journal article·2021-08-04

Correlation between Protonation of Tailor-Made Polypiperazines and Endosomal Escape for Cytosolic Protein Delivery

Franziska Hausig, Fabian H. Sobotta, Friederike Richter, Dominic O. Harz, Anja Traeger, Johannes C. Brendel

ACS Applied Materials & Interfaces· Volume 13· Issue 30
Publisher page

Abstract

Responsive polymers, which become protonated at decreasing pH, are considered a milestone in the development of synthetic cell entry vectors. Exact correlations between their properties and their ability to escape the endosome, however, often remain elusive due to hydrophobic interactions or limitations in the design of water-soluble materials with suitable basicity. Here, we present a series of well-defined, hydrophilic polypiperazines, where systematic variation of the amino moiety facilitates an unprecedented fine-tuning of the basicity or pKa value within the physiologically relevant range (pH 6–7.4). Coincubation of HEK 293T cells with various probes, including small fluorophores or functioning proteins, revealed a rapid increase of endosomal release for polymers with pKa values above 6.5 or 7 in serum-free or serum-containing media, respectively. Similarly, cytotoxic effects became severe at increased pKa values (>7). Although the window for effective transport appears narrow, the discovered correlations offer a principal guideline for the design of effective polymers for endosomal escape.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: RNA Interference and Gene Delivery · Advanced biosensing and bioanalysis techniques · Lipid Membrane Structure and Behavior

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

Affiliations

Laboratory of Organic and Macromolecular Chemistry (IOMC), Friedrich Schiller University Jena, Humboldtstrasse 10, 07743 Jena, Germany

Jena Center for Soft Matter (JCSM), Friedrich Schiller University Jena, Philosophenweg 7, 07743 Jena, Germany

Funding

Bundesministerium für Bildung und Forschung · Deutsche Forschungsgemeinschaft · Verband der Chemischen Industrie

References (70)

Show source-provided references
1. 10.1038/nbt.333010.1038/nbt.3330 ↗
2. 10.1039/c7py01603d10.1039/c7py01603d ↗
3. 10.1021/acs.bioconjchem.8b0077810.1021/acs.bioconjchem.8b00778 ↗
4. 10.1016/j.copbio.2010.06.01110.1016/j.copbio.2010.06.011 ↗
5. 10.1073/pnas.190665311610.1073/pnas.1906653116 ↗
6. 10.1038/s41417-019-0141-710.1038/s41417-019-0141-7 ↗
7. 10.1016/j.jconrel.2019.05.01510.1016/j.jconrel.2019.05.015 ↗
8. 10.1515/bmc-2017-002310.1515/bmc-2017-0023 ↗
9. 10.3390/biom803005010.3390/biom8030050 ↗
10. 10.1038/s41467-019-12906-y10.1038/s41467-019-12906-y ↗
11. 10.1021/acs.bioconjchem.8b0073210.1021/acs.bioconjchem.8b00732 ↗
12. 10.1083/jcb.131.1.11110.1083/jcb.131.1.111 ↗
13. 10.1016/j.addr.2003.10.04110.1016/j.addr.2003.10.041 ↗
14. 10.1021/acs.chemrev.7b0067810.1021/acs.chemrev.7b00678 ↗
15. 10.1038/nmeth.299810.1038/nmeth.2998 ↗
16. 10.1002/marc.20140012010.1002/marc.201400120 ↗
17. 10.1039/d0tb00340a10.1039/d0tb00340a ↗
18. 10.1002/marc.20190066810.1002/marc.201900668 ↗
19. Maxfield F. R. · 1987 · 18910.1007/978-1-4684-5442-0_16 ↗
20. Wagner E. · 2014 · 88 · 231
21. 10.1021/cr500679310.1021/cr5006793 ↗
22. 10.1021/acs.biomac.9b0099910.1021/acs.biomac.9b00999 ↗
23. 10.1016/j.jconrel.2006.04.01410.1016/j.jconrel.2006.04.014 ↗
24. 10.1016/j.jconrel.2019.10.04610.1016/j.jconrel.2019.10.046 ↗
25. 10.1016/j.ejpb.2004.11.01110.1016/j.ejpb.2004.11.011 ↗
26. 10.1073/pnas.92.16.729710.1073/pnas.92.16.7297 ↗
27. 10.1038/mt.2012.18510.1038/mt.2012.185 ↗
28. 10.1021/acs.accounts.6b0020010.1021/acs.accounts.6b00200 ↗
29. 10.1039/c8tb00967h10.1039/c8tb00967h ↗
30. 10.1021/mz300660t10.1021/mz300660t ↗
31. 10.1021/bm500452710.1021/bm5004527 ↗
32. 10.1021/acs.bioconjchem.8b0007410.1021/acs.bioconjchem.8b00074 ↗
33. 10.1016/j.biomaterials.2018.05.04610.1016/j.biomaterials.2018.05.046 ↗
34. 10.1039/c6py01872f10.1039/c6py01872f ↗
35. 10.1021/la500758310.1021/la5007583 ↗
36. 10.1016/j.ejpb.2012.08.00210.1016/j.ejpb.2012.08.002 ↗
37. 10.1038/ncomms290510.1038/ncomms2905 ↗
38. 10.1016/j.nano.2013.07.00810.1016/j.nano.2013.07.008 ↗
39. 10.1021/acs.biomac.5b0028610.1021/acs.biomac.5b00286 ↗
40. 10.1002/cmdc.20060000810.1002/cmdc.200600008 ↗
41. 10.1021/bm034041+10.1021/bm034041+ ↗
42. 10.1002/wnan.145210.1002/wnan.1452 ↗
43. 10.1021/ma000928b10.1021/ma000928b ↗
44. 10.1002/app.2712610.1002/app.27126 ↗
45. 10.1126/sciadv.aaw892210.1126/sciadv.aaw8922 ↗
46. 10.1186/s12951-014-0041-910.1186/s12951-014-0041-9 ↗
47. 10.1021/jp301237710.1021/jp3012377 ↗
48. 10.1021/ed074p93710.1021/ed074p937 ↗
49. 10.1039/d0py01697g10.1039/d0py01697g ↗
50. 10.1021/bm900842d10.1021/bm900842d ↗
51. 10.1038/emboj.2011.28610.1038/emboj.2011.286 ↗
52. 10.1002/anie.20090267210.1002/anie.200902672 ↗
53. 10.1163/092050610x48932110.1163/092050610x489321 ↗
54. 10.1002/jbm.a.3485310.1002/jbm.a.34853 ↗
55. 10.1021/acs.biomac.9b0165610.1021/acs.biomac.9b01656 ↗
56. 10.1016/j.nantod.2014.04.01110.1016/j.nantod.2014.04.011 ↗
57. 10.1093/emboj/20.6.132010.1093/emboj/20.6.1320 ↗
58. 10.1021/nn304949410.1021/nn3049494 ↗
59. 10.1016/j.jconrel.2012.09.01910.1016/j.jconrel.2012.09.019 ↗
60. 10.1039/c4tb02065k10.1039/c4tb02065k ↗
61. 10.1016/s0142-9612(02)00445-310.1016/s0142-9612(02)00445-3 ↗
62. 10.1016/s0168-3659(03)00076-210.1016/s0168-3659(03)00076-2 ↗
63. 10.1016/s0168-3659(01)00547-810.1016/s0168-3659(01)00547-8 ↗
64. 10.1073/pnas.070388210410.1073/pnas.0703882104 ↗
65. 10.1038/nbt.160210.1038/nbt.1602 ↗
66. 10.1073/pnas.130652911010.1073/pnas.1306529110 ↗
67. 10.1002/anie.20120326310.1002/anie.201203263 ↗
68. 10.1038/ncomms527710.1038/ncomms5277 ↗
69. 10.1016/j.jconrel.2010.11.00410.1016/j.jconrel.2010.11.004 ↗
70. Behr J.-P. · Chimia · 1997 · 51 · 3410.2533/chimia.1997.34 ↗