Surface Behavior of Sphingomyelins with Very Long Chain Polyunsaturated Fatty Acids and Effects of Their Conversion to Ceramides
Source abstract
Abstract
Molecular species of sphingomyelin (SM) with nonhydroxy (n) and 2-hydroxy (h) very long chain polyunsaturated fatty acids (n- and h-28:4, 30:5, and 32:5) abound in rat spermatogenic cells and spermatozoa. These SMs are located on the sperm head, where they are converted to the corresponding ceramides (Cer) after the completion of the acrosomal reaction, as induced in vitro. The aim of this study was to look into the surface properties of these unique SM species and how these properties change by the SM → Cer conversion. After isolation by HPLC, these SMs were organized in Langmuir films and studied alone, in combination with different proportions of Cer, and during their conversion to Cer by sphingomyelinase. Compression isotherms for all six SMs under study were compatible with a liquid-expanded (LE) state and showed large molecular areas. Only the longest SMs (n-32:5 and h-32:5 SM) underwent a phase transition upon cooling. Interestingly, the abundant h-28:4 Cer exhibited a highly compressible liquid-condensed (LC) phase compatible with a high conformational freedom of Cer molecules but with the characteristic low diffusional properties of the LC phase. In mixed films of h-28:4 SM/h-28:4 Cer, the components showed favorable mixing in the LE phase. The monolayer exhibited h-28:4 Cer-rich domains both in premixed films and when formed by the action of sphingomyelinase on pure h-28:4 SM films. Whereas the SMs from sperm behaved in a way similar to that of shorter acylated SMs, the corresponding Cers showed atypical rheological properties that may be relevant to the membrane structural rearrangements that take place on the sperm head after the completion of the acrosomal reaction.
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
Instituto de Investigaciones Bioquímicas de Bahía Blanca (INIBIBB), Universidad Nacional del Sur and Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), 8000 Bahía Blanca, Argentina
Departamento de Química Biológica, Centro de Investigaciones en Química Biológica de Córdoba (CIQUIBIC), Facultad de Ciencias Químicas, Universidad Nacional de Córdoba and CONICET, 5000 Córdoba, Argentina
References (44)
Show source-provided references
1. Poulos A. · Biochem. J. · 1986 · 240 · 89110.1042/bj2400891 ↗
2. Poulos A. · Biochem. J. · 1987 · 248 · 96110.1042/bj2480961 ↗
3. Sandhoff R. · FEBS Lett. · 2010 · 584 · 190710.1016/j.febslet.2009.12.032 ↗
4. Robinson B. S. · J. Biol. Chem. · 1992 · 267 · 174610.1016/S0021-9258(18)46009-7 ↗
5. Zanetti S. R. · Biochimie · 2010 · 92 · 177810.1016/j.biochi.2010.08.012 ↗
6. Oresti G. M. · Lipids · 2011 · 46 · 108110.1007/s11745-011-3601-x ↗
7. Zanetti S. R. · Biochimie · 2010 · 92 · 188610.1016/j.biochi.2010.08.015 ↗
8. Fanani M. L. · Biochim. Biophys. Acta · 2010 · 1798 · 130910.1016/j.bbamem.2010.01.001 ↗
9. Holopainen J. M. · Biochemistry · 1998 · 37 · 1756210.1021/bi980915e ↗
10. Ruiz-Arguello M. B. · Chem. Phys. Lipids · 2002 · 114 · 1110.1016/S0009-3084(01)00195-5 ↗
11. Boulgaropoulos B. · Biophys. J. · 2010 · 99 · 49910.1016/j.bpj.2010.04.028 ↗
12. Chao L. · Langmuir · 2010 · 26 · 34410.1021/la902084u ↗
13. Peñalva D. A. · J. Lipid Res. · 2013 · 54 · 222510.1194/jlr.M038935 ↗
14. Ramstedt B. · Biochim. Biophys. Acta · 2006 · 1758 · 194510.1016/j.bbamem.2006.05.020 ↗
15. Li X. M. · Biophys. J. · 2003 · 85 · 378810.1016/S0006-3495(03)74794-8 ↗
16. Jaikishan S. · Biochim. Biophys. Acta · 2011 · 1808 · 194010.1016/j.bbamem.2011.04.004 ↗
17. Dupuy F. · Langmuir · 2011 · 27 · 378310.1021/la105011x ↗
18. Brockman H. L. · Biophys. J. · 2004 · 87 · 172210.1529/biophysj.104.044529 ↗
19. Goni F. M. · Biochim. Biophys. Acta · 2006 · 1758 · 190210.1016/j.bbamem.2006.09.011 ↗
20. Peñalva D. A. · Biochim. Biophys. Acta · 2013 · 1838 · 73110.1016/j.bbamem.2013.11.018 ↗
21. Brown R. E. · Methods Mol. Biol. · 2007 · 398 · 4110.1007/978-1-59745-513-8_5 ↗
22. Gaines G. L. · 1966
23. Davies, J. T.; Rideal, E. K.Interfacial Phenomena;Academic Press:New York, 1963; pp217–281.
24. Jungner M. · Biochim. Biophys. Acta · 1997 · 1344 · 23010.1016/S0005-2760(96)00147-6 ↗
25. Wilke N. · Langmuir · 2010 · 26 · 1105010.1021/la100552j ↗
26. Lheveder C. · 2000
27. Li X. M. · Biophys. J. · 2000 · 78 · 192110.1016/S0006-3495(00)76740-3 ↗
28. Fidelio G. D. · Biochim. Biophys. Acta · 1986 · 854 · 23110.1016/0005-2736(86)90115-X ↗
29. Israelachvili J. N. · Q. Rev. Biophys. · 1980 · 13 · 12110.1017/S0033583500001645 ↗
30. Maggio B. · Biochim. Biophys. Acta · 1985 · 815 · 24510.1016/0005-2736(85)90295-0 ↗
31. Israelachvili J. N. · 1992
32. Forstner M. B. · Langmuir · 2001 · 17 · 56710.1021/la000795n ↗
33. Catapano E. R. · Biophys. J. · 2011 · 101 · 272110.1016/j.bpj.2011.10.049 ↗
34. Lopez-Montero I. · Langmuir · 2013 · 29 · 663410.1021/la400448x ↗
35. Martin, A. M.Dynamics of Interfacial Systems. Ph.D. Thesis,Universidad Computense de Madrid, Facultad de Ciencias Químicas, 2010.
36. Busto J. V. · Biophys. J. · 2009 · 97 · 271710.1016/j.bpj.2009.08.040 ↗
37. Leung S. S. · Biophys. J. · 2012 · 103 · 246510.1016/j.bpj.2012.10.041 ↗
38. Fidorra M. · Biochim. Biophys. Acta · 2009 · 1788 · 214210.1016/j.bbamem.2009.08.006 ↗
39. Westerlund B. · Eur. Biophys J. · 2010 · 39 · 111710.1007/s00249-009-0562-6 ↗
40. Hinkovska V. T. · Biochem. Cell Biol. · 1987 · 65 · 52510.1139/o87-067 ↗
41. Nolan J. P. · FASEB J. · 1997 · 11 · 67010.1096/fasebj.11.8.9240968 ↗
42. Flesch F. M. · Biochim. Biophys. Acta · 2000 · 1469 · 19710.1016/S0304-4157(00)00018-6 ↗
43. Holopainen J. M. · Biophys. J. · 2000 · 78 · 83010.1016/S0006-3495(00)76640-9 ↗
44. Goni F. M. · Biochem. Soc. Symp. · 2005 · 72 · 17710.1042/bss0720177 ↗