TY - JOUR
T1 - Molecular engineering of somatostatin analogue with minimal dipeptide motif induces the formation of functional nanoparticles
AU - Shekhter Zahavi, Talia
AU - Oron-Herman, Mor
AU - Kostenich, Genady
AU - Rub, Eyal
AU - Salitra, Yoseph
AU - Buzhansky, Ludmila
AU - Orenstein, Arie
AU - Gazit, Ehud
AU - Adler-Abramovich, Lihi
N1 - Publisher Copyright:
© 2017 Wiley-VCH Verlag GmbH&Co. KGaA, Weinheim.
PY - 2017/1
Y1 - 2017/1
N2 - Functionalized nanoparticles decorated with functional biological entities serve as preferred vehicles for numerous theranostic applications. Here we offer an alternative strategy in which the targeting moieties also act as building blocks for the formation of functional nanoassemblies. Diphenylalanine, a small, highly potent self-assembling module, was incorporated with a somatostatin analogue, a modified hormone which preferentially binds to cancer cells. The co-assembly of the engineered hormone together with the structurally diverse diphenylalanine derivative allowed the formation of bioactive homogenous spherical nanostructures. Significant internalization capacity of the loaded co-assembled nanospheres into cancer cells in vitro, as well as selective in vivo accumulation in tumors, were demonstrated. These findings present a new method for the molecular engineering of bioactive peptide molecules by minor modifications with a remarkably potent association motif.
AB - Functionalized nanoparticles decorated with functional biological entities serve as preferred vehicles for numerous theranostic applications. Here we offer an alternative strategy in which the targeting moieties also act as building blocks for the formation of functional nanoassemblies. Diphenylalanine, a small, highly potent self-assembling module, was incorporated with a somatostatin analogue, a modified hormone which preferentially binds to cancer cells. The co-assembly of the engineered hormone together with the structurally diverse diphenylalanine derivative allowed the formation of bioactive homogenous spherical nanostructures. Significant internalization capacity of the loaded co-assembled nanospheres into cancer cells in vitro, as well as selective in vivo accumulation in tumors, were demonstrated. These findings present a new method for the molecular engineering of bioactive peptide molecules by minor modifications with a remarkably potent association motif.
KW - Co-assembly
KW - Nanocarriers
KW - Selfassembly
KW - Supramolecular chemistry
KW - Targeted drug delivery
UR - http://www.scopus.com/inward/record.url?scp=85028348233&partnerID=8YFLogxK
U2 - 10.1002/cnma.201600220
DO - 10.1002/cnma.201600220
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AN - SCOPUS:85028348233
SN - 2199-692X
VL - 3
SP - 27
EP - 32
JO - ChemNanoMat
JF - ChemNanoMat
IS - 1
ER -