Evidence map›Paper›PMID 39795077›Full record

ArticleMolecules (Basel, Switzerland)2024

A Simplified Method for Evaluating Chitin-Binding Activity Applied to YKL-40 (HC-gp39, CHI3L1) and Chitotriosidase.

Keita Suzuki, Hidetoshi Suzuki, Ami Tanaka, Miwa Tanaka, Kairi Takase, Hiromu Takei, Tomoki Kanaizumi, Kazuaki Okawa, Peter O Bauer, Fumitaka Oyama

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. 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. 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

10 authors.

Keita SuzukiDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.
Hidetoshi SuzukiDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.
Ami TanakaDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.
Miwa TanakaDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.
Kairi TakaseDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.
Hiromu TakeiDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.
Tomoki KanaizumiDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.
Kazuaki OkawaDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.
Peter O BauerBioinova a.s., Videnska 1083, 142 00 Prague, Czech Republic.ORCID 0000-0003-2811-1354
Fumitaka OyamaDepartment of Chemistry and Life Science, Kogakuin University, Tokyo 192-0015, Japan.ORCID 0000-0002-1095-8306

Funding

Japan Society for the Promotion of Science 23H02532
6 · The paper itself

Abstract

YKL-40 is structurally similar to chitotriosidase (CHIT1), an active chitinase, but it lacks chitin-degrading activity while retaining chitin-binding capability. Elevated YKL-40 levels are associated with inflammatory diseases and cancers, making it a valuable biomarker. We previously reported that the W69T substitution in YKL-40 significantly reduces its chitin-binding affinity, identifying W69 as a crucial binding site. In this study, we establish a novel chitin-binding affinity evaluation method using a three-step buffer system to assess the binding strength and specificity of chitin-binding proteins and apply it to characterize YKL-40's binding mechanism. Our findings confirm that YKL-40, through its key residue W69, exhibits highly specific and robust affinity to chitin. Unlike CHIT1, which has both a catalytic domain (CatD) and a chitin-binding domain (CBD) that allow for diverse binding and degradation activities, YKL-40 lacks a CBD and is specialized for specific chitin recognition without degrading it. Comparative analysis with YKL-39, which does not contain a corresponding W69 residue, highlights the unique role of this residue in YKL-40's chitin-binding activity that is potentially linked to immune and inflammatory responses. Our evaluation method clarifies YKL-40's binding properties and provides a versatile approach applicable to other chitin-binding proteins.

Indexed as

ChitinChitinase-3-Like Protein 1HexosaminidasesBinding SitesHumansProtein BindingCHI3L1 protein, humanChitinChitinase-3-Like Protein 1chitotriosidaseHexosaminidasescatalytic domain (CatD)chitinchitinase-like proteins (CLPs)chitin-binding activitychitin-binding affinity assaychitin-binding domain (CBD)chitotriosidase (CHIT1)W69 residueYKL-39YKL-40

Identifiers

PMID39795077
PMCPMC11721955

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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.