Bioinformatics Vol. 17 no. 90001 2001
Pages S253-S261
© 2001 Oxford University Press
Designing better phages
Applied Algorithm Laboratory, Dept. of Computer Science, State University of New York, Stony Brook, NY, 11794-4400, USA
Received on February 5, 2001
; revised on March 30, 2001
; accepted on March 30, 2001
We propose a method to engineer the genome of bacteriophages to increase their effectiveness as antibacterial agents. Specifically, we exploit the redundancy of the triplet code to design genomes that avoid restriction sites while producing the same proteins as wild-type phages. We give an efficient algorithm to minimize the number of restriction sites against sets of cutter sequences, and demonstrate that that phage genomes can be significantly protected against surprisingly large sets of enzymes with no loss of function. Finally, we develop a model to explain why evolution has failed to eliminate many possible restriction sites despite selective pressure, thus motivating the need for genome-level sequence engineering.
Contact: skiena{at}cs.sunysb.edu
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Gavish, A. Peled, and B. Chor Genetic code symmetry and efficient design of GC-constrained coding sequences Bioinformatics, January 15, 2007; 23(2): e57 - e63. [Abstract] [Full Text] [PDF] |
||||
