Structure-function correlation of chloroquine and analogues as transgene expression enhancers in nonviral gene delivery

Jianjun Cheng, Ryan Zeidan, Swaroop Mishra, Aijie Liu, Suzie H. Pun, Rajan P. Kulkarni, Gregory S. Jensen, Nathalie C. Bellocq, Mark E. Davis

Research output: Contribution to journalArticlepeer-review

109 Scopus citations


To understand how chloroquine (CQ) enhances transgene expression in polycation-based, nonviral gene delivery systems, a number of CQ analogues with variations in the aliphatic amino side chain or in the aromatic ring are synthesized and investigated. Our studies indicate that the aliphatic amino moiety of CQ is essential to provide increased gene expression. Further, the enhancements are more dramatically affected by changes to the aromatic ring and are positively correlated to the strength of intercalation between DNA and the CQ analogues. Quinacrine (QC), a CQ analogue with a fused acridinyl structure that can strongly intercalate DNA, enhances transfection similarly to CQ at a concentration 10 times lower, while N4-(4-pyridinyl)-N 1,N1-diethyl-1,4-pentanediamine (CP), a CQ analogue that has a weakly intercalating pyridinyl ring, shows no effect on gene expression. Subtle change on the 7-substituent of the chloroquine aromatic structure can also greatly affect the ability of the CQ analogues to enhance transgene expression. Transfection in the presence of N4-(7-trifluoromethyl-4- quinolinyl)-N1,N1-diethyl-1,4-pentanediamin e (CQ7a) shows expression efficiency 10 times higher than in the presence of CQ at-same concentration, while transfection in the presence of N4-(4- quinolinyl)-N1,N1-diethyl-1,4-pentanediamine (CQ7b) does not reveal any enhancing effects on expression. Through a number of comparative studies with CQ and its analogues, we conclude that there are at least three mechanistic features of CQ that lead to the enhancement in gene expression: (i) pH buffering in endocytic vesicles, (ii) displacement of polycations from the nucleic acids in polyplexes, and (iii) alteration of the biophysical properties of the released nucleic acid.

Original languageEnglish (US)
Pages (from-to)6522-6531
Number of pages10
JournalJournal of Medicinal Chemistry
Issue number22
StatePublished - Nov 2 2006
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Medicine
  • Drug Discovery


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