A Quantum Dot Conjugated Sugar Ball and Its Cellular Uptake. On the Size Effects of Endocytosis in the Subviral RegionFumio Osaki, Takuya Kanamori, Shinsuke Sando et al.|Journal of the American Chemical Society|2004 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 approximately 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.
Helical Coordination Polymers from Achiral Components in Crystals. Homochiral Crystallization, Homochiral Helix Winding in the Solid State, and Chirality Control by SeedingTakayoshi Ezuhara, Ken Endo, Yasuhiro Aoyama|Journal of the American Chemical Society|1999 An achiral anthracene−pyrimidine derivative (5-(9-anthracenyl)pyrimidine, 1) forms adduct 1·Cd(NO3)2·H2O·EtOH (2) in chiral space group P21. The metal ion is hexacoordinated with two pyrimidine ligands (equatorial cis), water and ethanol (equatorial cis), and two nitrate ions (axial trans). The chirality arises from a pyrimidine−Cd2+ helical array and is preserved not only in each crystal via homochiral interstrand water−nitrate hydrogen bonding but also in all the crystals in the same chirality as a result of single-colony homochiral crystal growth. Compound 1 also forms achiral (Pbca) trihydrate adduct 1·Cd(NO3)2·3H2O (3) having nonhelical pyrimidine−Cd2+ zigzag chains. Achiral zigzag polymer 3 and chiral helical polymer 2 are interconvertible with each other in the solid states upon exchange of volatile ligands (ethanol and water). The helix winding associated with the conversion of adduct 3 to 2 can be made homochiral by seeding.
Molecular recognition. 5. Molecular recognition of sugars via hydrogen-bonding interaction with a synthetic polyhydroxy macrocycleYasuhiro Aoyama, Yasutaka Tanaka, Shuji Sugahara|Journal of the American Chemical Society|1989 ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTMolecular recognition. 5. Molecular recognition of sugars via hydrogen-bonding interaction with a synthetic polyhydroxy macrocycleYasuhiro Aoyama, Yasutaka Tanaka, and Shuji SugaharaCite this: J. Am. Chem. Soc. 1989, 111, 14, 5397–5404Publication Date (Print):July 1, 1989Publication History Published online1 May 2002Published inissue 1 July 1989https://pubs.acs.org/doi/10.1021/ja00196a052https://doi.org/10.1021/ja00196a052research-articleACS PublicationsRequest reuse permissionsArticle Views1401Altmetric-Citations292LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose Get e-Alerts
Guest-Binding Properties of Organic Crystals Having an Extensive Hydrogen-Bonded Network: An Orthogonal Anthracene-Bis(resorcinol) Derivative as a Functional Organic Analog of ZeolitesKen Endo, Tomoya Sawaki, Masayuki Koyanagi et al.|Journal of the American Chemical Society|1995 ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTGuest-Binding Properties of Organic Crystals Having an Extensive Hydrogen-Bonded Network: An Orthogonal Anthracene-Bis(resorcinol) Derivative as a Functional Organic Analog of ZeolitesKen Endo, Tomoya Sawaki, Masayuki Koyanagi, Kenji Kobayashi, Hideki Masuda, and Yasuhiro AoyamaCite this: J. Am. Chem. Soc. 1995, 117, 32, 8341–8352Publication Date (Print):August 1, 1995Publication History Published online1 May 2002Published inissue 1 August 1995https://doi.org/10.1021/ja00137a007RIGHTS & PERMISSIONSArticle Views851Altmetric-Citations189LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InReddit PDF (3 MB) Get e-AlertsSupporting Info (2)»Supporting Information Supporting Information Get e-Alerts
Artificial Viruses and Their Application to Gene Delivery. Size-Controlled Gene Coating with Glycocluster NanoparticlesYasuhiro Aoyama, Takuya Kanamori, Takashi Nakai et al.|Journal of the American Chemical Society|2003 Number- and size-controlled macromolecular associations are common in biology with viruses as a typical example. We report here a novel example of artificial viruses, in which the double-helical DNA is coated with 4-nm sized neutral glycocluster nanoparticles (GNPs) with a coating stoichiometry of approximately 2 GNPs per helical pitch (10 base pairs), where GNP arises from micellization of a cone-shaped, quadruple-chain glycocluster amphiphile having eight saccharide moieties with beta-glucoside termini on the calix[4]resorcarene macrocycle. The resulting "glycoviruses" are compactly packed (54 nm in the case of 7040 base-pair plasmid pCMVluc), are well charge-shielded (zeta congruent with approximately 0 mV), and effectively transfect cell cultures without notable cytotoxicity. The use of artificial viral vectors thus allows a new (nonamine/noncationic/nonpolymeric) access to gene delivery, a potential but still tough subject which has been studied extensively over the last 15 years by using viral or amine-based cationic vectors. The remarkable adhesion-manipulation ability of saccharide clusters also provides a strategy of bottom-up construction of nanometric or mesoscopic sizes.