Evidence map›Paper›PMID 40949228›Full record

ArticleACS omega2025

Liposomes Carrying Surface-Conjugated Trypsin for Controlled Proteolysis Reactions.

Mikiya Wakabayashi, Noriko Yoshimoto, Makoto Yoshimoto

Abstract read
In one paragraph

Article in ACS omega, 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.

Mikiya WakabayashiDepartment of Applied Chemistry, Yamaguchi University, Tokiwadai 2-16-1, Ube 755-8611, Japan.
Noriko YoshimotoDepartment of Applied Chemistry, Yamaguchi University, Tokiwadai 2-16-1, Ube 755-8611, Japan.ORCID https://orcid.org/0000-0002-3171-9953
Makoto YoshimotoDepartment of Applied Chemistry, Yamaguchi University, Tokiwadai 2-16-1, Ube 755-8611, Japan.ORCID https://orcid.org/0000-0001-7489-229X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Control of the proteolytic activity of trypsin is an important challenge in proteomics and food engineering. In this work, trypsin was covalently conjugated to lipid membranes possessing poly-(ethylene glycol) in a 0.1 M sodium phosphate buffer solution (pH = 7.0) to control the enzyme functions using a liposomal environment. The amount of trypsin conjugated per liposome membrane area was maximized based on the size of the polymer chain of liposomes and the type of cross-linker (glutaraldehyde or tris-succinimidyl aminotriacetate). The secondary structure of trypsin was altered through the conjugation reaction, as revealed with circular dichroism measurements and spectral analyses. Stability of trypsin at 40-60 °C significantly increased through being conjugated to liposomes, whereas free trypsin was clearly deactivated even at 40 °C in an enzyme concentration-dependent manner, indicating the involvement of autolysis mechanism. Liposome-conjugated trypsin was applied to catalyze the digestion of bovine serum albumin at 37 °C and a substrate/trypsin weight ratio of 100. The proteolysis rate observed with liposome-conjugated trypsin was smaller than that of the free enzyme, while the rate clearly depended on the characteristics of liposomes. The results obtained demonstrate that liposomes carrying surface-conjugated trypsin are biocompatible, heat stable, and reactivity-controllable catalysts for proteolysis reactions.

Identifiers

PMID40949228
PMCPMC12423795

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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.