메뉴 건너뛰기




Volumn 122, Issue 9, 2000, Pages 1883-1890

Design of an oligosaccharide scaffold that binds in the minor groove of DNA

Author keywords

[No Author keywords available]

Indexed keywords

DOUBLE STRANDED DNA; OLIGOSACCHARIDE; PEPTIDE DERIVATIVE;

EID: 0034620783     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja992513f     Document Type: Article
Times cited : (54)

References (59)
  • 1
    • 0542421525 scopus 로고    scopus 로고
    • For a review of engineered biopolymers with well-defined folding properties, see: Gellman, S. Ace. Chem. Res. 1998, 31, 173-180.
    • (1998) Ace. Chem. Res. , vol.31 , pp. 173-180
    • Gellman, S.1
  • 25
    • 0028206164 scopus 로고
    • (b) The conformation of the trisaccharide portion of Aclacinomycin A is also consistent with this observation: Yang, D.; Wang, A. H. J. Biochemistry 1994,33,6595-6604.
    • (1994) Biochemistry , vol.33 , pp. 6595-6604
    • Yang, D.1    Wang, A.H.J.2
  • 27
  • 33
    • 0030684114 scopus 로고    scopus 로고
    • For other mechanistic studfes on the sulfoxide reaction, see: (a) Crich, D.; Sun, S. J. Am. Chem. Soc. 1997,119, 11217-11223.
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 11217-11223
    • Crich, D.1    Sun, S.2
  • 36
    • 0342441360 scopus 로고    scopus 로고
    • Ph.D. Thesis, Princeton University
    • Smith, A. Ph.D. Thesis, Princeton University, 1997.
    • (1997)
    • Smith, A.1
  • 37
    • 33847563666 scopus 로고    scopus 로고
    • This result suggests that the primary pathway for polymerization of these substrates involves activation of the anomeric sulfide with phenylsulfenyl Inflate (Pathway 2, Scheme 2)
    • This result suggests that the primary pathway for polymerization of these substrates involves activation of the anomeric sulfide with phenylsulfenyl Inflate (Pathway 2, Scheme 2).
  • 41
    • 0018707219 scopus 로고
    • This DNA sequence has been well-characterized by NMR: (a) Patel, D. J. Eur. J. Biochem. 1979, 99, 369-378.
    • (1979) Eur. J. Biochem. , vol.99 , pp. 369-378
    • Patel, D.J.1
  • 44
    • 0028303273 scopus 로고
    • An internally AT-rich DNA sequence was chosen since it has been shown that arginine residues in peptides prefer AT regions in DNA: Geierstanger, B. H.; Volkman, B. F.; Kremer, W.; Wemmer, D. E. Biochemistry 1994, 33, 5347-5355.
    • (1994) Biochemistry , vol.33 , pp. 5347-5355
    • Geierstanger, B.H.1    Volkman, B.F.2    Kremer, W.3    Wemmer, D.E.4
  • 58
    • 33847546612 scopus 로고    scopus 로고
    • Indirect chemical referencing was done using chemical shift referencing ratios obtained from the following: www.bmrb.\visc.edu/ref_info/cshift.html
  • 59
    • 33847562114 scopus 로고    scopus 로고
    • Assignments are reported to ±0.005 ppm accuracy. For the internal sugars B, C, and D overlap of resonances upon complexation to DNA made it difficult to measure chemical shift changes
    • Assignments are reported to ±0.005 ppm accuracy. For the internal sugars B, C, and D overlap of resonances upon complexation to DNA made it difficult to measure chemical shift changes.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.