Evidence map›Paper›PMID 23597400›Full record

ArticleACS chemical biology2013

On-chip synthesis and screening of a sialoside library yields a high affinity ligand for Siglec-7.

Cory D Rillahan, Erik Schwartz, Christoph Rademacher, Ryan McBride, Janani Rangarajan, Valery V Fokin, James C Paulson

Abstract readLetter
In one paragraph

Article in ACS chemical biology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

29 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. Article
  3. New Sialic Acid-Binding Site of SIGLEC-7.Advances in experimental medicine and biology · 2026
    Review
  4. Article
  5. Article
  6. Combatting melioidosis with chemical synthetic lethality.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Siglec Ligands.Cells · 2021
    Review
  17. Probing the binding specificities of human Siglecs by cell-based glycan arrays.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  18. Article
  19. Modulation of immune cell reactivity withProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  20. Terminal Epitope-Dependent Branch Preference of Siglecs TowardFrontiers in molecular biosciences · 2021
    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.

Cory D RillahanDepartments of Cell and Molecular Biology, ‡Chemical Physiology, and §Chemistry, The Scripps Research Institute , 10550 North Torrey Pines Road, La Jolla, California 92037, United States.
Erik Schwartz
Christoph Rademacher
Ryan McBride
Janani Rangarajan
Valery V Fokin
James C Paulson
Max Planck Institute of Colloids and Interfaces · DE

Funding

Treating lung inflammation by targeting SiglecsP01HL107151 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SCHNAAR, RONALD L · 2011 to 2017
$15.4M
REGULATION OF SIALOSIDE EXPRESSION IN LEUKOCYTESR01AI050143 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI PAULSON, JAMES C · 2003 to 2018
$7.0M
INTERDISCIPLINARY TRAINING PROGRAM IN IMMUNOLOGYT32AI007606 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI NEMAZEE, DAVID · 1999 to 2013
$2.1M
Carbon-Heteroatom Bond-Forming ReactionsR01GM087620 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI FOKIN, VALERY V · 2009 to 2013
$1.8M
NHLBI NIH HHS P01 HL107151NHLBI NIH HHS P01HL107151NIAID NIH HHS AI050143NIAID NIH HHS R01 AI050143NIAID NIH HHS T32 AI007606NIAID NIH HHS T32AI007606NIGMS NIH HHS GM087620NIGMS NIH HHS R01 GM087620
6 · The paper itself

Abstract

The Siglec family of sialic acid-binding proteins are differentially expressed on white blood cells of the immune system and represent an attractive class of targets for cell-directed therapy. Nanoparticles decorated with high-affinity Siglec ligands show promise for delivering cargo to Siglec-bearing cells, but this approach has been limited by a lack of ligands with suitable affinity and selectivity. Building on previous work employing solution-phase sialoside library synthesis and subsequent microarray screening, we herein report a more streamlined 'on-chip' synthetic approach. By printing a small library of alkyne sialosides and subjecting these to 'on-chip' click reactions, the largest sialoside analogue library to date was generated. Siglec-screening identified a selective Siglec-7 ligand, which when displayed on liposomal nanoparticles, allows for targeting of Siglec-7(+) cells in peripheral human blood. In silico docking to the crystal structure of Siglec-7 provides a rationale for the affinity gains observed for this novel sialic acid analogue.

Indexed as

Drug Evaluation, PreclinicalAntigens, Differentiation, MyelomonocyticBinding SitesCrystallography, X-RayDrug Delivery SystemsFluoresceinsHumansJurkat CellsLectinsLigandsLiposomesMicroarray AnalysisMolecular StructureSialic AcidsSmall Molecule LibrariesAntigens, Differentiation, MyelomonocyticFluoresceinsLectinsLigandsLiposomesSialic AcidsSIGLEC7 protein, humanSmall Molecule Libraries

Identifiers

PMID23597400
PMCPMC3751994
OpenAlexW2054784782

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.