Evidence map›Paper›PMID 42814821›Full record

ArticleScience advances2026

Silver(I)-mediated amide-to-ester transformation on unprotected peptides for protein chemical synthesis and engineering.

Zhenquan Sun, Wai Yin Yau, Huajie Kang, Haiyan Zhou, Xin Liu, Zhibo Han, Hongxiang Wu, Xuechen Li

Abstract read
In one paragraph

Article in Science advances, 2026. 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
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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

8 authors.

Zhenquan SunDepartment of Chemistry, State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, P. R. China.ORCID 0000-0003-0877-9015
Wai Yin YauZhongshan Institute for Drug Discovery, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhongshan 528400, P. R. China.
Huajie KangZhongshan Institute for Drug Discovery, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhongshan 528400, P. R. China.ORCID 0009-0006-3976-3357
Haiyan ZhouDepartment of Chemistry, State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, P. R. China.
Xin LiuSchool of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, P. R. China.ORCID 0009-0003-4070-8337
Zhibo HanSchool of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, P. R. China.ORCID 0009-0009-9340-9908
Hongxiang WuZhongshan Institute for Drug Discovery, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Zhongshan 528400, P. R. China.ORCID 0009-0009-1437-7689
Xuechen LiDepartment of Chemistry, State Key Laboratory of Synthetic Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, P. R. China.ORCID 0000-0001-5465-7727

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemical protein synthesis has transformed the preparation of homogeneous peptides and proteins with site-specific modifications. Serine/threonine ligation offers a practical route to access difficult peptides and proteins via its aggregation-breaking intermediate, yet the preparation and regeneration of the prerequisite peptidyl salicylaldehyde ester still require the development of more efficient chemistry. Here, we report a silver(I)-mediated amide-to-ester transformation on unprotected peptides, enabled by an easily introduced

Indexed as

AmidesEstersPeptidesProtein EngineeringSilverHistonesAmidesEstersHistonesPeptidesSilver

Identifiers

PMID42814821
PMCPMC13626038

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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.