Bengt Erik Haug

Prof. Dr. Bengt Erik Haug

Department of Chemistry and Centre for Pharmacy, University of Bergen, Allégaten 41, NO-5007 Bergen, Norway
orcid

Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
29 March 2003 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
MSMorten B. Strøm
Morten B. Strøm
Bengt Erik HaugBengt Erik Haug
Bengt Erik Haug
MSMerete L. Skar
Merete L. Skar
WSWenche Stensen
Wenche Stensen
TSTrine Stiberg
Trine Stiberg
JSJohn S. Mjøen Svendsen
John S. Mjøen Svendsen

21 June 2008 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
Bengt Erik HaugBengt Erik Haug
Bengt Erik Haug
WSWenche Stensen
Wenche Stensen
MKManar Kalaaji
Manar Kalaaji
ØRØystein Rekdal
Øystein Rekdal
JSJohn S. Mjøen Svendsen
John S. Mjøen Svendsen

1 February 2002 in Biochemistry and Cell Biology
Verified
Journal Article
Closed access
MSMorten B. Strøm
Morten B. Strøm
Bengt Erik HaugBengt Erik Haug
Bengt Erik Haug
ØRØystein Rekdal
Øystein Rekdal
MSMerete L Skar
Merete L Skar
WSWenche Stensen
Wenche Stensen
JSJohn S. Mjøen Svendsen
John S. Mjøen Svendsen
This review focuses on important structural features affecting the antimicrobial activity of 15-residue derivatives of lactoferricins. Our investigations are based on an alanine-scan of a 15-residue bovine lactoferricin derivative that revealed the absolute necessity of two tryptophan residues for antimicrobial activity. This "tryptophan-effect" was further explored in homologous derivatives of human, caprine, and porcine lactoferricins by the incorporation of one additional tryptophan residue, and by increasing the content of tryptophan in the bovine derivative to five residues. Most of the resulting peptides display a substantial increase in antimicrobial activity. To identify which molecular properties make tryptophan so effective, a series of bovine lactoferricin derivatives were prepared containing non-encoded unnatural aromatic amino acids, which represented various aspects of the physicochemical nature of tryptophan. The results clearly demonstrate that tryptophan is not unique since most of the modified peptides were of higher antimicrobial potency than the native peptide. The size and three-dimensional shape of the inserted "super-tryptophans" are the most important determinants for the high antimicrobial activity of the modified peptides. This review also describes the use of a "soft-modeling" approach in order to identify important structural parameters affecting the antimicrobial activity of modified 15-residue murine lactoferricin derivatives. This QSAR-study revealed that the net charge, charge asymmetry, and micelle affinity of the peptides were the most important structural parameters affecting their antimicrobial activity.Key words: antimicrobial peptides, lactoferricin, non-encoded aromatic amino acids, tryptophan.

29 February 2008 in Biochemistry
Verified
Journal Article
Closed access
JSJohan Svenson
Johan Svenson
WSWenche Stensen
Wenche Stensen
BBBjørn-Olav Brandsdal
Bjørn-Olav Brandsdal
Bengt Erik HaugBengt Erik Haug
Bengt Erik Haug
JMJohnny Monrad
Johnny Monrad
JSJohn S. Mjøen Svendsen
John S. Mjøen Svendsen

29 March 2016
Verified
Closed access
Bengt Erik HaugBengt Erik Haug
Bengt Erik Haug
KCKetil André Camilio
Ketil André Camilio
LELiv Tone Eliassen
Liv Tone Eliassen
WSWenche Stensen
Wenche Stensen
JSJohn S. Mjøen Svendsen
John S. Mjøen Svendsen
ØRØystein Rekdal
Øystein Rekdal

16 July 2004 in Journal of Medicinal Chemistry
Verified
Journal Article
Closed access
Bengt Erik HaugBengt Erik Haug
Bengt Erik Haug
WSWenche Stensen
Wenche Stensen
TSTrine Stiberg
Trine Stiberg
JSJohn S. Mjøen Svendsen
John S. Mjøen Svendsen