TY - JOUR
T1 - Rational design of a structural framework with potential use to develop chemical reagents that target and modulate multiple facets of Alzheimer's disease
AU - Lee, Sanghyun
AU - Zheng, Xueyun
AU - Krishnamoorthy, Janarthanan
AU - Savelieff, Masha G.
AU - Park, Hyun Min
AU - Brender, Jeffrey R.
AU - Kim, Jin Hoon
AU - Derrick, Jeffrey S.
AU - Kochi, Akiko
AU - Lee, Hyuck Jin
AU - Kim, Cheal
AU - Ramamoorthy, Ayyalusamy
AU - Bowers, Michael T.
AU - Lim, Mi Hee
PY - 2014/1/8
Y1 - 2014/1/8
N2 - Alzheimer's disease (AD) is characterized by multiple, intertwined pathological features, including amyloid-β (Aβ) aggregation, metal ion dyshomeostasis, and oxidative stress. We report a novel compound (ML) prototype of a rationally designed molecule obtained by integrating structural elements for Aβ aggregation control, metal chelation, reactive oxygen species (ROS) regulation, and antioxidant activity within a single molecule. Chemical, biochemical, ion mobility mass spectrometric, and NMR studies indicate that the compound ML targets metal-free and metal-bound Aβ (metal-Aβ) species, suppresses Aβ aggregation in vitro, and diminishes toxicity induced by Aβ and metal-treated Aβ in living cells. Comparison of ML to its structural moieties (i.e., 4-(dimethylamino)phenol (DAP) and (8-aminoquinolin-2-yl)methanol (1)) for reactivity with Aβ and metal-Aβ suggests the synergy of incorporating structural components for both metal chelation and Aβ interaction. Moreover, ML is water-soluble and potentially brain permeable, as well as regulates the formation and presence of free radicals. Overall, we demonstrate that a rational structure-based design strategy can generate a small molecule that can target and modulate multiple factors, providing a new tool to uncover and address AD complexity.
AB - Alzheimer's disease (AD) is characterized by multiple, intertwined pathological features, including amyloid-β (Aβ) aggregation, metal ion dyshomeostasis, and oxidative stress. We report a novel compound (ML) prototype of a rationally designed molecule obtained by integrating structural elements for Aβ aggregation control, metal chelation, reactive oxygen species (ROS) regulation, and antioxidant activity within a single molecule. Chemical, biochemical, ion mobility mass spectrometric, and NMR studies indicate that the compound ML targets metal-free and metal-bound Aβ (metal-Aβ) species, suppresses Aβ aggregation in vitro, and diminishes toxicity induced by Aβ and metal-treated Aβ in living cells. Comparison of ML to its structural moieties (i.e., 4-(dimethylamino)phenol (DAP) and (8-aminoquinolin-2-yl)methanol (1)) for reactivity with Aβ and metal-Aβ suggests the synergy of incorporating structural components for both metal chelation and Aβ interaction. Moreover, ML is water-soluble and potentially brain permeable, as well as regulates the formation and presence of free radicals. Overall, we demonstrate that a rational structure-based design strategy can generate a small molecule that can target and modulate multiple factors, providing a new tool to uncover and address AD complexity.
UR - https://www.scopus.com/pages/publications/84892177268
U2 - 10.1021/ja409801p
DO - 10.1021/ja409801p
M3 - Article
C2 - 24397771
AN - SCOPUS:84892177268
SN - 0002-7863
VL - 136
SP - 299
EP - 310
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 1
ER -