Evidence map›Paper›PMID 23251551›Full record

ArticlePloS one2012

Anti-candidal activity of genetically engineered histatin variants with multiple functional domains.

Frank G Oppenheim, Eva J Helmerhorst, Urs Lendenmann, Gwynneth D Offner

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. 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
0.7field-weighted citation impact, top 31% 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, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. 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

4 authors at 1 institution in 1 country.

Frank G OppenheimDepartment of Periodontology and Oral Biology, Boston University Henry M. Goldman School of Dental Medicine, Boston, Massachusetts, USA. fropp@bu.edu
Eva J Helmerhorst
Urs Lendenmann
Gwynneth D Offner
Boston University · US

Funding

MICROBICIDAL SALIVARY HISTIDINE-RICH PROTEINSR01DE007652 · NIDCR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI OPPENHEIM, FRANK G · 1986 to 2012
$3.9M
Salivary Proteins in Dental IntegumentsR01DE005672 · NIDCR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI OPPENHEIM, FRANK G · 1985 to 2009
$3.1M
STRUCTURE AND FUNCTION OF HUMAN SALIVARY MUCINSR01DE011691 · NIDCR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI OFFNER, GWYNNETH D · 1996 to 2009
$2.8M
Membrane Bound Mucins in Salivary Glands and SalivaR01DE014080 · NIDCR · BOSTON MEDICAL CENTER · PI OFFNER, GWYNNETH D · 2002 to 2010
$2.2M
Gastro-intestinal microbes degrading dietary glutenR01AI087803 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HELMERHORST, EVA JOSEPHINE · 2010 to 2014
$2.0M
SALIVARY PROTEINS IN DENTAL INTEGUMENTSR37DE005672 · NIDCR · BOSTON UNIVERSITY MEDICAL CAMPUS · PI OPPENHEIM, FRANK G · 1991 to 2000
$411k
MINORITY PREDOCTORAL FELLOWSHIP PROGRAM--NIGMSF31DE005672 · NIDCR · UNIVERSITY OF MARYLAND BALTIMORE · PI MATHURIN, WILLIAM · 1994 to 1997
–
NIAID NIH HHS AI087803NIAID NIH HHS R01 AI087803NIDCR NIH HHS DE05672NIDCR NIH HHS DE07652NIDCR NIH HHS DE11691NIDCR NIH HHS DE14080NIDCR NIH HHS F31 DE005672NIDCR NIH HHS R01 DE005672NIDCR NIH HHS R01 DE007652NIDCR NIH HHS R01 DE011691NIDCR NIH HHS R01 DE014080NIDCR NIH HHS R37 DE005672
6 · The paper itself

Abstract

The human bodily defense system includes a wide variety of innate antimicrobial proteins. Histatins are small molecular weight proteins produced by the human salivary glands that exhibit antifungal and antibacterial activities. While evolutionarily old salivary proteins such as mucins and proline-rich proteins contain large regions of tandem repeats, relatively young proteins like histatins do not contain such repeated domains. Anticipating that domain duplications have a functional advantage, we genetically engineered variants of histatin 3 with one, two, three, or four copies of the functional domain by PCR and splice overlap. The resulting proteins, designated reHst3 1-mer, reHist3 2-mer, reHis3 3-mer and reHist3 4-mer, exhibited molecular weights of 4,062, 5,919, 7,777, and 9,634 Da, respectively. The biological activities of these constructs were evaluated in fungicidal assays toward Candida albicans blastoconidia and germinated cells. The antifungal activities per mole of protein increased concomitantly with the number of functional domains present. This increase, however, was higher than could be anticipated from the molar concentration of functional domains present in the constructs. The demonstrated increase in antifungal activity may provide an evolutionary explanation why such domain multiplication is a frequent event in human salivary proteins.

Indexed as

Genetic EngineeringAmino Acid SequenceAntifungal AgentsCandidaHistatinsHumansInhibitory Concentration 50Microbial Sensitivity TestsMicrobial ViabilityMolecular Sequence DataMutant ProteinsPolymerase Chain ReactionProtein MultimerizationProtein Structure, TertiaryRecombinant ProteinsTime FactorsAntifungal AgentsHistatinsMutant ProteinsRecombinant Proteins

Identifiers

PMID23251551
PMCPMC3520795
OpenAlexW2023204472

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.