is the use of so-called antenna effect. In the present work, the influence of the antenna effect on the FRET efficiency is investigated by the Monte Carlo analysis. The previously published results Bojarski et al. (J Phys Chem B 115:10120-10125, 2011) indicate that using a simple model of donor linked with a protein labeled with multiple acceptors, significantly increases the transfer efficiency in comparison with donor-single acceptor system. The effect is stronger if the transition moments of acceptors are mutually parallel. In this work, to extend the scope of possible biological systems to be analyzed, different distributions of donor-acceptors distance are analyzed, as well as the size and shape of the attached molecule.
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