Evidence map›Paper›PMID 26696445›Full record

ArticleAngewandte Chemie (International ed. in English)2016

Synthesis of Sulfotyrosine-Containing Peptides by Incorporating Fluorosulfated Tyrosine Using an Fmoc-Based Solid-Phase Strategy.

Wentao Chen, Jiajia Dong, Suhua Li, Yu Liu, Yujia Wang, Leonard Yoon, Peng Wu, K Barry Sharpless, Jeffery W Kelly

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

27 citing papers in PubMed, 61 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Recent Advances of S-ACS omega · 2023
    Review
  11. Fluorosulfate as a Latent Sulfate in Peptides and Proteins.Journal of the American Chemical Society · 2023
    Article
  12. Review
  13. Article
  14. Sulfur fluoride exchange.Nature reviews. Methods primers · 2023
    Article
  15. Article
  16. Article
  17. Sulfur [Journal of the American Chemical Society · 2021
    Article
  18. Article
  19. Article
  20. Review
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

9 authors at 1 institution in 1 country.

Wentao ChenDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Jiajia DongDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Suhua LiDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Yu LiuDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Yujia WangDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Leonard YoonDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA.
Peng WuDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA.
K Barry SharplessDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA. sharples@scripps.edu.
Jeffery W KellyDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA, 92037, USA. jkelly@scripps.edu.
Scripps Research Institute · US

Funding

UNDERSTANDING B-SHEET STRUCTURE IN AQUEOUS SOLUTIONR01GM051105 · NIGMS · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI KELLY, JEFFERY W · 1994 to 2019
$5.8M
NIGMS NIH HHS GM051105NIGMS NIH HHS R01 GM051105
6 · The paper itself

Abstract

Tyrosine O-sulfation is a common protein post-translational modification that regulates many biological processes, including leukocyte adhesion and chemotaxis. Many peptides with therapeutic potential contain one or more sulfotyrosine residues. We report a one-step synthesis for Fmoc-fluorosulfated tyrosine. An efficient Fmoc-based solid-phase peptide synthetic strategy is then introduced for incorporating the fluorosulfated tyrosine residue into peptides of interest. Standard simultaneous peptide-resin cleavage and removal of the acid-labile side-chain protecting groups affords the crude peptides containing fluorosulfated tyrosine. Basic ethylene glycol, serving both as solvent and reactant, transforms the fluorosulfated tyrosine peptides into sulfotyrosine peptides in high yield.

Indexed as

Amino AcidsAmino Acid SequenceFluorenesMolecular Sequence DataPeptidesTyrosineAmino AcidsFluorenesN(alpha)-fluorenylmethyloxycarbonylamino acidsPeptidesTyrosinetyrosine O-sulfateclick chemistrypeptidessolid-phase synthesisSuFExsulfotyrosine

Identifiers

PMID26696445
PMCPMC4928576
OpenAlexW2216192238

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.