抄録
The lipophilic CdSe quantum dot (QD) coated with trioctylphosphine oxide (TOPOQD) can be extracted from chloroform into water upon interaction with macrocyclic glycocluster amphiphile 1. The QD-conjugated and highly fluorescent sugar ball of a size of 15 nm (TOPOQD1) thus solubilized in water readily invades Hela cells via endocytosis. The endocytic activity of TOPOQD1 (15 nm), in light of those of the micellar homoaggregate of 1 (5 nm) and the virus-like 1-DNA conjugate (50 nm) as references, reveals a dramatic size effect (50 ≫15 ≫5) in the subviral size region. The optimal size at ∼50 nm indicates that size complementarity which governs molecular recognition in small host-guest systems also plays key roles in the encapsulation of nanometric guest particles by the endocytic vesicles (≤100 nm) as a macrobiomolecular host. The work thus suggests an utmost importance of size control at the viral size when designing molecular (gene, drug, probe, etc.) delivery machines.
本文言語 | English |
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ページ(範囲) | 6520-6521 |
ページ数 | 2 |
ジャーナル | Journal of the American Chemical Society |
巻 | 126 |
号 | 21 |
DOI | |
出版ステータス | Published - 6月 2 2004 |
外部発表 | はい |
ASJC Scopus subject areas
- 触媒
- 化学 (全般)
- 生化学
- コロイド化学および表面化学