{"id":525,"date":"2021-08-14T11:31:51","date_gmt":"2021-08-14T02:31:51","guid":{"rendered":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/?page_id=525"},"modified":"2021-08-15T09:48:01","modified_gmt":"2021-08-15T00:48:01","slug":"synthesizing-dna-nucleic-acid-organic-chemistry","status":"publish","type":"page","link":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/synthesizing-dna-nucleic-acid-organic-chemistry\/","title":{"rendered":"Synthesizing DNA ~ Nucleic Acid Organic Chemistry"},"content":{"rendered":"\n<div class=\"wp-block-media-text alignwide has-media-on-the-right is-stacked-on-mobile\"><figure class=\"wp-block-media-text__media\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"768\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-content\/uploads\/sites\/62\/2021\/08\/IMG_4154-1024x768-1.jpg\" alt=\"\" class=\"wp-image-530 size-full\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-content\/uploads\/sites\/62\/2021\/08\/IMG_4154-1024x768-1.jpg 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-content\/uploads\/sites\/62\/2021\/08\/IMG_4154-1024x768-1-300x225.jpg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-content\/uploads\/sites\/62\/2021\/08\/IMG_4154-1024x768-1-768x576.jpg 768w, https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-content\/uploads\/sites\/62\/2021\/08\/IMG_4154-1024x768-1-660x495.jpg 660w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure><div class=\"wp-block-media-text__content\">\n<p>Our first key technology is <strong>nucleic acid organic chemistry<\/strong>, which uses the power of chemistry to &#8220;make&#8221; DNA as desired. Phosphoramidite chemistry enables sequential coupling of ATGC nucleotides in completely chemical process. Our advantage is that we can freely tune the process to suit our own preferences.<\/p>\n\n\n\n<p>By utilizing our knowledge of organic chemistry, which is taught in the classes, moreover, we can create reagents for writing yet unknown &#8220;characters&#8221; other than ATGC. While making full use of a wide variety of commercially available reagents, we have been creating <strong>molecular devices<\/strong> and <strong>machines<\/strong> with functions beyond those of nature by writing these unnatural &#8220;characters&#8221; into DNA using automatic DNA synthesizers. A typical example is the development of &#8220;<strong>molecular machine fluorescent probes<\/strong>,&#8221; which combine a fluorescent dye and a quencher through a mechanical coupling and operate with an unprecedented mechanism.<\/p>\n\n\n\n<p>\u2192Creating a diagnostic agent<\/p>\n<\/div><\/div>\n\n\n\n<p>The fact that we can freely synthesize DNA is a major advantage that differentiates us from other research groups competing on the world stage.<\/p>\n\n\n\n<p>\u2192Creating DDS carriers<br>\u2192Creating artificial antibodies<br>\u2192Creating molecular robots<\/p>\n\n\n\n<p>\u2192Creating artificial muscles<br>\u2192Producing artificial organs<\/p>\n\n\n\n<p>\u2192Go to &#8220;<a href=\"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/programming-dna-dna-computing-and-dna-nanotechnology\/\">Programming DNA<\/a>&#8220;<br>\u2192Back to &#8220;<a href=\"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/research-topics\/\">Research Topics<\/a>&#8220;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Our first key technology is nucleic acid organic chemistry, which uses the power of chemistry to &#8220;make&#8221; DNA as desired. Phosphoramidite chemistry enables sequential coupling of ATGC nucleotides in completely chemical process. Our advantage is that we can freely tune the process to suit our own preferences. By utilizing our knowledge of organic chemistry, which\u2026 <span class=\"read-more\"><a href=\"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/synthesizing-dna-nucleic-acid-organic-chemistry\/\">Read More &raquo;<\/a><\/span><\/p>\n","protected":false},"author":72,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-templates\/full-width.php","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"class_list":["post-525","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-json\/wp\/v2\/pages\/525","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-json\/wp\/v2\/users\/72"}],"replies":[{"embeddable":true,"href":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-json\/wp\/v2\/comments?post=525"}],"version-history":[{"count":7,"href":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-json\/wp\/v2\/pages\/525\/revisions"}],"predecessor-version":[{"id":568,"href":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-json\/wp\/v2\/pages\/525\/revisions\/568"}],"wp:attachment":[{"href":"https:\/\/wps.itc.kansai-u.ac.jp\/mol-mach2\/wp-json\/wp\/v2\/media?parent=525"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}