TY - JOUR
T1 - Biomimetics
T2 - From bioinformatics to rational design of dendrimers as gene carriers
AU - Márquez-Miranda, Valeria
AU - Camarada, María Belén
AU - Araya-Durán, Ingrid
AU - Varas-Concha, Ignacio
AU - Almonacid, Daniel Eduardo
AU - González-Nilo, Fernando Danilo
N1 - Funding Information:
M.B.C. is grateful to Fondecyt for financial support (Initiation Project n° 11140107). V.M.M. thanks Conicyt for a PhD Scholarship and Conicyt + PAI “Concurso Nacional Tesis de Doctorado en la Empresa” 2014 (781413007). D.G.N., V.M.M. and I.A.D. thank the support of Fraunhofer Chile Research, Innova-Chile CORFO (FCR-CSB 09CEII-6991) and Anillo Científico ACT1107. The Centro Interdisciplinario de Neurociencia de Valparaíso (CINV) is a Millennium Institute supported by the Millennium Scientific Initiative of the Ministerio de Economía, Fomento y Turismo. The authors gratefully acknowledge Dr. Jeffrey Comer, from Kansas State University, for his valuable help in terms of scripts and design of figures.
Publisher Copyright:
© 2015 Márquez-Miranda et al.
PY - 2015/9/18
Y1 - 2015/9/18
N2 - Biomimetics, or the use of principles of Nature for developing new materials, is a paradigm that could help Nanomedicine tremendously. One of the current challenges in Nanomedicine is the rational design of new efficient and safer gene carriers. Poly(amidoamine) (PAMAM) dendrimers are a well-known class of nanoparticles, extensively used as nonviral nucleic acid carriers, due to their positively charged end-groups. Yet, there are still several aspects that can be improved for their successful application in in vitro and in vivo systems, including their affinity for nucleic acids as well as lowering their cytotoxicity. In the search of new functional groups that could be used as new dendrimer-reactive groups, we followed a biomimetic approach to determine the amino acids with highest prevalence in protein-DNA interactions. Then we introduced them individually as terminal groups of dendrimers, generating a new class of nanoparticles. Molecular dynamics studies of two systems: PAMAM-Arg and PAMAM-Lys were also performed in order to describe the formation of complexes with DNA. Results confirmed that the introduction of amino acids as terminal groups in a dendrimer increases their affinity for DNA and the interactions in the complexes were characterized at atomic level. We end up by briefly discussing additional modifications that can be made to PAMAM dendrimers to turned them into promising new gene carriers.
AB - Biomimetics, or the use of principles of Nature for developing new materials, is a paradigm that could help Nanomedicine tremendously. One of the current challenges in Nanomedicine is the rational design of new efficient and safer gene carriers. Poly(amidoamine) (PAMAM) dendrimers are a well-known class of nanoparticles, extensively used as nonviral nucleic acid carriers, due to their positively charged end-groups. Yet, there are still several aspects that can be improved for their successful application in in vitro and in vivo systems, including their affinity for nucleic acids as well as lowering their cytotoxicity. In the search of new functional groups that could be used as new dendrimer-reactive groups, we followed a biomimetic approach to determine the amino acids with highest prevalence in protein-DNA interactions. Then we introduced them individually as terminal groups of dendrimers, generating a new class of nanoparticles. Molecular dynamics studies of two systems: PAMAM-Arg and PAMAM-Lys were also performed in order to describe the formation of complexes with DNA. Results confirmed that the introduction of amino acids as terminal groups in a dendrimer increases their affinity for DNA and the interactions in the complexes were characterized at atomic level. We end up by briefly discussing additional modifications that can be made to PAMAM dendrimers to turned them into promising new gene carriers.
UR - http://www.scopus.com/inward/record.url?scp=84946742544&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0138392
DO - 10.1371/journal.pone.0138392
M3 - Article
AN - SCOPUS:84946742544
SN - 1932-6203
VL - 10
JO - PLoS ONE
JF - PLoS ONE
IS - 9
M1 - A1479
ER -