Evidence map›Paper›PMID 39989012›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

A Novel Gene Synthesis Platform for Designing Functional Protein Polymers.

Toshimasa Homma, Rie Yamamoto, Lily Zuin Ping Ang, Alaa Fehaid, Mitsuhiro Ebara

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. A Novel Gene Synthesis Platform for Designing Functional Protein Polymers.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
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

5 authors.

Toshimasa HommaDivision of Chemical Engineering and Biotechnology, National Institute of Technology, Ichinoseki College, Takanashi, Hagisho, Ichinoseki, Iwate, 021-8511, Japan.ORCID https://orcid.org/0000-0002-6215-4764
Rie YamamotoDivision of Chemical Engineering and Biotechnology, National Institute of Technology, Ichinoseki College, Takanashi, Hagisho, Ichinoseki, Iwate, 021-8511, Japan.
Lily Zuin Ping AngDivision of Chemical Engineering and Biotechnology, National Institute of Technology, Ichinoseki College, Takanashi, Hagisho, Ichinoseki, Iwate, 021-8511, Japan.ORCID https://orcid.org/0009-0008-1139-7273
Alaa FehaidDivision of Chemical Engineering and Biotechnology, National Institute of Technology, Ichinoseki College, Takanashi, Hagisho, Ichinoseki, Iwate, 021-8511, Japan.ORCID https://orcid.org/0000-0001-7759-663X
Mitsuhiro EbaraResearch Center for Macromolecules and Biomaterials, National Institute for Materials Science (NIMS), 1-1 Namiki, Tsukuba, Ibaraki, 305-0044, Japan.ORCID https://orcid.org/0000-0002-7906-0350

Funding

Japan Society for the Promotion of Science 22K14549Japan Society for the Promotion of Science 24H01378Ministry of Agriculture, Forestry and Fisheries JP22680575National Institute for Materials Science AM2100New Energy and Industrial Technology Development Organization JPNP20004
6 · The paper itself

Abstract

Recombinant protein polymers with repeat sequences of specific amino acids can be regarded as sustainable functional materials that can be designed using genetic engineering. However, synthesizing genes encoding these proteins is significantly time-consuming and labor-intensive owing to the difficulty of using common gene synthesis tools, such as restriction enzymes and PCR primers. To overcome these obstacles, a novel method is proposed herein: seamless cloning of rolling-circle amplicons (SCRCA). This method involves one-pot preparation of repetitive-sequence genes with overlapping ends for cloning, facilitating the easy construction of the desired recombinants. SCRCA is used to synthesize 10 genes encoding hydrophilic resilin-like and hydrophobic elastin-like repeat units that induce liquid-liquid phase separation. SCRCA shows higher transformation efficiency and better workability than conventional methods, and the time and budget required for SCRCA are comparable to those required for non-repetitive-sequence gene synthesis. Additionally, SCRCA facilitates the construction of a repeat unit library at a low cost. The library shows considerably higher diversity than that of the current state-of-the-art method. By combining this library construction with the directed evolution concept, an elastin-like protein polymer with the desired functions can be rapidly developed. SCRCA can greatly accelerate research on protein polymers.

Indexed as

Genetic EngineeringPolymersProtein EngineeringRecombinant ProteinsCloning, MolecularElastinElastinPolymersRecombinant Proteinsdirected evolutiongene synthesisprotein polymersrepeat sequencesrolling‐circle amplification

Identifiers

PMID39989012
PMCPMC12005822

What OpenQuestion holds

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Registered trials

None linked

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.