| Autor: |
Phoenix, David A., de Wolf, Frits A., Staffhorst, Rutger W.H.M., Hikita, Chinami, Mizushima, Shoji, Kruijff, Bende |
| Zdroj: |
FEBS Letters; June 1993, Vol. 324 Issue: 1 p113-116, 4p |
| Abstrakt: |
OmpF‐Lpp, a model secretory protein, requires both a positively charged signal sequence and phosphatidylglycerol (PG) for efficient translocation across the E. coliinner membrane. Modification of the signal sequence can, however, remove both these prerequisites for translocation providing OmpF‐Lpp mutants which undergo either PG and charge dependent or PG and charge independent translocation. Here we show that positively charged membrane interactive compounds (polylysine & doxorubicin) are able to inhibit PG dependent translocation of the OmpF‐Lpp signal sequence mutants but not PG independent translocation. Doxorubicin is also shown to bind more efficiently to liposomes containing increased levels of anionic lipid indicating that in these assays it may be inhibiting translocation by preventing electrostatic interaction between the anionic lipid head group and the positively charged signal sequences. |
| Databáze: |
Supplemental Index |
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