Fabrication of genetically engineered polypeptide@quantum dots hybrid nanogels for targeted imaging
Source abstract
Abstract
Nanogels have been widely used as multifunctional drug delivery carriers because of high water content, biocompatibility, and high loading capability. We designed and biosynthesized two triblock artificial polypeptides PC10A and PC10ARGD as vehicles for encapsulating hydrophobic materials. These polypeptides can form nanogels by self-assembly when the concentration is below 2% (w/v). The physical properties of nanogels, including size, surface potential, and targeting domain, are able to be tuned. Hydrophobic materials from molecular size to nano-size can be loaded into the polypeptide nanogels to form hybrid nanogels. Hydrophobic quantum dots CdSe@ZnS below 10 nM were loaded into the polypeptide nanogels by ultrasonic treatment. Encapsulation endows hydrophobic QDs with good tunability of size, water solubility, stability, targeting, and biocompatibility. PC10ARGD nanogels and PC10ARGD@QDs hybrid nanogels showed excellent biocompatibility, which the cellular viabilities of HeLa and MCF-7 cells treated with 1% PC10ARGD nanogels and PC10ARGD@QDs hybrid nanogels contained 20 nM QDs were above 90 and 80%, respectively. PC10ARGD@QDs hybrid nanogels with an arginine–glycine–aspartic acid motif present efficient receptor-mediated endocytosis in α v β 3 overexpressing HeLa cells but not in the control MCF-7 cells as analyzed by confocal microscopy. These results demonstrate that such polypeptide nanogels as nanocarriers are expected to have great potential applications in biomedicine.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Nanoparticle-Based Drug Delivery · Quantum Dots Synthesis And Properties · Advanced biosensing and bioanalysis techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (39)
Show source-provided references
1. Ali MR, Panikkanvalappil SR, El-Sayed MA (2014) Enhancing the efficiency of gold nanoparticles treatment of cancer by increasing their rate of endocytosis and cell accumulation using rifampicin. J Am Chem Soc 136:4464–4467. doi: 10.1021/ja412441210.1021/ja4124412 ↗
2. Chan WC, Nie S (1998) Quantum dot bioconjugates for ultrasensitive nonisotopic detection. Science 281:2016–2018. doi: 10.1126/science.281.5385.201610.1126/science.281.5385.2016 ↗
3. Chang E, Thekkek N, Yu WW et al (2006) Evaluation of quantum dot cytotoxicity based on intracellular uptake. Small 2:1412–1417. doi: 10.1002/smll.20060021810.1002/smll.200600218 ↗
4. Chen G, Tian F, Zhang Y et al (2014) Tracking of transplanted human mesenchymal stem cells in living mice using near-infrared Ag2S quantum dots. Adv Funct Mater 24:2481–2488. doi: 10.1002/adfm.20130326310.1002/adfm.201303263 ↗
5. Chen Y, Zheng M, Xiao Y et al (2016) A self-quenching-resistant carbon-dot powder with tunable solid-state fluorescence and construction of dual-fluorescence morphologies for white light-emission. Adv Mater 28:312–318. doi: 10.1002/adma.20150338010.1002/adma.201503380 ↗
6. Cheng X, Hinde E, Owen DM et al (2015) Enhancing quantum dots for bioimaging using advanced surface chemistry and advanced optical microscopy: application to silicon quantum dots (SiQDs). Adv Mater 27:6144–6150. doi: 10.1002/adma.20150322310.1002/adma.201503223 ↗
7. Davis ME, Chen Z, Shin DM (2008) Nanoparticle therapeutics: an emerging treatment modality for cancer. Nat Rev Drug Discov 7:771–782. doi: 10.1038/nrd261410.1038/nrd2614 ↗
8. Du C, Deng D, Shan L et al (2013) A pH-sensitive docorubicin prodrug based on folate-conjugated BSA for tumor-targeted drug delivery. Biomaterials 34:3087–3097. doi: 10.1016/j.biomaterials.2013.01.04110.1016/j.biomaterials.2013.01.041 ↗
9. Duxin N, Liu F, Vali H et al (2005) Cadmium sulphide quantum dots in morphologically tunable triblock copolymer aggregates. J Am Chem Soc 127:10063–10069. doi: 10.1021/ja050504310.1021/ja0505043 ↗
10. Ferji K, Hamouda I, Chassenieux C et al (2016) Fast and effective quantum-dots encapsulation and protection in PEO based photo-cross-linked micelles. J Colloid Interf Sci 476:222–229. doi: 10.1016/j.jcis.2016.05.03110.1016/j.jcis.2016.05.031 ↗
11. Gao X, Cui Y, Levenson RM et al (2004) In vivo cancer targeting and imaging with semiconductor quantum dots. Nat Biotechnol 22:969–976. doi: 10.1038/nbt99410.1038/nbt994 ↗
12. Gunasekar SK, Asnani M, Limbad C et al (2009) N-terminal aliphatic residues dictate the structure, stability, assembly, and small molecule binding of the coiled-coil region of cartilage oligomeric matrix protein. Biochemistry 48:8559–8567. doi: 10.1021/bi900534r10.1021/bi900534r ↗
13. Hines DA, Kamat PV (2013) Quantum dot surface chemistry: ligand effects and electron transfer reactions. J Phys Chem C 117:14418–14426. doi: 10.1021/jp404031s10.1021/jp404031s ↗
14. Kabanov AV, Vinogradov SV (2009) Nanogels as pharmaceutical carriers: finite networks of infinite capabilities. Angew Chem Int Ed 48:5418–5429. doi: 10.1002/anie.20090044110.1002/anie.200900441 ↗
15. Kang T, Um K, Park J et al (2016) Minimizing the fluorescence quenching caused by uncontrolled aggregation of CdSe/CdS core/shell quantum dots for biosensor applications. Sensor Actuat B-Chem 222:871–878. doi: 10.1016/j.snb.2015.09.03610.1016/j.snb.2015.09.036 ↗
16. Lee K, Rafi M, Wang X et al (2015) In vivo delivery of transcription factors with multifunctional oligonucleotides. Nat Mater 14:701–706. doi: 10.1038/NMAT426910.1038/NMAT4269 ↗
17. Li YL, Maciel D, Rodrigues J et al (2015a) Biodegradable polymer nanogels for drug/nucleic acid delivery. Chem Rev 115:8564–8608. doi: 10.1021/cr500131f10.1021/cr500131f ↗
18. Li ZB, Huang H, Tang SY et al (2015b) Small gold nanorods laden macrophages for enhanced tumor coverage in photothermal therapy. Biomaterials 74:144–154. doi: 10.1016/j.biomaterials.2015.09.03810.1016/j.biomaterials.2015.09.038 ↗
19. Liu B, Lewis AK, Shen W (2009) Physical hydrogels photo-cross-linked from self-assembled macromers for potential use in tissue engineering. Biomacromolecules 10:3182–3187. doi: 10.1021/bm900908g10.1021/bm900908g ↗
20. Mattoussi H, Palui G, Na HB (2012) Luminescent quantum dots as platforms for probing in vitro and in vivo biological processes. Adv Drug Deliv Rev 64:138–166. doi: 10.1016/j.addr.2011.09.01110.1016/j.addr.2011.09.011 ↗
21. Murray C, Norris DJ, Bawendi MG (1993) Synthesis and characterization of nearly monodisperse CdE (E = sulfur, selenium, tellurium) semiconductor nanocrystallites. J Am Chem Soc 115:8706–8715. doi: 10.1021/ja00072a02510.1021/ja00072a025 ↗
22. Oh E, Liu R, Nel A et al (2016) Meta-analysis of cellular toxicity for cadmium-containing quantum dots. Nat Nanotechnol 11:479–486. doi: 10.1038/NNANO.2015.33810.1038/NNANO.2015.338 ↗
23. Oun R, Floriano RS, Isaacs L et al (2014) The ex vivo neurotoxic, myotoxic and cardiotoxic activity of cucurbituril-based macrocyclic drug delivery vehicles. Toxicol Res 3:447–455. doi: 10.1039/c4tx00082j10.1039/c4tx00082j ↗
24. Park J, An K, Hwang Y et al (2004) Ultra-large-scale syntheses of monodisperse nanocrystals. Nat Mater 3:891–895. doi: 10.1038/nmat125110.1038/nmat1251 ↗
25. Purwada A, Tian YF, Huang WS et al (2016) Self-assembly protein nanogels for safer cancer immunotherapy. Adv Healthc Mater 5:1413–1419. doi: 10.1002/adhm.20150106210.1002/adhm.201501062 ↗
26. Reiss P, Protiere M, Li L (2009) Core/shell semiconductor nanocrystals. Small 5:154–168. doi: 10.1002/smll.20080084110.1002/smll.200800841 ↗
27. Sánchez-Paradinas S, Dorfs D, Friebe S et al (2015) Aerogels from CdSe/CdS nanorods with ultra-long exciton lifetimes and high fluorescence quantum yields. Adv Mater 27:6152–6156. doi: 10.1002/adma.20150207810.1002/adma.201502078 ↗
28. Shen W, Kornfield JA, Tirrell DA (2007) Dynamic properties of artificial protein hydrogels assembled through aggregation of leucine zipper peptide domains. Macromolecules 40:689–692. doi: 10.1021/ma061519410.1021/ma0615194 ↗
29. Shen W, Zhang K, Kornfield JA et al (2006) Tuning the erosion rate of artificial protein hydrogels through control of network topology. Nat Mater 5:153–158. doi: 10.1038/nmat157310.1038/nmat1573 ↗
30. Tyrakowski CM, Snee PT (2014) A primer on the synthesis, water-solubilization, and functionalization of quantum dots, their use as biological sensing agents, and present status. Phys Chem Chem Phys 16:837–855. doi: 10.1039/C3CP53502A10.1039/C3CP53502A ↗
31. Valizadeh A, Mikaeili H, Samiei M et al (2012) Quantum dots: synthesis, bioapplications, and toxicity. Nanoscale Res Lett 7:480. doi: 10.1186/1556-276X-7-48010.1186/1556-276X-7-480 ↗
32. Wu P, Zhao T, Wang SL et al (2014) Semiconductor quantum dots-based metal ion probes. Nano 6:43–64. doi: 10.1039/C3NR04628A10.1039/C3NR04628A ↗
33. Würth C, Grabolle M, Pauli J et al (2013) Relative and absolute determination of fluorescence quantum yields of transparent samples. Nat Protoc 8:1535–1550. doi: 10.1038/nprot.2013.08710.1038/nprot.2013.087 ↗
34. Yang J, Yao MH, Wen L et al (2014) Multifunctional quantum dot-polypeptide hybrid nanogel for targeted imaging and drug delivery. Nano 6:11282–11292. doi: 10.1039/c4nr03058c10.1039/c4nr03058c ↗
35. Yao MH, Yang J, Du MS et al (2014a) Polypeptide-engineered physical hydrogels designed from the coiled-coil region of cartilage oligomeric matrix protein for three-dimensional cell culture. J Mater Chem B 2:3123–3132. doi: 10.1039/C4TB00107A10.1039/C4TB00107A ↗
36. Yao MH, Yang J, Song JT et al (2014b) Directed self-assembly of polypeptide-engineered physical microgels for building porous cell-laden hydrogels. Chem Commun 50:9405–9408. doi: 10.1039/C4CC04018J10.1039/C4CC04018J ↗
37. Yong KT, Law WC, Hu R et al (2013) Nanotoxicity assessment of quantum dots: from cellular to primate studies. Chem Soc Rev 42:1236–1250. doi: 10.1039/c2cs35392j10.1039/c2cs35392j ↗
38. Zhang MZ, Yu RN, Chen J et al (2012) Targeted quantum dots fluorescence probes functionalized with aptamer and peptide for transferrin receptor on tumor cells. Nanotechnology 23:485104. doi: 10.1088/0957-4484/23/48/48510410.1088/0957-4484/23/48/485104 ↗
39. Zhou J, Yang Y, Zhang CY (2015) Toward biocompatible semiconductor quantum dots: from biosynthesis and bioconjugation to biomedical application. Chem Rev 115:11669–11717. doi: 10.1021/acs.chemrev.5b0004910.1021/acs.chemrev.5b00049 ↗