Research Molecular dynamics simulation studies and in vitro site directed mutagenesis of avian beta-defensin Apl_AvBD2 which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Abstract Background: Defensins comprise a group of antimicrobial peptides, widely recognized as important elements of the innate immune system in both animals and plants. Cationicity, rather than the secondary structure, is believed to be the major factor defining the antimicrobial activity of defensins. To test this hypothesis and to improve the activity of the newly identified avian b-defensin Apl_AvBD2 by enhancing the cationicity, we performed in silico site directed mutagenesis, keeping the predicted secondary structure intact. Molecular dynamics (MD) simulation studies were done to predict the activity. Mutant proteins were made by in vitro site directed mutagenesis and recombinant protein expression, and tested for antimicrobial activity to confirm the results obtained in MD simulation analysis.
[1]
W. L. Jorgensen,et al.
Comparison of simple potential functions for simulating liquid water
,
1983
.
[2]
E. Myers,et al.
Basic local alignment search tool.
,
1990,
Journal of molecular biology.
[3]
T. Blundell,et al.
Comparative protein modelling by satisfaction of spatial restraints.
,
1993,
Journal of molecular biology.
[4]
M. Sippl.
Recognition of errors in three‐dimensional structures of proteins
,
1993,
Proteins.
[5]
Gapped BLAST and PSI-BLAST: A new
,
1997
.
[6]
R. Hancock.
Peptide antibiotics
,
1997,
The Lancet.