## Abstract The appearance of multidrug resistance (MDR) of cancer cells is a major obstacle to successful chemotherapy. Several proteins have been identified that pump chemotherapeutic drugs out of cells, thus bringing about MDR. One representative pump is the P‐glycoprotein, whose function can be
Production of Membrane Vesicles by Extrusion: Size Distribution, Enzyme Activity, and Orientation of Plasma Membrane and Chloroplast Inner-Envelope Membrane Vesicles
✍ Scribed by R. Shingles; R.E. Mccarty
- Publisher
- Elsevier Science
- Year
- 1995
- Tongue
- English
- Weight
- 585 KB
- Volume
- 229
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
✦ Synopsis
A comparison of plasma membrane vesicles prepared by a freeze/thaw method was made with vesicles prepared by extrusion through a 100-nm polycarbonate filter. Based on ATPase measurements in the presence or absence of detergent, plasma membrane vesicles were approximately 30% right-side-out in freeze/thaw vesicles, whereas vesicles produced by extrusion were approximately 80% right-side-out. Chloroplast inner-envelope membrane vesicles were loaded with a membrane-impermeant, pH-sensitive fluorophore, pyranine, by either freeze/thaw or extrusion techniques. ATP-linked proton transport activity was considerably lower in vesicles prepared by extrusion compared to vesicles prepared by freeze/thaw. However, total ATPase activity measured as ADP release from ATP was equivalent in both preparations of vesicles. These results suggest that the inner-envelope vesicles produced by extrusion were predominantly oriented right-side-out. Inner-envelope vesicles were loaded internally with phosphate to study proton-linked transport of 3-phosphoglycerate. Vesicle acidification by 3-phosphoglycerate addition was similar in both freeze/thaw and extruded vesicle preparations, indicating that metabolite transport by the phosphate translocator is both functional and bidirectional. These results indicate that extrusion can be used as a method to produce proteoliposomes which are competent for transport studies.
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