TY - JOUR
T1 - Nucleic acid junctions and lattices
AU - Seeman, Nadrian C.
N1 - Funding Information:
This work has been supported by a Basil O’Connor Starter Grant from The March of Dimes Birth Defects Foundation and Grants GM-26467 and GM-29554 from the NIH. I would like to thank Neville R. Kallenbach, Leonard S. Lerman, Bruce H. Robinson and RamaswamyH . Sarmaf or valuable discussionasn d invaluable encouragement.I would like to thank Ryland Loos and Robert Speck for assistancew ith the figures and Linda Welch for preparation of the manuscript. A preliminary account of this work was presenteda t the SecondC onversationi n the Discipline Biomolecular Stereodynamics,A lbany, New York, 26-29 April, 1981 .
PY - 1982/11/21
Y1 - 1982/11/21
N2 - It is possible to generate sequences of oligomeric nucleic acids which will preferentially associate to form migrationally immobile junctions, rather than linear duplexes, as they usually do. These structures are predicated on the maximization of Watson-Crick base pairing and the lack of sequence symmetry customarily found in their analogs in living systems. Criteria are presented which oligonucleotide sequences must fulfill in order to yield these junction structures. The generable junctions are nexi, from which 3 to 8 double helices may emanate. Each junction may be treated as a macromolecular "valence cluster", and the individual clusters may be linked together directly, or with pieces of linear DNA interspersed between them. This covalent linkage can be done with enormous specificity, using the sticky-ended ligation techniques currently employed in genetic engineering studies. It appears to be possible to generate covalently joined three-dimensional networks of nucleic acids which are periodic in connectivity and perhaps in space.
AB - It is possible to generate sequences of oligomeric nucleic acids which will preferentially associate to form migrationally immobile junctions, rather than linear duplexes, as they usually do. These structures are predicated on the maximization of Watson-Crick base pairing and the lack of sequence symmetry customarily found in their analogs in living systems. Criteria are presented which oligonucleotide sequences must fulfill in order to yield these junction structures. The generable junctions are nexi, from which 3 to 8 double helices may emanate. Each junction may be treated as a macromolecular "valence cluster", and the individual clusters may be linked together directly, or with pieces of linear DNA interspersed between them. This covalent linkage can be done with enormous specificity, using the sticky-ended ligation techniques currently employed in genetic engineering studies. It appears to be possible to generate covalently joined three-dimensional networks of nucleic acids which are periodic in connectivity and perhaps in space.
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U2 - 10.1016/0022-5193(82)90002-9
DO - 10.1016/0022-5193(82)90002-9
M3 - Article
C2 - 6188926
AN - SCOPUS:0020373595
SN - 0022-5193
VL - 99
SP - 237
EP - 247
JO - Journal of Theoretical Biology
JF - Journal of Theoretical Biology
IS - 2
ER -