journal article·2019-04-09Open access

Effects of Amiloride, an Ion Channel Blocker, on Alamethicin Pore Formation in Negatively Charged, Gold-Supported, Phospholipid Bilayers: A Molecular View

Fatemeh Abbasi, ZhangFei Su, Julia Alvarez-Malmagro, J. Jay Leitch, Jacek Lipkowski

Langmuir· Volume 35· Issue 14

Abstract

The effects of amiloride on the structure and conductivity of alamethicin ion pore formation within negatively charged, gold-supported, 1,2-dimyristoyl- sn-glycero-3-phosphocholine/Egg-PG membranes were investigated with the help of electrochemical impedance spectroscopy (EIS), photon polarization modulation-infrared reflection spectroscopy (PM-IRRAS), and atomic force microscopy (AFM). The EIS results indicate that ion conductivity across negatively charged phospholipid bilayers containing alamethicin decreases by an order of magnitude when amiloride is introduced to the system. Despite the reduction in ion conductivity, the PM-IRRAS data shows that amiloride does not inhibit ion channel formation by alamethicin peptides. High-resolution AFM images revealed that amiloride enlarges and distorts the shape of alamethicin ion pores when introduced to the system, indicating that it is inserting itself into the mouth of the alamethicin pores. This effect is driven by electrostatic interactions between positively charged amiloride molecules and the negative charge on the membrane.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Lipid Membrane Structure and Behavior · Electrochemical Analysis and Applications · Electrochemical sensors and biosensors

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, University of Guelph, Guelph, Ontario, Canada N1G 2W1

Funding

Natural Sciences and Engineering Research Council of Canada

References (24)

Show source-provided references
1. 10.1007/BF0187110210.1007/BF01871102 ↗
2. 10.1016/S0956-5663(02)00160-410.1016/S0956-5663(02)00160-4 ↗
3. 10.1016/S1554-4516(05)02002-810.1016/S1554-4516(05)02002-8 ↗
4. 10.1016/S0040-4039(00)02287-510.1016/S0040-4039(00)02287-5 ↗
5. 10.1007/BF0100760710.1007/BF01007607 ↗
6. 10.1002/cbdv.20079009510.1002/cbdv.200790095 ↗
7. 10.1038/300325a010.1038/300325a0 ↗
8. 10.1016/S0006-3495(96)79458-410.1016/S0006-3495(96)79458-4 ↗
9. 10.1007/BF0019691510.1007/BF00196915 ↗
10. 10.1016/0014-5793(83)81105-310.1016/0014-5793(83)81105-3 ↗
11. 10.1073/pnas.120155911010.1073/pnas.1201559110 ↗
12. 10.1016/j.electacta.2018.02.05710.1016/j.electacta.2018.02.057 ↗
13. 10.1021/acs.langmuir.8b0255410.1021/acs.langmuir.8b02554 ↗
14. 10.1016/j.jelechem.2017.12.03910.1016/j.jelechem.2017.12.039 ↗
15. 10.1016/j.jelechem.2017.10.04210.1016/j.jelechem.2017.10.042 ↗
16. 10.1016/j.jelechem.2004.09.03210.1016/j.jelechem.2004.09.032 ↗
17. 10.1016/j.bbamem.2015.12.03510.1016/j.bbamem.2015.12.035 ↗
18. 10.1021/acs.langmuir.7b0426510.1021/acs.langmuir.7b04265 ↗
19. https://avantilipids.com/product/841138.
20. 10.1149/1.210850510.1149/1.2108505 ↗
21. Zamlynny V. · 2006 · 9 · 31510.1002/9783527616817.ch9 ↗
22. 10.1021/la204054g10.1021/la204054g ↗
23. 10.1016/S0006-3495(04)74244-710.1016/S0006-3495(04)74244-7 ↗
24. 10.1016/j.jelechem.2013.10.01510.1016/j.jelechem.2013.10.015 ↗