journal article·2010-11-23

Tracking the Endocytic Pathway of Recombinant Protein Toxin Delivered by Multiwalled Carbon Nanotubes

Meiyan Wang, Shaoning Yu, Chuan Wang, Jilie Kong

ACS Nano· Volume 4· Issue 11
Publisher page

Abstract

The endocytic pathway of a recombinant protein toxin, ricin A-chain (RTA), delivered by multiwalled carbon nanotubes (MWCNTs) was tracked in HeLa cells by tagging RTA with enhanced green fluorescent protein (EGFP). EGFP-RTA was found to accumulate in the endosome and to be retrogradely transported to the endoplasmic reticulum, from which it translocated into the cytosol. Nuclear staining, Z-axis scanning with a laser scanning confocal microscope (LSCM), and transmission electron microscopy (TEM) indicated that the RTA exerted its toxic effects. Endocytosis-inhibiting tests with LSCM and flow cytometry showed that MWCNT-EGFP-RTA conjugates penetrated cells principally via clathrin-mediated endocytosis. These studies are beneficial to understanding the MWCNT-based intracellular drug delivery mechanism and provide guidelines for designing promising MWCNT-based vectors for targeting diagnostic or therapeutic compounds, not only to specific cells, but even to specific cellular compartments.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Toxin Mechanisms and Immunotoxins · Force Microscopy Techniques and Applications · Lipid Membrane Structure and Behavior

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

Affiliations

Department of Chemistry and Institutes of Biomedical Sciences, Fudan University, Shanghai, P.R. China

References (45)

Show source-provided references
1. Fitzgerald D. J. P. · Cell · 1983 · 32 · 60710.1016/0092-8674(83)90480-4 ↗
2. Pastan I. · Cell · 1986 · 47 · 64110.1016/0092-8674(86)90506-4 ↗
3. Johannes L. · Gene Ther. · 2005 · 12 · 136010.1038/sj.gt.3302557 ↗
4. Sandvig K. · Embo J. · 2000 · 19 · 594310.1093/emboj/19.22.5943 ↗
5. Jaffrezou J. P. · Cancer Res. · 1992 · 52 · 1352
6. Rapak A. · Proc. Natl. Acad. Sci. U.S.A. · 1997 · 94 · 378310.1073/pnas.94.8.3783 ↗
7. Sandvig K. · FEBS Lett. · 2002 · 529 · 4910.1016/S0014-5793(02)03182-4 ↗
8. Sandvig K. · Annu. Rev. Cell Dev. Biol. · 2002 · 18 · 110.1146/annurev.cellbio.18.011502.142107 ↗
9. Watson P. · Adv. Drug Delivery Rev. · 2006 · 58 · 158110.1016/j.addr.2006.09.016 ↗
10. Spooner R. A. · Curr. Opin. Drug Discovery Dev. · 2010 · 13 · 86
11. Kreitman R. J. · Curr. Opin. Mol. Ther. · 2003 · 5 · 44
12. Olsnes S. · Toxicon · 2004 · 44 · 36110.1016/j.toxicon.2004.05.003 ↗
13. Leshin J. · Toxicon · 2010 · 55 · 65810.1016/j.toxicon.2009.09.002 ↗
14. Pastan I. · Nat. Rev. Cancer · 2006 · 6 · 55910.1038/nrc1891 ↗
15. Baluna R. · Proc. Natl. Acad. Sci. U.S.A. · 1999 · 96 · 395710.1073/pnas.96.7.3957 ↗
16. Baluna R. · Exp. Cell Res. · 2000 · 258 · 41710.1006/excr.2000.4954 ↗
17. Sturm M. B. · J. Am. Chem. Soc. · 2007 · 129 · 554410.1021/ja068054h ↗
18. Kreitman R. J. · Nat. Biotechnol. · 2003 · 21 · 37210.1038/nbt0403-372 ↗
19. Cho K. J. · Clin. Cancer Res. · 2008 · 14 · 131010.1158/1078-0432.CCR-07-1441 ↗
20. Farokhzad O. C. · ACS Nano · 2009 · 3 · 1610.1021/nn900002m ↗
21. Pantarotto D. · Chem. Commun. · 2004 · 1610.1039/b311254c ↗
22. Kam N. W. S. · J. Am. Chem. Soc. · 2004 · 126 · 685010.1021/ja0486059 ↗
23. Kam N. W. S. · J. Am. Chem. Soc. · 2005 · 127 · 602110.1021/ja050062v ↗
24. Weng X. X. · Mol. Biosyst. · 2009 · 5 · 122410.1039/b906948h ↗
25. Liu Y. · Angew. Chem., Int. Ed. · 2005 · 44 · 478210.1002/anie.200500042 ↗
26. Cai D. · Nat. Methods · 2005 · 2 · 44910.1038/nmeth761 ↗
27. Bianco A. · Chem. Commun. · 2005 · 57110.1039/b410943k ↗
28. Allen T. M. · Science · 2004 · 303 · 181810.1126/science.1095833 ↗
29. Panhuis M. I. H. · Chem. Biol. · 2003 · 10 · 89710.1016/j.chembiol.2003.10.005 ↗
30. Qu G. B. · Carbon · 2009 · 47 · 206010.1016/j.carbon.2009.03.056 ↗
31. Liu Q. L. · Nano Lett. · 2009 · 9 · 100710.1021/nl803083u ↗
32. Kang S. · Langmuir · 2008 · 24 · 640910.1021/la800951v ↗
33. Kam N. W. S. · Angew. Chem., Int. Ed. · 2006 · 45 · 57710.1002/anie.200503389 ↗
34. Jin H. · Nano Lett. · 2008 · 8 · 157710.1021/nl072969s ↗
35. Jin H. · ACS Nano · 2009 · 3 · 14910.1021/nn800532m ↗
36. Kostarelos K. · Nat. Nanotechnol. · 2007 · 2 · 10810.1038/nnano.2006.209 ↗
37. Porter A. E. · Nat. Nanotechnol. · 2007 · 2 · 71310.1038/nnano.2007.347 ↗
38. Cherukuri P. · J. Am. Chem. Soc. · 2004 · 126 · 1563810.1021/ja0466311 ↗
39. Spooner R. A. · Proc. Natl. Acad. Sci. U.S.A. · 2008 · 105 · 1740810.1073/pnas.0809013105 ↗
40. Ludin B. · Gene · 1996 · 173 · 10710.1016/0378-1119(95)00899-3 ↗
41. Miyawaki A. · Cell Struct. Funct. · 2002 · 27 · 34310.1247/csf.27.343 ↗
42. Hartley M. R. · BBA-Proteins Proteomics · 2004 · 1701 · 110.1016/j.bbapap.2004.06.004 ↗
43. Roberts L. M. · Toxicon · 2004 · 44 · 46910.1016/j.toxicon.2004.07.002 ↗
44. Mayerhofer P. U. · J. Biol. Chem. · 2009 · 284 · 1023210.1074/jbc.M808387200 ↗
45. Xu Z. H. · Biomaterials · 2009 · 30 · 22610.1016/j.biomaterials.2008.09.014 ↗