Native Planar Asymmetric Suspended Membrane for Single‐Molecule Investigations: Plasma Membrane on a Chip
Source abstract
Abstract
Abstract Cellular plasma membranes, in their role as gatekeepers to the external environment, host numerous protein assemblies and lipid domains that manage the movement of molecules into and out of cells, regulate electric potential, and direct cell signaling. The ability to investigate these roles on the bilayer at a single‐molecule level in a controlled, in vitro environment while preserving lipid and protein architectures will provide deeper insights into how the plasma membrane works. A tunable silicon microarray platform that supports stable, planar, and asymmetric suspended lipid membranes (SLIM) using synthetic and native plasma membrane vesicles for single‐molecule fluorescence investigations is developed. Essentially, a “plasma membrane‐on‐a‐chip” system that preserves lipid asymmetry and protein orientation is created. By harnessing the combined potential of this platform with total internal reflection fluorescence (TIRF) microscopy, the authors are able to visualize protein complexes with single‐molecule precision. This technology has widespread applications in biological processes that happen at the cellular membranes and will further the knowledge of lipid and protein assemblies.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Lipid Membrane Structure and Behavior · Nanopore and Nanochannel Transport Studies · Microfluidic and Bio-sensing Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Nanobiology Institute Yale University School of Medicine West Haven CT 06516 USA
Department of Cell Biology Yale University School of Medicine New Haven CT 06520 USA
Department of Pathology Yale University School of Medicine New Haven CT 06520 USA
Department of Neurology Yale University School of Medicine New Haven CT 06520 USA
References (64)
Show source-provided references
1. 10.1126/science.175.4023.72010.1126/science.175.4023.720 ↗
2. 10.1016/S0022-2275(20)43097-410.1016/S0022-2275(20)43097-4 ↗
3. 10.1038/nprot.2013.06110.1038/nprot.2013.061 ↗
4. 10.1007/978-1-4939-8760-3_1510.1007/978-1-4939-8760-3_15 ↗
5. 10.1038/nprot.2006.16610.1038/nprot.2006.166 ↗
6. 10.1021/nn506494e10.1021/nn506494e ↗
7. 10.1021/acsnano.0c0166510.1021/acsnano.0c01665 ↗
8. 10.1016/j.chemphyslip.2019.05.00210.1016/j.chemphyslip.2019.05.002 ↗
9. 10.1126/science.aad996410.1126/science.aad9964 ↗
10. 10.1073/pnas.100183110710.1073/pnas.1001831107 ↗
11. 10.1016/j.bpj.2010.03.01310.1016/j.bpj.2010.03.013 ↗
12. 10.1039/D1LC01077H10.1039/D1LC01077H ↗
13. 10.1016/j.snb.2020.12891710.1016/j.snb.2020.128917 ↗
14. 10.1021/ja073174q10.1021/ja073174q ↗
15. 10.1021/acsbiomaterials.5b0020510.1021/acsbiomaterials.5b00205 ↗
16. 10.3390/ma512270510.3390/ma5122705 ↗
17. 10.1016/S0006-3495(03)74881-410.1016/S0006-3495(03)74881-4 ↗
18. 10.1002/adma.20070046810.1002/adma.200700468 ↗
19. 10.1038/194979a010.1038/194979a0 ↗
20. 10.1007/978-1-4757-1361-910.1007/978-1-4757-1361-9 ↗
21. 10.1021/jp983996x10.1021/jp983996x ↗
22. 10.1002/chem.20070052110.1002/chem.200700521 ↗
23. 10.1021/la052387v10.1021/la052387v ↗
24. 10.1038/s41598-017-15103-310.1038/s41598-017-15103-3 ↗
25. 10.1146/annurev.bi.48.070179.00040310.1146/annurev.bi.48.070179.000403 ↗
26. 10.1016/j.bpj.2018.11.313810.1016/j.bpj.2018.11.3138 ↗
27. 10.1016/j.bpj.2020.05.02310.1016/j.bpj.2020.05.023 ↗
28. 10.1007/s00249-020-01479-010.1007/s00249-020-01479-0 ↗
29. 10.1021/acs.nanolett.8b0224010.1021/acs.nanolett.8b02240 ↗
30. 10.1002/smll.20190072510.1002/smll.201900725 ↗
31. 10.1021/acs.langmuir.8b0011610.1021/acs.langmuir.8b00116 ↗
32. 10.7554/eLife.7193810.7554/eLife.71938 ↗
33. 10.1016/j.celrep.2017.12.05610.1016/j.celrep.2017.12.056 ↗
34. 10.1002/1873-3468.1331710.1002/1873-3468.13317 ↗
35. 10.7554/eLife.5450610.7554/eLife.54506 ↗
36. Axelrod D. · 2008 · 16910.1016/S0091-679X(08)00607-9 ↗
37. 10.1016/S0360-3016(02)03928-710.1016/S0360-3016(02)03928-7 ↗
38. 10.1126/science.274.5294.185910.1126/science.274.5294.1859 ↗
39. 10.1039/c2nr12039a10.1039/c2nr12039a ↗
40. 10.1016/B978-0-12-420138-5.00019-710.1016/B978-0-12-420138-5.00019-7 ↗
41. 10.1002/1873-3468.1415710.1002/1873-3468.14157 ↗
42. 10.1038/nsmb.309710.1038/nsmb.3097 ↗
43. 10.1016/j.bbamem.2019.18303310.1016/j.bbamem.2019.183033 ↗
44. 10.1074/jbc.M111.24452510.1074/jbc.M111.244525 ↗
45. 10.1155/2011/20845710.1155/2011/208457 ↗
46. 10.1016/j.bpj.2010.04.06310.1016/j.bpj.2010.04.063 ↗
47. 10.1038/nsmb.210310.1038/nsmb.2103 ↗
48. 10.1007/978-1-4939-1752-5_610.1007/978-1-4939-1752-5_6 ↗
49. 10.1126/science.98204410.1126/science.982044 ↗
50. 10.1038/nprot.2012.05910.1038/nprot.2012.059 ↗
51. 10.2174/15672050778301830710.2174/156720507783018307 ↗
52. 10.1016/j.neuron.2008.02.00310.1016/j.neuron.2008.02.003 ↗
53. 10.1016/j.neuro.2008.02.01110.1016/j.neuro.2008.02.011 ↗
54. 10.1038/nchem.253710.1038/nchem.2537 ↗
55. 10.1021/am101191d10.1021/am101191d ↗
56. 10.1021/ja204085910.1021/ja2040859 ↗
57. 10.1016/j.cell.2006.10.03010.1016/j.cell.2006.10.030 ↗
58. 10.1016/S0076-6879(03)72016-310.1016/S0076-6879(03)72016-3 ↗
59. 10.1038/nsmb.257010.1038/nsmb.2570 ↗
60. 10.1021/acsnano.0c0133010.1021/acsnano.0c01330 ↗
61. 10.1371/journal.pone.015845710.1371/journal.pone.0158457 ↗
62. 10.1016/j.bpj.2010.04.06310.1016/j.bpj.2010.04.063 ↗
63. 10.1002/1873-3468.1400610.1002/1873-3468.14006 ↗
64. 10.1021/acs.langmuir.5b0117310.1021/acs.langmuir.5b01173 ↗