Evidence map›Paper›PMID 40926021›Full record

ArticleBiotechnology letters2025

Construction of a bacterial surface display system using split green fluorescent protein (GFP) in Escherichia coli.

Hae Won Kim, Jae Jung Kim, Jong-In Won

Abstract read
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Article in Biotechnology letters, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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

3 authors.

Hae Won KimDepartment of Chemical Engineering, Hongik University, Sangsu-dong, Mapo-gu, Seoul, 04066, Republic of Korea.
Jae Jung KimDepartment of Chemical Engineering, Hongik University, Sangsu-dong, Mapo-gu, Seoul, 04066, Republic of Korea.
Jong-In WonDepartment of Chemical Engineering, Hongik University, Sangsu-dong, Mapo-gu, Seoul, 04066, Republic of Korea. jiwon@hongik.ac.kr.ORCID http://orcid.org/0000-0002-3133-4236

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cell surface display system employs carrier proteins to present target proteins on the outer membrane of cells. This system enables functional proteins to be exposed on the exterior of living cells without cell lysis, allowing direct interaction with the surrounding environment. A major limitation of conventional approaches is the difficulty in displaying large-sized enzymes or antibodies, despite their critical roles in applications requiring functional domains that must remain intact, such as catalytic or antigen-binding sites. To address this challenge, we developed a novel system that enables the surface presentation of target proteins in Escherichia coli by integrating the cell surface display system with the self-assembly of split green fluorescent proteins (GFPs). In this system, GFP11M3 was fused to the carrier protein Lpp-OmpA and displayed on the bacterial surface. The surface-localized Lpp-OmpA-GFP11M3 subsequently assembled with GFP1-10opt, forming a functional GFP complex. By conjugating other target proteins, such as enzymes or antibodies, to GFP1-10opt, these biomolecules can be efficiently displayed on the cell surface. This approach not only facilitates the presentation of large biomolecules but also enables real-time visualization of protein localization through fluorescence detection.

Indexed as

Cell Surface Display TechniquesEscherichia coliGreen Fluorescent ProteinsBacterial Outer Membrane ProteinsEscherichia coli ProteinsRecombinant Fusion ProteinsBacterial Outer Membrane ProteinsEscherichia coli ProteinsGreen Fluorescent ProteinsOMPA outer membrane proteinsRecombinant Fusion ProteinsBacterial surface displayEscherichia coliLpp-OmpASplit GFP

Identifiers

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Registered trials

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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.