exonucleolytic sequencing;
DNA carrier particles;
immobilization;
dilution techniques;
fluorescent labelling;
D O I:
10.1016/S0168-1656(00)00419-3
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Different kinds of particles were investigated for their potential use as supports for exonucleolytic sequence analysis. Composite beads composed of an unreactive polystyrene 'core' and a 'shell' of functionalized silica nanoparticles were found to best fulfill the various prerequisites. The biotin/streptavidin system was used for attachment of DNA to composite beads of 6 mum diameter. Applying M13 ssDNA in extremely high dilution (similar to 1 molecule versus 100 beads) with internal fluorescent labels, only a small fraction of beads was found to be associated with fluorescent entities, which likely correspond to a very small number of bound DNA molecules per particle. For better selection and transfer of DNA-containing beads into microstructures for exonuclease degradation the loading experiments were repeated with composite beads of 2.3 mum diameter. In this case a covalent bond was formed between carboxylate-functionalized beads and amino-terminated oligonucleotides, which were detected through external labelling with fluorescent nanoparticles interacting with biotinylated segments of the complementary strand. (C) 2001 Published by Elsevier Science B.V.
机构:
University/Industry Chemical Research Center, Department of Chemistry, Mississippi State University, Mississippi State, MS 39762, United StatesUniversity/Industry Chemical Research Center, Department of Chemistry, Mississippi State University, Mississippi State, MS 39762, United States
机构:
University/Industry Chemical Research Center, Department of Chemistry, Mississippi State University, Mississippi State, MS 39762, United StatesUniversity/Industry Chemical Research Center, Department of Chemistry, Mississippi State University, Mississippi State, MS 39762, United States