Nucleic acids research. Supplement (2001)最新文献

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Molecular recognition in P2 nucleotide receptors. P2核苷酸受体的分子识别。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.3
Kenneth A Jacobson
{"title":"Molecular recognition in P2 nucleotide receptors.","authors":"Kenneth A Jacobson","doi":"10.1093/nass/3.1.3","DOIUrl":"https://doi.org/10.1093/nass/3.1.3","url":null,"abstract":"","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"3-4"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Reaction of nucleosides with 2-acetoxyethyl acetoxymethyl ether. 核苷与2-乙酰氧基乙基乙酰氧基甲基醚的反应。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.11
G Framski, A Manikowski, T Zandecki, J Boryski
{"title":"Reaction of nucleosides with 2-acetoxyethyl acetoxymethyl ether.","authors":"G Framski,&nbsp;A Manikowski,&nbsp;T Zandecki,&nbsp;J Boryski","doi":"10.1093/nass/3.1.11","DOIUrl":"https://doi.org/10.1093/nass/3.1.11","url":null,"abstract":"<p><p>Application of 2-acetoxyethyl acetoxymethyl ether as a model of peracylated sugars (e.g. 1,2,3,5-tetra-O-acetyl-beta-D-ribofuranose) is a convenient way to study the mechanism and sequence of glycosyl exchange reactions in the nucleoside chemistry.</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"11-2"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.11","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824172","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Synthetic study of cytosaminomycins using the intramolecular glycosylation as a key step. 以分子内糖基化为关键步骤合成胞胺霉素的研究。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.21
Hideyuki Sugimura
{"title":"Synthetic study of cytosaminomycins using the intramolecular glycosylation as a key step.","authors":"Hideyuki Sugimura","doi":"10.1093/nass/3.1.21","DOIUrl":"https://doi.org/10.1093/nass/3.1.21","url":null,"abstract":"<p><p>2',6'-Dideoxy-beta-D-hexopyranosyl pyrimidine nucleoside, which is a component of anticoccidal antibiotics--cytosaminomycins, was synthesized in a stereoselective manner via the intramolecular pyrimidine delivery method. Further glycosylaion of the 4'-position with a glycosyl fluoride gave the disaccharide nucleoside skeleton of the cytosaminomycins.</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"21-2"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.21","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824177","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Development for an efficient synthesis method of 2'-deoxyguanosine-C8 adducts with several amino/nitro-arenes. 氨基/硝基芳烃合成2′-脱氧鸟苷- c8加合物的高效方法。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.23
Takeji Takamura-Enya, Satoko Ishikawa, Masataka Mochizuki, Keiji Wakabayashi
{"title":"Development for an efficient synthesis method of 2'-deoxyguanosine-C8 adducts with several amino/nitro-arenes.","authors":"Takeji Takamura-Enya,&nbsp;Satoko Ishikawa,&nbsp;Masataka Mochizuki,&nbsp;Keiji Wakabayashi","doi":"10.1093/nass/3.1.23","DOIUrl":"https://doi.org/10.1093/nass/3.1.23","url":null,"abstract":"<p><p>Heterocyclic amines (HCAs) are mutagenic compounds present in cooked meat and fish, and some of them are known to be carcinogenic. DNA adduct formation is now believed to be the initial critical step for carcinogenesis. HCAs are metabolically activated to form predominantly 2'-deoxyguanosine-C8 adducts (dG-C8 adduct) where the exocyclic N atom of activated compounds are covalently bound to the C8 position of dG. In order to prepare a high yield of dG-C8 adducts with HCAs, we tried to adapt the Buchwald-Hartwig arylamination reaction using 8-bromo-dG derivatives and HCAs. With the combined use of xantphos and Cs2CO3, we successfully obtained coupling compound derived from a carcinogenic HCA, 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx) at a 97% yield. Subsequent deprotection may lead to authentic dG-C8 adducts of several HCAs.</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"23-4"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.23","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824178","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Biochemical detection of adenosine and cytidine ionization within RNA by interference analysis. 干扰法检测RNA中腺苷和胞苷的电离。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.229
Scott A Strobel, Fatima D Jones, Adegboyega K Oyelere, Sean P Ryder
{"title":"Biochemical detection of adenosine and cytidine ionization within RNA by interference analysis.","authors":"Scott A Strobel,&nbsp;Fatima D Jones,&nbsp;Adegboyega K Oyelere,&nbsp;Sean P Ryder","doi":"10.1093/nass/3.1.229","DOIUrl":"https://doi.org/10.1093/nass/3.1.229","url":null,"abstract":"<p><p>Perturbation of active site functional group pKas is an important strategy employed by protein enzymes to achieve catalysis. There is increasing evidence to indicate that RNAs also utilize functional group pKa perturbation for folding and reactivity. The two best candidates for a functionally relevant pKa perturbation are the N3 of C (pKa 4.2) and the N1 of A (pKa 3.5), either of which could be sufficiently raised to allow protonation near physiological pH. Here we report the synthesis and use of a series of alpha-phosphorothioate tagged cytidine and adenosine analogs whose altered pKas make it possible to efficiently detect functionally relevant protonation events by Nucleotide Analog Interference Mapping. This approach has been used to detect ionization events in several catalytic RNAs, including the group I intron, the Hepatitis Delta Virus (HDV), the hairpin and the Varkud Satellite (VS) ribozymes. The active site residue of the VS ribozyme appears to be ionized in the course of the reaction pathway, which may be indicative of a general acid or base mechanism for catalysis by this RNA.</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"229-30"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.229","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824276","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Destruction of quadruplex by proteins, and its biological implications in replication and telomere maintenance. 蛋白质对四重体的破坏及其在复制和端粒维持中的生物学意义。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.231
Yoshiaki Enokizono, Akimasa Matsugami, Seiichi Uesugi, Hirokazu Fukuda, Naoto Tsuchiya, Takashi Sugimura, Minako Nagao, Hitoshi Nakagama, Masato Katahira
{"title":"Destruction of quadruplex by proteins, and its biological implications in replication and telomere maintenance.","authors":"Yoshiaki Enokizono,&nbsp;Akimasa Matsugami,&nbsp;Seiichi Uesugi,&nbsp;Hirokazu Fukuda,&nbsp;Naoto Tsuchiya,&nbsp;Takashi Sugimura,&nbsp;Minako Nagao,&nbsp;Hitoshi Nakagama,&nbsp;Masato Katahira","doi":"10.1093/nass/3.1.231","DOIUrl":"https://doi.org/10.1093/nass/3.1.231","url":null,"abstract":"<p><p>The minisatellite DNA Pc-1 consists of tandem repeats of d(GGCAG). We previously reported that a d(GGCAG)n strand folds into an intramolecular quadruplex under physiological conditions and that during replication the progression of DNA polymerase is blocked by the quadruplex in vitro. Therefore, the formation of the quadruplex was supposed to be responsible for the hypermutable features of Pc-1. Then, we have identified proteins that bind to Pc-1, one of which is hnRNP A1. Here, we have demonstrated that hnRNP A1 destroys the quadruplex of Pc-1 on binding and abrogates the arrest of DNA polymerase at the repeat. Thus, hnRNP A1 functions as if it is a chaperon to assist Pc-1 DNA to form the proper folding suitable for replication. We have also found that hnRNP A1 and a related protein, hnRNP D, destroy the quadruplex of telomere DNA, which suggests the involvement of these proteins in telomere maintenance as DNA chaperons.</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"231-2"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.231","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824277","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Site-selective DNA hydrolysis by the combination of Ce(IV) and oligonucleotide bearing EDTA groups. Ce(IV)和EDTA寡核苷酸组合的位点选择性DNA水解。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.137
Hiroyuki Arishima, Masahito Yokoyama, Makoto Komiyama
{"title":"Site-selective DNA hydrolysis by the combination of Ce(IV) and oligonucleotide bearing EDTA groups.","authors":"Hiroyuki Arishima,&nbsp;Masahito Yokoyama,&nbsp;Makoto Komiyama","doi":"10.1093/nass/3.1.137","DOIUrl":"https://doi.org/10.1093/nass/3.1.137","url":null,"abstract":"<p><p>By using appropriately modified oligonucleotides, a gap-structure is formed in substrate DNA, and 2-6 ethylenediamine-N,N,N'-triacetate residues are placed near this gap. When these composites are treated with homogenous Ce(IV)/EDTA complex, the phosphodiester linkages in the gap-site are selectively hydrolyzed at much greater rates than achieved previously by using unmodified oligonucelotides.</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"137-8"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.137","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824480","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
2,6-Diaminonaphthyridine derivatives bind to a single nucleotide bulge in DNA. 2,6-二氨基萘啶衍生物与DNA中的单个核苷酸凸起结合。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.139
Hitoshi Suda, Shinya Hagihara, Akio Kobori, Kazuhiko Nakatani, Isao Saito
{"title":"2,6-Diaminonaphthyridine derivatives bind to a single nucleotide bulge in DNA.","authors":"Hitoshi Suda,&nbsp;Shinya Hagihara,&nbsp;Akio Kobori,&nbsp;Kazuhiko Nakatani,&nbsp;Isao Saito","doi":"10.1093/nass/3.1.139","DOIUrl":"https://doi.org/10.1093/nass/3.1.139","url":null,"abstract":"<p><p>2,6-Diamino-1,8-naphthyridine derivative (daNpt), which possesses hydrogen bonding groups in an alignment of donor-acceptor-acceptor-donor binds to a single nucleotide bulge in the duplex. The melting temperatures (Tm) of all duplexes containing a bulge were increased, especially for the cytosine (C) and thymine (T) bulges, in the presence of daNpt, whereas only a small increase of Tm was observed for the fully matched duplexes. It was suggested by pH dependency of Tm and UV spectra, that a protonation of daNpt should play an important role for the recognition of C and T bulges.</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"139-40"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.139","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824481","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Study on interaction of a cationic porphyrin with DNA. 阳离子卟啉与DNA相互作用的研究。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.189
Takako Ohyama, Aya Sasagawa, Norifumi Terui, Hajime Mita, Yasuhiko Yamamoto
{"title":"Study on interaction of a cationic porphyrin with DNA.","authors":"Takako Ohyama,&nbsp;Aya Sasagawa,&nbsp;Norifumi Terui,&nbsp;Hajime Mita,&nbsp;Yasuhiko Yamamoto","doi":"10.1093/nass/3.1.189","DOIUrl":"https://doi.org/10.1093/nass/3.1.189","url":null,"abstract":"<p><p>5,10,15,20-Tetra(N-methyl-pyridinium-4-yl)-21H,23H-porphyrin has shown to bind to the major groove of AT-rich DNA predominantly through electrostatic interaction between positively charged N-methyl pyridinium moieties of the porphyrin and negatively charged phosphodiester backbone. Solution structure of the complex between the porphyrin and a double-stranded DNA fragment has been inferred from the measurements of the mixing time-dependent intermolecular nuclear Overhauser effects (NOEs).</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"189-90"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.189","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824486","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of a probe DNA which accompanies color change on hybridization. 杂交过程中伴随颜色变化的探针DNA的研制。
Nucleic acids research. Supplement (2001) Pub Date : 2003-01-01 DOI: 10.1093/nass/3.1.143
Hiromu Kashida, Hiroyuki Asanuma, Makoto Komiyama
{"title":"Development of a probe DNA which accompanies color change on hybridization.","authors":"Hiromu Kashida,&nbsp;Hiroyuki Asanuma,&nbsp;Makoto Komiyama","doi":"10.1093/nass/3.1.143","DOIUrl":"https://doi.org/10.1093/nass/3.1.143","url":null,"abstract":"<p><p>Naphthyl Red moiety, conjugated to DNA, shows distinct chromism by hybridization with its complementary DNA. Single-stranded DNA involving Naphthyl Red moiety exhibits orange color and has lambda max at 466 nm at pH 7.0. Absorption maximum shifts towards 545 nm by the presence of its complementary DNA, and accordingly color of the solution changes from orange to magenta.</p>","PeriodicalId":86149,"journal":{"name":"Nucleic acids research. Supplement (2001)","volume":" 3","pages":"143-4"},"PeriodicalIF":0.0,"publicationDate":"2003-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1093/nass/3.1.143","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40824655","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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