DNA ligands that bind tightly and selectively to cellobiose.

Cell surface oligosaccharides have been shown to play essential biological roles in such diverse biological phenomena as cellular adhesion, molecular recognition, and inflammatory response. The development of high-affinity ligands capable of selectively recognizing a variety of small motifs in different oligosaccharides would be of significant interest as experimental and diagnostic tools. As a step toward this goal we have developed DNA ligands that recognize the disaccharide cellobiose, whether in soluble form or as the repeating unit of the polymer, cellulose. These DNA "aptamers" bind with high selectivity to cellobiose with little or no affinity for the related disaccharides lactose, maltose, and gentiobiose. Thus, the DNA ligands can discriminate sugar epimers, anomers, and disaccharide linkages.

[1]  C. Glaudemans Mapping of subsites of monoclonal, anti-carbohydrate antibodies using deoxy and deoxyfluoro sugars , 1991 .

[2]  John M. Burke,et al.  In vitro selection and evolution of RNA: applications for catalytic RNA, molecular recognition, and drug discovery , 1993, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[3]  Y Wang,et al.  RNA molecules that specifically and stoichiometrically bind aminoglycoside antibiotics with high affinities. , 1996, Biochemistry.

[4]  D. Patel,et al.  Saccharide-RNA recognition in an aminoglycoside antibiotic-RNA aptamer complex. , 1997, Chemistry & biology.

[5]  M. Famulok,et al.  A novel RNA motif for neomycin recognition. , 1995, Chemistry & biology.

[6]  Nathan Sharon,et al.  The Lectins: Properties, Functions and Applications in Biology and Medicine , 1986 .

[7]  C. Tuerk,et al.  SELEXION. Systematic evolution of ligands by exponential enrichment with integrated optimization by non-linear analysis. , 1991, Journal of molecular biology.

[8]  A. Ellington,et al.  In vitro selection of RNA lectins: using combinatorial chemistry to interpret ribozyme evolution. , 1995, Chemistry & biology.

[9]  A. Pardi,et al.  High-resolution molecular discrimination by RNA. , 1994, Science.

[10]  Michael Famulok,et al.  Stereospecific recognition of tryptophan agarose by in vitro selected RNA , 1992 .

[11]  W. Weis,et al.  Structural basis of lectin-carbohydrate recognition. , 1996, Annual review of biochemistry.

[12]  G. F. Joyce,et al.  Amplification, mutation and selection of catalytic RNA. , 1989, Gene.

[13]  T. Cech,et al.  Monovalent cation-induced structure of telomeric DNA: The G-quartet model , 1989, Cell.

[14]  D. Engelke,et al.  Purification of Thermus aquaticus DNA polymerase expressed in Escherichia coli. , 1990, Analytical biochemistry.

[15]  P. Kováč,et al.  Binding of the O-antigen of Shigella dysenteriae type 1 and 26 related synthetic fragments to a monoclonal IgM antibody. , 1993, The Journal of biological chemistry.

[16]  L. Gold,et al.  Systematic evolution of ligands by exponential enrichment: RNA ligands to bacteriophage T4 DNA polymerase. , 1990, Science.

[17]  J. Szostak,et al.  Selection in vitro of single-stranded DNA molecules that fold into specific ligand-binding structures , 1992, Nature.

[18]  M Yarus,et al.  Diversity of oligonucleotide functions. , 1995, Annual review of biochemistry.

[19]  Michael R. Green,et al.  HIV-1 rev regulation involves recognition of non-Watson-Crick base pairs in viral RNA , 1991, Cell.

[20]  R. Rando,et al.  Specific binding of aminoglycoside antibiotics to RNA. , 1995, Chemistry & biology.

[21]  L. Gold,et al.  RNA pseudoknots that inhibit human immunodeficiency virus type 1 reverse transcriptase. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[22]  J. Szostak,et al.  In vitro selection of RNA molecules that bind specific ligands , 1990, Nature.

[23]  P. S. Kim,et al.  Bioactive and nuclease-resistant L-DNA ligand of vasopressin. , 1997, Proceedings of the National Academy of Sciences of the United States of America.