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  • P-ISSN1225-0163
  • E-ISSN2288-8985
  • SCOPUS, ESCI, KCI

Article Detail

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  • P-ISSN 1225-0163
  • E-ISSN 2288-8985

GFP-nanobody-mCherry as a tool for identifying the topology of GFP-fused membrane proteins in intracellular organelles in cells

Analytical Science and Technology / Analytical Science and Technology, (P)1225-0163; (E)2288-8985
2026, v.39 no.1, pp.13-21
https://doi.org/10.5806/AST.2026.39.1.13
Deok-Jin Jang (Department of Vector Entomology, College of Ecology and Environment, Kyungpook National University, Research Institute of Invertebrate Vector, Kyungpook National University, Department of Ecological Science, College of Ecology and Environment, Kyungpook National University)
Minseong Kim (Department of Biopharmaceutical Engineering, College of Life Sciences and Nanotechnology, Hannam University)
Won-Dong Shin (Department of Vector Entomology, College of Ecology and Environment, Kyungpook National University, Research Institute of Invertebrate Vector, Kyungpook National University)
Hun-Joo Kim (Department of Ecological Science, College of Ecology and Environment, Kyungpook National University)
Sang-Won Park (Department of Vector Entomology, College of Ecology and Environment, Kyungpook National University, Research Institute of Invertebrate Vector, Kyungpook National University)
Jin-A Lee (Department of Biological Sciences and Biotechnology, College of Life Sciences and Nanotechnology, Hannam University)

Abstract

A key characteristic of membrane proteins in various intracellular organelles is their topology. The topology of green fluorescent protein (GFP)-tagged transmembrane proteins in membranous organelles can be elucidated using various methods, including protease protection and fluorescence protease protection assays. However, there is still a lack of a simple method to identify topology without disrupting the membrane of the plasma membrane and intracellular organelles, including endoplasmic reticulum and mitochondria. In this study, we demonstrate that GFP nanobody (GNb) fused to mCherry (GNb–mCherry) can be used to identify the topology of GFP-fused membrane proteins in cells. We first demonstrate that cytosolically expressed GNb– mCherry can discriminate cytoplasmic or extracellular or luminal side localization of GFP in GFP-fused plasma membrane, endoplasmic reticulum, Trans-Golgi network, lysosome or mitochondria-targeting proteins. Next, using this assay, we could determine the topology of PRMT8(N20)-GFP in the plasma membrane and mitochondria. Overall, GNb–mCherry can be a useful tool for identifying the topology of GFP-fused membrane proteins in intracellular organelles in cells.

keywords
GFP nanobody, membrane protein, topology, live cell

Graphical Abstract

AST-2025-050_R1_P_Graphical Abstract_001.jpg

Received
2025-10-31
Revised
2025-12-01
Accepted
2025-12-22
Published
2026-02-25
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Analytical Science and Technology