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DTSTAMP:20240514T222324Z
UID:DEC44992-4EB0-4835-85E5-1627BFF88C91
DTSTART;TZID=Europe/Skopje:20240514T180000
DTEND;TZID=Europe/Skopje:20240514T193000
DESCRIPTION:Bottom-up self-assembly of DNA nanostructures have been propose
 d for variety of biotech uses ranging from information storage\, to target
 ed drug delivery or scaffolding for new materials. Engineering predefined 
 building blocks at nano level with various chiralities that assemble in la
 rge 3D crystallographic structures is an essential step for both 3D algori
 thmic assemblies as well as for spatial information storage. We will discu
 ss some recent developments in the field and will focus on spatial systems
  as models for information processing at molecular level. The rationally-d
 esigned 3D DNA motif\, the tensegrity triangle\, is the first DNA molecule
  used to provide DNA crystallographic assemblies. The possibilities of the
 se building blocks give ever-increasing geometric complexities that form v
 ast arrays of three-dimensional structures. We show a model that explains 
 and predicts which tensegrity triangle structures can form and which chira
 l topology they can form\, left- or right-handed. The theoretical model is
  also experimentally verified through units designed with incremental rota
 tional steps.\n\nSpeaker(s): Prof. Natasha Jonoska\, PhD\, \n\nUniversity 
 Ss. Cyril and Methodius\, Faculty of Computer Science and Engineering\, Ru
 dzer Boshkovikj 16\, Skopje\, Macedonia\, Macedonia\, 1000
LOCATION:University Ss. Cyril and Methodius\, Faculty of Computer Science a
 nd Engineering\, Rudzer Boshkovikj 16\, Skopje\, Macedonia\, Macedonia\, 1
 000
ORGANIZER:anastas.mishev@finki.ukim.mk
SEQUENCE:15
SUMMARY:Invited Lecture: DNA self-assembly and DNA nanotechnology 
URL;VALUE=URI:https://events.vtools.ieee.org/m/420575
X-ALT-DESC:Description: &lt;br /&gt;&lt;div&gt;\n&lt;p&gt;Bottom-up self-assembly of DNA nano
 structures have been proposed for variety of biotech uses ranging from inf
 ormation storage\, to targeted drug delivery or scaffolding for new materi
 als. Engineering predefined building blocks at nano level with various chi
 ralities that assemble in large 3D crystallographic structures is an essen
 tial step for both 3D algorithmic assemblies as well as for spatial inform
 ation storage. &amp;nbsp\;We will discuss some recent developments in the fiel
 d and will focus on spatial systems as models for information processing a
 t molecular level. The rationally-designed 3D DNA motif\, the tensegrity t
 riangle\, is the first DNA molecule used to provide DNA crystallographic a
 ssemblies. The &amp;nbsp\;possibilities of these building blocks give ever-inc
 reasing geometric complexities that form vast arrays of three-dimensional 
 structures. We show a model that explains and predicts which tensegrity tr
 iangle structures can form and which chiral topology they can form\, left-
  or right-handed. The theoretical model is also experimentally verified th
 rough units designed with incremental rotational steps.&lt;/p&gt;\n&lt;/div&gt;\n&lt;div&gt;
 &amp;nbsp\;&lt;/div&gt;
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