LLPS droplet size estimation via UV–Vis spectroscopy using a microplate reader

M Mayu Enomoto-Kusano T Takashi S. Kodama S Suai Anzawa K Kyoko Furuita (Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Osaka, Suita 565-0871, Japan) R Ryoga Kobayashi N Naotaka Sekiyama W Wataru Togawa T Toshimichi Fujiwara (Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Osaka, Suita 565-0871, Japan) Y Yohei Miyanoiri (Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, 5-1 Myodaiji, Okazaki, Aichi 444-8787, Japan) H Hidehito Tochio C Chojiro Kojima (Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Osaka, Suita 565-0871, Japan)

Abstract

Abstract Liquid-liquid phase separation (LLPS) is critical to the formation of membraneless organelles within cells. Monitoring the size and dynamics of LLPS droplets is essential to understanding their function. However, conventional methods, such as microscopy and dynamic light scattering (DLS), have limitations, including low throughput and complex setups. Here, we present a simple, label-free, high-throughput method for estimating droplet size using ultraviolet-visible (UV–Vis) spectra obtained using a standard microplate reader. This method is theoretically supported by Mie scattering theory. By analyzing the spectral shape and comparing it to that of glass beads of known sizes, our method enables the quantitative estimation of LLPS droplet size in a minimally invasive manner. We validated our approach using peptide droplets of known sizes, then applied it to monitor the growth of protein condensates formed by vesicle-associated membrane protein-associated protein B (VAPB). This technique offers a convenient, scalable alternative for screening LLPS dynamics in various biomolecular systems.

Article Details

Volume / Issue Vol. 16, Issue 1
Published December 27, 2025
ISSN 2045-2322
Publisher Nature Portfolio

Journal Info

Scientific Reports

Nature Portfolio

ISSN: 2045-2322 Open Access Life Sciences

Authors (11)

M

Mayu Enomoto-Kusano

T

Takashi S. Kodama

S

Suai Anzawa

K

Kyoko Furuita

Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Osaka, Suita 565-0871, Japan

R

Ryoga Kobayashi

N

Naotaka Sekiyama

W

Wataru Togawa

T

Toshimichi Fujiwara

Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Osaka, Suita 565-0871, Japan

Y

Yohei Miyanoiri

Exploratory Research Center on Life and Living Systems (ExCELLS), National Institutes of Natural Sciences, 5-1 Myodaiji, Okazaki, Aichi 444-8787, Japan

H

Hidehito Tochio

C

Chojiro Kojima

Institute for Protein Research, Osaka University, 3-2 Yamadaoka, Osaka, Suita 565-0871, Japan