Academic Health Center

Center for Drug Design

Swati S. More, PhD

AHCCDD2 - Content - Image - More - 180x222px

Academic Title

Assistant Professor

Education

Bachelor's
B. Tech Pharmaceuticals and Fine chemicals, University of Mumbai, India (1998-2002)
Ph.D.
Medicinal Chemistry, University of Minnesota, Minneapolis, MN (2002-2007)
Other Education
Postdoctoral Scholar, Department of Bioengineering and Therapeutic Sciences, University of California – San Francisco, San Francisco, CA (2007-2009); Research Associate, Center for Drug Design, University of Minnesota, Minneapolis, MN (2009-2012)

Contact Info

Email
morex002@umn.edu

Phone
612-626-1660

Fax
612-625-8154

Office Address

7-146 Phillips Wangensteen Building
516 Delaware Street SE
Minneapolis, MN-55455

Mailing Address

516 Delaware Street SE
MMC 204
Minneapolis, MN 55455   

More Group Research

Research Interests

Research in my laboratories seeks to identify, describe and solve biological problems through chemical means. Improved understanding of the molecular bases of various pathological and toxicological phenomena are regarded as milestones, with the design and successful development of novel chemical or biological therapeutics and diagnostic tools being the end-goals. A broad range of techniques are employed toward these ends, ranging from animal behavior studies, molecular biology, organic synthesis, rational drug design, biophysics, imaging and microscopy. A keen emphasis is placed on inculcating interdisciplinary research skills in laboratory personnel that would enable them to function as independent researchers.

 

Research Projects

Currently targeted areas are:

1. Oxidative stress – pathological and toxicological studies, chemoprevention, drug design.
Amyloidogenic peptides are established etiological agents of Alzheimer’s and Parkinson’s diseases. We have shown through biophysical and biochemical investigations that the food additive, 2,3-butanedione (diacetyl) is capable of inducing amyloid peptide misfolding in intact cells. Ongoing research seeks to define the relevance of this phenomenon in the intact animal.
The human body utilizes glutathione (1) as a primary cellular reductant. This thiol has been shown to be depleted in conditions of oxidative damage. Administration of 1 does not lead to the latter’s intact passage to the site of action due to metabolic breakdown by แตž-glutamyl transpeptidase. About five decades ago, Prof. Vince envisioned the creation of Ψ-GSH (2) as a means to bypass γ-glutamyl transpeptidase. We have now shown that 2 fulfills cardinal functions of 1, establishing it as a candidate for the treatment of a variety of conditions that involve deficiency of 1 and/or oxidative damage.

2. Drug transport – membrane transporters and their targeting.
The selective localization of membrane bound transport proteins renders attractive the latter’s exploitation for targeted drug delivery. Consequently, we are examining the distribution of membrane transporters in the body through various diagnostic probes and are designing small molecules that would be selectively uptaken by the transporter in question.

3. Imaging and diagnostic tool development.
We are seeking to validate imaging techniques for the identification and measurement of amyloidogenesis.

 

Publications

Recent Publications (For detailed publication list: (Click Here)

Vartak, A. P.; More, S. S.; Vince, R. Could the artificial butter flavoring, diacetyl, cause Alzheimer’s disease? Neurodegenerative Disease Management, 2012, 2: 1-3.

More, S. S.; Vartak, A. P.; Vince, R. Restoration of Glyoxalase Enzyme Activity Precludes Cognitive Dysfunction in a Mouse Model of Alzheimer’s Disease. ACS Chemical Neuroscience, 2013, 4: 330-8.

ahCCDD2 - Content - Image -Glyoxalase Scheme - 735px

More, S. S.; Vartak, A. P.; Vince, R. The Butter Flavorant, Diacetyl, Exacerbates β-Amyloid Cytotoxicity. Chemical Research in Toxicology, 2012, 25: 2083-91.

AHCCDD2-Image-Smore_TOCGraphic2_Border

Urscher, M.; More, S. S.; Alisch, R.; Vince, R.; Deponte, M. Tight-binding inhibitors efficiently inactivate both reaction centers of monomeric plasmodium falciparum glyoxalase 1. FEBS Journal, 2012, 279: 2568-78.

More, S. S.; Raza, A.; Vince, R. The Butter Flavorant, Diacetyl, Forms a Covalent Adduct with 2-Deoxyguanosine, Uncoils DNA and Leads to Cell Death. Journal of Agricultural and Food Chemistry, 2012, 60: 3311-17.

AHCCDD2-Image-Smore_TOCGraphic2_Border

More, S. S.; Vince, R. Potential of a γ-glutamyl-transpeptidase-stable glutathione analogue against amyloid-β toxicity. ACS Chemical Neuroscience, 2012, 3: 204-10.

More, S. S.; Itsara, M.; Yang, X.; Geier, E. G.; Tadano, M. K.; Seo, Y.; VanBrocklin, H. F.; Weiss, W. A.; Mueller, S.; Haas-Kogan, D. A.; DuBois, S. G.; Matthay, K. K.; Giacomini, K. M. Vorinostat increases expression of functional norepinephrine transporter in neuroblastoma in vitro and in vivo model systems. Clinical Cancer Research, 2011, 17: 2339-49.

Li, S.; Chen, Y.; Zhang, S.; More, S. S.; Huang, X.; Giacomini, KM. Role of Organic Cation Transporter 1, OCT1 in the Pharmacokinetics and Toxicity of cis-Diammine(pyridine)chloroplatinum(II) and Oxaliplatin in Mice. Pharmaceutical Research, 2011, 28: 610-25.

Chen, L.; Pawlikowski, B.; Schlessinger, A.; More, S. S.; Stryke, D.; Johns, S. J.; Portman, M. A.; Chen, E.; Ferrin, T. E.; Sali, A.; Giacomini, K. M. Role of organic cation transporter 3 (SLC22A3) and its missense variants in the pharmacologic action of metformin. Pharmacogenetics and Genomics, 2010, 20: 687-99.

  • ©2014 Regents of the University of Minnesota. All rights reserved.
  • The University of Minnesota is an equal opportunity educator and employer
  • Last modified on February 4, 2014