Evidence map›Paper›PMID 21596749›Full record

ArticleThe Journal of biological chemistry2011

Anti-heparan sulfate peptides that block herpes simplex virus infection in vivo.

Vaibhav Tiwari, Jian Liu, Tibor Valyi-Nagy, Deepak Shukla

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

77 citing papers in PubMed, 105 citations in OpenAlex.

  1. Review
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  4. Untangling Heparan Sulfate 3-Analytical chemistry · 2025
    Article
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17 more citing papers are in PubMed but not listed here.

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

4 authors at 4 institutions in 1 country.

Vaibhav TiwariDepartments of Ophthalmology and Visual Sciences, University of Illinois, Chicago, Illinois 60612, USA.
Jian Liu
Tibor Valyi-Nagy
Deepak Shukla
University of Illinois Chicago · USUniversity of Illinois Urbana-Champaign · USUniversity of North Carolina at Chapel Hill · USWestern University of Health Sciences · US

Funding

Translational Core for Therapeutic and Diagnostic DevelopmentP30EY001792 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MCANANY, JAMES JASON · 1985 to 2025
$14.8M
In vitro synthesis of recombinant heparan sulfateR01HL094463 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIU, JIAN, PAWLINSKI, RAFAL L · 2009 to 2021
$5.2M
Structural Specificity of Heparan Sulfate for Herpes InfectionsR01AI050050 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI LIU, JIAN · 2001 to 2010
$2.6M
Molecular Mechanism of HSV Entry and SpreadR01AI057860 · NIAID · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHUKLA, DEEPAK · 2005 to 2009
$1.5M
NEI NIH HHS EY001792NEI NIH HHS P30 EY001792NHLBI NIH HHS R01 HL094463NIAID NIH HHS AI050050NIAID NIH HHS R01 AI050050NIAID NIH HHS R01 AI057860
6 · The paper itself

Abstract

Heparan sulfate (HS) and its highly modified form, 3-O-sulfated heparan sulfate (3-OS HS), contribute strongly to herpes simplex virus type-1 (HSV-1) infection in vitro. Here we report results from a random M13-phage display library screening to isolate 12-mer peptides that bind specifically to HS, 3-OS HS, and block HSV-1 entry. The screening identified representative candidates from two-different groups of anti-HS peptides with high positive charge densities. Group 1, represented by G1 peptide (LRSRTKIIRIRH), belongs to a class with alternating charges (XRXRXKXXRXRX), and group 2, represented by G2 peptide (MPRRRRIRRRQK), shows repetitive charges (XXRRRRXRRRXK). Viral entry and glycoprotein D binding assays together with fluorescent microscopy data indicated that both G1 and G2 were potent in blocking HSV-1 entry into primary cultures of human corneal fibroblasts and CHO-K1 cells transiently expressing different glycoprotein D receptors. Interestingly, G2 peptide isolated against 3-OS HS displayed wider ability to inhibit entry of clinically relevant strains of HSV-1 and some divergent members of herpesvirus family including cytomegalovirus and human herpesvirus-8. To identify functional residues within G1 and G2, we performed point mutations and alanine-scanning mutagenesis. Several arginine and a lysine residues were needed for anti-HSV-1 activity, suggesting the importance of the positively charged residues in virus-cell binding and virus-induced membrane fusion. In vivo administration of G1 or G2 peptide as a prophylactic eye drop completely blocked HSV-1 spread in the mouse cornea as evident by immunohistochemistry. This result also highlights an in vivo significance of HS and 3-OS HS during ocular herpes infection.

Indexed as

Amino Acid SubstitutionAnimalsAntiviral AgentsChlorocebus aethiopsCHO CellsCricetinaeCricetulusEye Infections, ViralHeLa CellsHeparan SulfateHerpes SimplexHerpesvirus 1, HumanHumansMiceMice, Inbred BALB CPeptidesAntiviral Agentsglycoprotein D, Human herpesvirus 1Heparan SulfatePeptidesViral Envelope Proteins

Identifiers

PMID21596749
PMCPMC3137111
OpenAlexW4231460886

What OpenQuestion holds

Textmetadata
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.