Mechanisms of Action of Bactericidal/Permeability-Increasing Protein BPI on Reconstituted Outer Membranes of Gram-Negative Bacteria

• Published in: Biochemistry (Easton) Vol. 36; no. 33; pp. 10311 - 10319
• Main Authors: Wiese, Andre, Brandenburg, Klaus, Carroll, Stephen F, Rietschel, Ernst Th, Seydel, Ulrich
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 19.08.1997
• Subjects: Anti-Bacterial Agents - pharmacology; Antimicrobial Cationic Peptides; Blood Proteins - pharmacology; Cell Membrane - drug effects; Gram-Negative Bacteria - drug effects; Membrane Potentials - drug effects; Membrane Proteins; Recombinant Proteins - pharmacology
• ISSN: 0006-2960; 1520-4995
• DOI: 10.1021/bi970177e

The mechanisms of interaction of the recombinant N-terminal portion of bactericidal/permeability-increasing protein, rBPI21, with various planar asymmetric and symmetric bilayer membranes, including the lipid matrix of the outer membrane of Gram-negative bacteria, were investigated via electrical measurements. For the lipopolysaccharide (LPS) leaflet of the outer membrane, isolated deep rough mutant LPS of Escherichia coli strain F515 (F515 LPS) and Proteus mirabilis strain R45 (R45 LPS) were used. The addition of rBPI21 to the LPS side of asymmetric LPS/phospholipid membranes, as well as to black lipid membranes made from dioleoylphosphatidylglycerol (DOPG), led to membrane rupture. The innermembrane potential difference resulted in a slight increase from 0 to 5 mV for symmetric DOPG membranes but changed for asymmetric F515 LPS/PL membranes from −36 to +8 mV and for R45 LPS/PL membranes from −37 to −5 mV following the addition of rBPI21. In all cases, the addition of rBPI21 led to an increase in membrane current. The effect of rBPI21 on the innermembrane potential difference of LPS/PL membranes was significantly reduced in the presence of 40 mM MgCl2 (shift from −36 to −31 mV for F515 LPS). On the basis of these results and from our studies on the interaction of rBPI21 with lipid monolayers and aggregates [Wiese, A., et al. (1997) Biochemistry 36, 10301−10310], a model is discussed explaining how the observed membrane rupture, increase of membrane current, and change of transmembrane potential as induced by rBPI21 may contribute to bacterial dysfunction.