Design of (Gd-DO3A)n-Polydiamidopropanoyl-Peptide Nucleic Acid-D(Cys-Ser-Lys-Cys) Magnetic Resonance Contrast Agents

被引:16
作者
Amirkhanov, Nariman V. [1 ,2 ]
Dimitrov, Ivan [3 ]
Opitz, Armin W. [4 ]
Zhang, Kaijun [5 ]
Lackey, John P. [5 ]
Cardi, Christopher A. [5 ]
Lai, Song [5 ]
Wagner, Norman J. [4 ]
Thakur, Mathew L. [5 ]
Wickstrom, Eric [1 ]
机构
[1] Thomas Jefferson Univ, Dept Biochem & Mol Biol, Philadelphia, PA 19107 USA
[2] Inst Chem Biol & Fundamental Med, Lab Nucle Acids Chem, Novosibirsk 630090, Russia
[3] Philips Med Syst, Cleveland, OH 44143 USA
[4] Univ Delaware, Ctr Mol & Engn Thermodynam, Dept Chem Engn, Newark, DE 19716 USA
[5] Thomas Jefferson Univ, Dept Radiol, Philadelphia, PA 19107 USA
关键词
chelator; dendrimer; hybridization; molecular imaging; noninvasive; oncogene; receptor; solid phase synthesis;
D O I
10.1002/bip.21059
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We hypothesized that chelating Gd(III) to 1,4,7-tris(carboxymethylaza)cyclododecane-10 -azaacetylamide (DO3A) on peptide nucleic acid (PNA) hybridization probes would provide a magnetic resonance genetic imaging agent capable of hybridization to a specific mRNA. Because of the low sensitivity of Gd(111) as an magnetic resonance imaging (MRI) contrast agent, a single Gd-DO3A complex per PNA hybridization agent could not provide enough contrast for detection of cancer gene mRNAs, even at thousands of mRNA copies per cell. To increase the Gd(111) shift intensity of MRI genetic imaging agents, we extended a novel DO3An-polydiamidopropanoyl (PDAP(111)) dendrimer, up to n = 16,from the N-terminus of KRAS PNA hybridization agents by solid phase synthesis. A C-terminal D(Cys-Ser-Lys-Cys) cyclized peptide analog of insulin-like growth factor 1 (IGF1) was included to enable receptor-mediated cellular uptake. Molecular dynamic simulation of the (Gd-DO3A-AEEA)(16)-PDAP(4)-AEEA(2)-KRAS PNA-AEEA-D(CYS-SCrLys-Cys) genetic imaging nanoparticles in explicit water yielded a pair correlation function similar to that of PAMAM dendrimers, and a predicted structure in which the PDAP dendron did not sequester the PNA. Thermal melting measurements indicated that the size of the PDAP dendron included in the (DO3A-AEEA)(n)-PDAP(m)-AEEA(2)-KRAS PNA-AEEA-D(Cys-Ser-Lys-Cys) probes (up to 16 Gd(III) cations per PNA) did not depress the melting temperatures (T-m) of the complementary PNA/RNA hybrid duplexes. The Gd(III) dendrimer PNA genetic imaging agents in phantom solutions displayed significantly greater T-1 relaxivity per probe (r(1) = 30.64 +/- 2.68 mM(-1) s(-1) for n = 2, r(1) = 153.84 +/- 11.28 mM(-1) s(-1) for n = 8) than Gd-DTPA (r(1) = 10.35 +/- 0.37 mM(-1) s(-1)), but less than that of (Gd-DO3A)(32)-PAMAM dendrimer (r(1) = 771.84 +/- 20.48 mM(-1) s(-1)) (P < 0.05). Higher generations of PDAP dendrimers with 32 or more Gd-DO3A residues attached to PNA-D(Cys-Ser-Lys-Cys) genetic imaging agents might provide greater contrast for more sensitive detection. (C) 2008 Wiley Periodicals, Inc. Biopolymers 89:1061-1076, 2008.
引用
收藏
页码:1061 / 1076
页数:16
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