Influence of disulfide bonds in human beta defensin-3 on its strain specific activity against Gram-negative bacteria

• Published in: Biochimica et biophysica acta. Biomembranes 2020-08, Vol.1862 (8), p.183273-183273, Article 183273
• Main Authors: Nehls, Christian, Böhling, Arne, Podschun, Rainer, Schubert, Sabine, Grötzinger, Joachim, Schromm, Andra, Fedders, Henning, Leippe, Matthias, Harder, Jürgen, Kaconis, Yani, Gronow, Sabine, Gutsmann, Thomas
• Format: Article
• Language: English
• ISSN: 0005-2736; 1879-2642
• DOI: 10.1016/j.bbamem.2020.183273

Antimicrobial peptides (AMPs) play an important role in the host defense against various microbes. One of the most efficient human AMPs is the human beta defensin-3 (hBD-3) which is produced by, e.g. keratinocytes and lung epithelial cells. However, the structure-function relationship for AMPs and in particular for defensins with their typical three disulfide bonds is still poorly understood. In this study the importance of the three disulfide bonds for the activity of the AMPs is investigated with biological assays and with biophysical experiments utilizing different membrane reconstitution systems. The activities of natural hBD-3, hBD-3-c (cyclic variant with one disulfide bond), and hBD-3-l (linear variant without disulfide bonds) and fragments thereof were tested against specific Gram-negative bacteria. Furthermore, hemolytic and cytotoxic activities were analyzed as well as the potency to neutralize immune cell stimulation of lipopolysaccharide (LPS). Experiments using reconstituted lipid matrices composed of phospholipids or LPS purified from the respective Gram-negative bacteria, showed that the membrane activity of all three hBD-3 peptides is decisive for their capability to kill bacteria and to neutralize LPS. In most of the test systems the linear hBD-3-l showed the highest activity. It was also the only peptide significantly active against polymyxin B-resistant Proteus mirabilis R45. However, the stability of hBD-3 against protease activity decreases with decreasing number of disulfide bonds. This study demonstrates that the refining of AMP structures can generate more active compounds against certain strains. [Display omitted]