Engineering Lipid Structure for Recognition of the Liquid Ordered Membrane Phase
Source abstract
Abstract
The selective partitioning of lipid components in phase-separated membranes is essential for domain formation involved in cellular processes. Identifying and tracking the movement of lipids in cellular systems would be improved if we understood how to achieve selective affinity between fluorophore-labeled lipids and membrane assemblies. Here, we investigated the structure and chemistry of membrane lipids to evaluate lipid designs that partition to the liquid ordered (L o ) phase. A range of fluorophores at the headgroup position and lengths of PEG spacer between the lipid backbone and fluorophore were examined. On a lipid body with saturated palmityl or palmitoyl tails, we found that although the lipid tails can direct selective partitioning to the L o phase through favorable packing interactions, headgroup hydrophobicity can override the partitioning behavior and direct the lipid to the disordered membrane phase (L d ). The PEG spacer can serve as a buffer to mute headgroup–membrane interactions and thus improve L o phase partitioning, but its effect is limited with strongly hydrophobic fluorophore headgroups. We present a series of lipid designs leading to the development of novel fluorescently labeled lipids with selective affinity for the L o phase.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Lipid Membrane Structure and Behavior · RNA Interference and Gene Delivery · Sphingolipid Metabolism and Signaling
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Biotechnology and Bioengineering Department, Sandia National Laboratories, Livermore, California 94551, United States
Department of Biomedical Engineering, The University of Texas at Austin, Austin, Texas 78705, United States
Nanosystems Synthesis/Analysis Department, Sandia National Laboratories, Albuquerque, New Mexico 87185, United States
Funding
Basic Energy Sciences · Division of Materials Research
References (34)
Show source-provided references
1. 10.1038/ncb240910.1038/ncb2409 ↗
2. 10.1126/science.285.5425.22110.1126/science.285.5425.221 ↗
3. 10.1126/science.124894310.1126/science.1248943 ↗
4. 10.1126/science.285.5430.102810.1126/science.285.5430.1028 ↗
5. 10.1016/j.coviro.2012.12.00110.1016/j.coviro.2012.12.001 ↗
6. 10.1021/ar970014i10.1021/ar970014i ↗
7. 10.1021/ja00025a05110.1021/ja00025a051 ↗
8. 10.1021/bi900787910.1021/bi9007879 ↗
9. 10.1002/anie.19950905110.1002/anie.199509051 ↗
10. 10.1016/S0006-3495(01)75916-410.1016/S0006-3495(01)75916-4 ↗
11. 10.1038/ncb256110.1038/ncb2561 ↗
12. 10.1126/science.117462110.1126/science.1174621 ↗
13. 10.1016/S0005-2736(03)00021-X10.1016/S0005-2736(03)00021-X ↗
14. 10.1039/b901866b10.1039/b901866b ↗
15. 10.1016/S0006-3495(03)74726-210.1016/S0006-3495(03)74726-2 ↗
16. 10.1016/j.chembiol.2013.11.00910.1016/j.chembiol.2013.11.009 ↗
17. 10.1016/j.bbamem.2012.03.00710.1016/j.bbamem.2012.03.007 ↗
18. 10.1021/bi00567a03910.1021/bi00567a039 ↗
19. 10.1016/j.bbamem.2007.08.02810.1016/j.bbamem.2007.08.028 ↗
20. 10.1016/j.bbamcr.2005.09.00310.1016/j.bbamcr.2005.09.003 ↗
21. 10.1016/j.bbamem.2007.05.01210.1016/j.bbamem.2007.05.012 ↗
22. 10.1039/C4SM02856B10.1039/C4SM02856B ↗
23. 10.1039/dc986810030310.1039/dc9868100303 ↗
24. 10.1111/j.1745-6584.1999.tb01114.x10.1111/j.1745-6584.1999.tb01114.x ↗
25. 10.1529/biophysj.105.08028310.1529/biophysj.105.080283 ↗
26. 10.1021/jp203738m10.1021/jp203738m ↗
27. 10.1371/journal.pone.008764910.1371/journal.pone.0087649 ↗
28. 10.1016/S0006-3495(04)74342-810.1016/S0006-3495(04)74342-8 ↗
29. 10.1021/la104145810.1021/la1041458 ↗
30. 10.1016/j.bbamem.2012.05.02810.1016/j.bbamem.2012.05.028 ↗
31. U.S. National Library of Medicine Toxicology Data Network.http://www.toxnet.nlm.nih.gov.
32. 10.1039/C2FD20107K10.1039/C2FD20107K ↗
33. 10.1021/ja991048j10.1021/ja991048j ↗
34. 10.1021/ja973024n10.1021/ja973024n ↗