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WFRF:(Jensen D. H.)
 

Sökning: WFRF:(Jensen D. H.) > (1995-1999) > Peptide nucleic aci...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00002870naa a2200373 4500
001oai:research.chalmers.se:2fcbfaeb-fb16-43d1-a833-8260cc46be26
003SwePub
008171007s1999 | |||||||||||000 ||eng|
024a https://research.chalmers.se/publication/1369562 URI
024a https://doi.org/10.1039/A902091H2 DOI
040 a (SwePub)cth
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Haaima, G.4 aut
2451 0a Peptide nucleic acids (PNA) derived from N-(N-methylaminoethyl)glycine. Synthesis, hybridization and structural properties
264 1c 1999
520 a Backbone N-methylated peptide nucleic acids (PNAs) containing the four nucleobases adenine, cytosine, guanine and thymine were synthesized via solid phase peptide oligomerization. The oligomers bind to their complementary target with a thermal stability that is 1.5-4.5 degrees C lower per "N-methyl nucleobase unit" [dependent on the number and position(s) of the N-methyl] than that of unmodified PNA. However, even fully N-methyl modified PNAs bind as efficiently to DNA or RNA targets as DNA itself. Furthermore, the hybridization efficiency per N-methyl unit in a PNA decreased with increasing N-methyl content, and the effect was more pronounced when the N-methyl backbone units are present in the Hoogsteen versus the Watson-Crick strand in (PNA)(2)-DNA triplexes. Interestingly, CD spectral analyses indicate that 30% (3 out of ten) substitution with N-methyl nucleobases did not alter the structure of PNA-DNA (or RNA) duplexes or (PNA)(2)-DNA triplexes, and likewise CD spectroscopy and X-ray crystallography showed no major structural differences between N-methylated (30%) and unmodified PNA-PNA duplexes. However, PNA-DNA duplexes as well as triplexes adopted a different conformation when formed with all-Ai-methyl PNAs.
650 7a NATURVETENSKAPx Kemix Fysikalisk kemi0 (SwePub)104022 hsv//swe
650 7a NATURAL SCIENCESx Chemical Sciencesx Physical Chemistry0 (SwePub)104022 hsv//eng
700a Rasmussen, H.4 aut
700a Schmidt, G.4 aut
700a Jensen, D.K.4 aut
700a Sandholm Kastrup, J.4 aut
700a Wittung Stafshede, Pernilla,d 1968u Chalmers tekniska högskola,Chalmers University of Technology4 aut0 (Swepub:cth)perwit
700a Nordén, Bengt,d 1945u Chalmers tekniska högskola,Chalmers University of Technology4 aut0 (Swepub:cth)norden
700a Buchardt, O.4 aut
700a Nielsen, P.E.4 aut
710a Chalmers tekniska högskola4 org
773t New Journal of Chemistryg 23:8, s. 833-840q 23:8<833-840x 1369-9261x 1144-0546
856u http://dx.doi.org/10.1039/A902091Hy FULLTEXT
8564 8u https://research.chalmers.se/publication/136956
8564 8u https://doi.org/10.1039/A902091H

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