2005
DOI: 10.1016/j.bbagen.2005.06.015
|View full text |Cite
|
Sign up to set email alerts
|

Hemolytic activity of new linear surfactin analogs in relation to their physico-chemical properties

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

5
89
0
2

Year Published

2006
2006
2023
2023

Publication Types

Select...
8
1

Relationship

0
9

Authors

Journals

citations
Cited by 104 publications
(96 citation statements)
references
References 37 publications
5
89
0
2
Order By: Relevance
“…It has been shown that surfactin penetration is promoted by longer lipopeptide chain length (Eeman et al, 2006). The data suggested that particularly high hydrophobic lipopeptides have an increased cytotoxic activity on cells (Deleu et al, 2003;Dufour et al, 2005). Furthermore, the significant difference of cytotoxicity in Fig.…”
Section: Discussionmentioning
confidence: 89%
“…It has been shown that surfactin penetration is promoted by longer lipopeptide chain length (Eeman et al, 2006). The data suggested that particularly high hydrophobic lipopeptides have an increased cytotoxic activity on cells (Deleu et al, 2003;Dufour et al, 2005). Furthermore, the significant difference of cytotoxicity in Fig.…”
Section: Discussionmentioning
confidence: 89%
“…Deuterium NMR has revealed that the hydrophobic residues of the peptide moiety penetrate rather deeply into the membrane interface, where they may induce a stronger destabilization than typical detergents (Heerklotz et al 2004). Dufour et al (2005) have shown by comparing cyclic with linear surfactin analogs that the bulky nature of the cyclic peptide group is a prerequisite for membrane permeabilization but not for surface activity, as expected for detergentlike behaviour. The proposal that membranes are permeabilized by dimers of surfactin (Carrillo et al 2003) argues, however, in favor of a more specific mechanism.…”
Section: Introductionmentioning
confidence: 99%
“…RBCs were then washed once in PBS-EDTA 0.075 % and three times in an isotonic buffer (PBS). RBCs were then suspended in this buffer at a cell density of 5-108 cells ml -1 (Dufour et al 2005). Then for hemolysis assay, CH-PVA polymeric blend and CH-PVA/HA nano composite membrane dissolved in small portions of distilled water and 1 M HCl (Chen et al 2004) respectively, and for each sample, prepared solutions in 5, 10, 15 and 20 mg ml -1 concentrations.…”
Section: Hemolysis Assaymentioning
confidence: 99%
“…The negative control prepared by adding 100 ml of RBCs suspension to 900 ml of PBS. The RBCs in PBS remained safe (Dufour et al 2005). Each experiment has been performed at least twice.…”
Section: Hemolysis Assaymentioning
confidence: 99%