Evidence map›Paper›PMID 36410375›Full record

ArticleJournal of the American Chemical Society2022

Pentosinane, a Post-Translational Modification of Human Proteins with Underappreciated Stability.

Edward A deRamon, Venkata R Sabbasani, Matthew D Streeter, Yannan Liu, Timothy R Newhouse, David M McDonald, David A Spiegel

Open access · greenAbstract read
In one paragraph

Article in Journal of the American Chemical Society, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 29% of its field
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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Discovery of Glycation-Derived Cross-links at Arginine.Journal of the American Chemical Society · 2026
    Article
  3. The chemical language of protein glycation.Nature chemical biology · 2025
    Review
  4. Review
  5. 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

7 authors at 1 institution in 1 country.

Edward A deRamonDepartment of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520, United States.
Venkata R SabbasaniDepartment of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520, United States.
Matthew D StreeterDepartment of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520, United States.
Yannan LiuDepartment of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520, United States.
Timothy R NewhouseDepartment of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520, United States.ORCID 0000-0001-8741-7236
David M McDonaldDepartment of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520, United States.ORCID 0000-0001-5921-0908
David A SpiegelDepartment of Chemistry, Yale University, 225 Prospect Street, New Haven, Connecticut 06520, United States.ORCID 0000-0002-1102-8012
Yale University · US

Funding

Predoc Training at the Interface Chemistry and BiologyT32GM067543 · NIGMS · YALE UNIVERSITY · PI CRAWFORD, JASON MICHAEL · 2003 to 2022
$7.4M
Synthesis of Neurologically Active Small MoleculesR01GM118614 · NIGMS · YALE UNIVERSITY · PI NEWHOUSE, TIMOTHY · 2017 to 2025
$3.1M
NIGMS NIH HHS R01 GM118614NIGMS NIH HHS T32 GM067543
6 · The paper itself

Abstract

Pentosinane is a structurally complex nonenzymatic post-translational modification of proteins believed to be present in all living things. It falls into the category of advanced glycation end products (AGEs) and is structurally related to the other AGEs pentosidine and glucosepane. Although pentosidine and glucosepane have been widely studied for their role in wide-ranging conditions (e.g., diabetes mellitus, Alzheimer's disease, and human aging), relatively little is known about pentosinane. Interestingly, previous reports have suggested that pentosidine may derive from pentosinane. The (patho)physiological significance of pentosinane in humans is largely unexplored. As a first step to address this knowledge gap, we report herein the first total synthesis of pentosinane. Our synthesis is high yielding (1.7% over seven steps), concise, and enantioselective, and it leverages a strategy for synthesizing 2,5-diaminoimidazoles previously developed by our lab. Access to synthetic pentosinane has allowed us to perform additional studies showing that its oxidation to pentosidine is both pH and oxygen dependent and is substantially slower under physiological conditions than previously believed. Additionally, pentosinane rapidly decomposes under harshly acidic conditions typically employed for pentosidine isolation. Taken together, these results suggest that pentosinane is likely to be more abundant

Indexed as

Protein Processing, Post-TranslationalHumans

Identifiers

PMID36410375
PMCPMC11000625
OpenAlexW4309660899

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.