CHARACTERIZATION of PEPTIDE NUCLEIC ACID AND COMPLEMENTARY DNA BY CAPILLARY ELECTROPHORESIS Xiaoqian WANG, Feng QU* School of Life Science, Beijing Institute of Technology, Beijing 100081,China Peptide nucleic acid (PNA) is a nucleic acid analogue, in which the pentose phosphate backbone in nucleic acid is replaced by a neutral peptide chain of N-(2 – aminoethyl) glycine. PNA can not be degraded by protease and nuclease. PNA has a high specificity and affinity when hybridizing with complementary DNA or RNA, and the hybridization is not influenced by solution and ionic condition [1] . As a modified nucleic acid, PNA may be used for protein recognition which is similar to aptamer. 15mer human thrombin aptamer is known to specifically recognize and stably combine human thrombin. In our work, the PNA which has the same base sequences with 15 mer aptamer was used. The investigation of PNA, 15 mer aptamer and its complementary DNA was done by capillary electrophoresis and nonaqueous capillary electrophoresis, the establishment of analytical methods will lay the foundation of molecule recognition and interaction studies of PNA, aptamer and their targets. REFERENCE 1. Shabih Shakeel, Sajjad Karim, Arif Ali. Peptide nucleic acid (PNA) – a review [J]. Journal of Chemical Technology and Biotechnology, 2006, 81: 892-899. ACKNOWLEDGEMENT The National Natural Science Foundation of China (No. 21135008、21175011、20875009). * Corresponding author: Prof. Feng Qu, E-mail: qufengqu@bit.edu.cn
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