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Synthetic peptide nano-1 increases t...
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Chin, Shook-Fong.
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Synthetic peptide nano-1 increases the uptake of single-walled carbon nanotubes by HeLa cells.
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Synthetic peptide nano-1 increases the uptake of single-walled carbon nanotubes by HeLa cells./
作者:
Chin, Shook-Fong.
面頁冊數:
171 p.
附註:
Source: Dissertation Abstracts International, Volume: 66-05, Section: B, page: 2556.
Contained By:
Dissertation Abstracts International66-05B.
標題:
Chemistry, Analytical. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3176113
ISBN:
9780542147012
Synthetic peptide nano-1 increases the uptake of single-walled carbon nanotubes by HeLa cells.
Chin, Shook-Fong.
Synthetic peptide nano-1 increases the uptake of single-walled carbon nanotubes by HeLa cells.
- 171 p.
Source: Dissertation Abstracts International, Volume: 66-05, Section: B, page: 2556.
Thesis (Ph.D.)--The University of Texas at Dallas, 2005.
Numerous discoveries and procedures developed by the UTD BioNano Group with respect to the isolation and aqueous solubilization of single-walled carbon nanotubes have set the stage for their use in biomedical applications. The key ingredient in these works is a 29-amino acid residue peptide termed nano-1 that can coat carbon nanotubes. The work presented in this Fundamental Practicum describes the first experiments exposing mammalian cells to these coated nanotubes. First, the synthesis and characterization of dye-labeled nano-1 was achieved to permit confocal fluorescence microscopy of HeLa cells incubated with peptide-coated carbon nanotubes. Second, a modified sonication and centrifugation procedure was developed to enrich for shorter length (∼100-nm long) peptide-coated nanotubes to facilitate their entry into cells. Third, conditions whereby peptide, nanotubes, and peptide-coated nanotubes did not alter the growth characteristic of HeLa cells over the course of 4 days were determined. Fourth, Raman spectroscopy and confocal fluorescence microscopy were used to reveal that: (i) nanotubes (peptide-coated and non-coated) entered HeLa cells in a time- and metabolic-dependent fashion; (ii) that both peptide-coated and non-coated nanotubes could be detected in the cytoplasm and nucleus of cells; (iii) that higher relative ratios of uncoated nanotubes were distributed in the nucleus relative to the cytoplasm; (iv) that higher relative ratios of peptide-coated nanotubes were distributed in the cytoplasm relative to the nucleus; (v) that ∼3-fold more peptide-coated nanotubes entered the nucleus of HeLa cells relative to the non-coated nanotubes; and finally, (vi) that ∼8-fold more peptide-coated nanotubes entered the cytoplasm of HeLa cells relative to the non-coated nanotubes.
ISBN: 9780542147012Subjects--Topical Terms:
586156
Chemistry, Analytical.
Synthetic peptide nano-1 increases the uptake of single-walled carbon nanotubes by HeLa cells.
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Numerous discoveries and procedures developed by the UTD BioNano Group with respect to the isolation and aqueous solubilization of single-walled carbon nanotubes have set the stage for their use in biomedical applications. The key ingredient in these works is a 29-amino acid residue peptide termed nano-1 that can coat carbon nanotubes. The work presented in this Fundamental Practicum describes the first experiments exposing mammalian cells to these coated nanotubes. First, the synthesis and characterization of dye-labeled nano-1 was achieved to permit confocal fluorescence microscopy of HeLa cells incubated with peptide-coated carbon nanotubes. Second, a modified sonication and centrifugation procedure was developed to enrich for shorter length (∼100-nm long) peptide-coated nanotubes to facilitate their entry into cells. Third, conditions whereby peptide, nanotubes, and peptide-coated nanotubes did not alter the growth characteristic of HeLa cells over the course of 4 days were determined. Fourth, Raman spectroscopy and confocal fluorescence microscopy were used to reveal that: (i) nanotubes (peptide-coated and non-coated) entered HeLa cells in a time- and metabolic-dependent fashion; (ii) that both peptide-coated and non-coated nanotubes could be detected in the cytoplasm and nucleus of cells; (iii) that higher relative ratios of uncoated nanotubes were distributed in the nucleus relative to the cytoplasm; (iv) that higher relative ratios of peptide-coated nanotubes were distributed in the cytoplasm relative to the nucleus; (v) that ∼3-fold more peptide-coated nanotubes entered the nucleus of HeLa cells relative to the non-coated nanotubes; and finally, (vi) that ∼8-fold more peptide-coated nanotubes entered the cytoplasm of HeLa cells relative to the non-coated nanotubes.
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