Exchangeable Mimics of DPPC and DPPG Exhibiting Similar Nearest-Neighbor Interactions in Fluid Bilayers
Source abstract
Abstract
The interactions between an exchangeable mimic of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC), Phos(±), with an exchangeable mimic of cholesterol, Chol, have been analyzed in fluid bilayers by means of nearest-neighbor recognition measurements. These interactions have been found to be very similar to those of an exchangeable mimic of 1,2-dipalmitoyl-sn-glycerol-3-phospho-(1'rac-glycerol) (DPPG), Phos(-), interacting with Chol. Thus, both phospholipids have a similar preference for becoming nearest-neighbors of Chol in the liquid-ordered (l0) phase, and both mix, ideally, with Chol in the liquid-disordered (ld) phase. These findings, together with the almost negligible screening effects found for the latter, provide strong evidence that electrostatic forces play a minor role in the preference that both phospholipids have in becoming a favored nearest-neighbor of Chol. They also imply that the main driving force for forming the liquid-ordered phase, and for defining the lateral organization of this phase, is an intrinsic affinity that high-melting lipids and cholesterol have for each other.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Lipid Membrane Structure and Behavior · Sphingolipid Metabolism and Signaling · Surfactants and Colloidal Systems
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemistry, Lehigh University, Bethlehem, Pennsylvania 18015, United States
Funding
Division of Chemistry
References (25)
Show source-provided references
1. 10.1021/bi971167g10.1021/bi971167g ↗
2. 10.1126/science.117462110.1126/science.1174621 ↗
3. 10.1016/j.bbamem.2013.10.01910.1016/j.bbamem.2013.10.019 ↗
4. 10.1016/S0006-3495(01)76245-510.1016/S0006-3495(01)76245-5 ↗
5. 10.1016/j.bpj.2012.03.04310.1016/j.bpj.2012.03.043 ↗
6. 10.1016/j.bpj.2014.03.01710.1016/j.bpj.2014.03.017 ↗
7. 10.1016/j.bbamem.2008.08.00710.1016/j.bbamem.2008.08.007 ↗
8. 10.1038/ncb0107-710.1038/ncb0107-7 ↗
9. 10.1016/j.bpj.2014.03.01810.1016/j.bpj.2014.03.018 ↗
10. 10.1529/biophysj.107.11496710.1529/biophysj.107.114967 ↗
11. 10.1021/la500510s10.1021/la500510s ↗
12. 10.1021/ja410566710.1021/ja4105667 ↗
13. Nagarajan, R.Amphiphilic Surfactants and Amphiphilic Polymers: Principles of Molecular Assembly in Amphiphiles: Molecular Assembly and Applications;ACS Symposium Series1070;American Chemical Society:Washington, DC, 2011; pp1–22.10.1021/bk-2011-1070.ch001 ↗
14. 10.1039/C4SM01089B10.1039/C4SM01089B ↗
15. 10.1021/ar500260t10.1021/ar500260t ↗
16. 10.1039/c2sc20098h10.1039/c2sc20098h ↗
17. 10.1021/bi00605a02310.1021/bi00605a023 ↗
18. 10.1021/la701503v10.1021/la701503v ↗
19. 10.1021/la001065i10.1021/la001065i ↗
20. 10.1073/pnas.88.19.868610.1073/pnas.88.19.8686 ↗
21. 10.1021/la203527810.1021/la2035278 ↗
22. 10.1016/j.bbamem.2007.07.00910.1016/j.bbamem.2007.07.009 ↗
23. 10.1016/j.bbamem.2009.08.00410.1016/j.bbamem.2009.08.004 ↗
24. 10.1016/j.bpj.2015.07.03610.1016/j.bpj.2015.07.036 ↗
25. 10.1016/j.bpj.2015.07.03710.1016/j.bpj.2015.07.037 ↗