- Professor, University of Notre Dame
- Associate Professor, University of Notre Dame
- Assistant Professor, University of Notre Dame
- Postdoctoral Research Associate, Cornell University
- Ph.D. in Biochemistry, Michigan State University
- B.S. in Biochemistry, Albright College
- Fellow, Royal Society of Chemistry
- Fellow, American Chemical Society
- Fellow, American Association for the Advancement of Science
- Melville L. Wolfrom Award in Carbohydrate Chemistry, ACS Division of Carbohydrate Chemistry
- Kaneb Teaching Award
- John A. Boezi Memorial Alumnus Award, Michigan State University
- Horace S. Isbell Award in Carbohydrate Chemistry, ACS Division of Carbohydrate Chemistry
Professor Serianni's research focuses on the use of stable isotopically-labeled compounds to examine structure, conformation and reactivity of carbohydrates and nucleic acids in solution using modern multidimensional NMR methods and computational techniques. His group is interested in developing and improving chemical and chemi-enzymic methods to prepare carbohydrate-containing biomolecules containing one or more sites of isotopic enrichment, with 13C, 2H and 15N of primary concern. NMR studies of these labeled biomolecules permit a more detailed assessment of their 3-D structures in solution, information which is critical to understanding the fundamental factors controlling molecular recognition in biological processes.
Of current interest is the use of stable isotopes in the assessment of DNA and RNA structure in solution. Research is under way to: a) develop efficient chemical, chemi-enzymic, and/or biological methods to introduce isotopes selectively or uniformly into nucleosides and oligonucleotides, b) apply 2-D and 3-D NMR methods to decipher the NMR spectra of labeled oligonucleotides, and c) assess the merits of 13C-1H and 13C-13C spin-coupling constants within the furanose rings of RNA and DNA as structural probes. NMR data are complemented and extended by ab initio molecular orbital calculations which can assess the energetics and structural features of furanose ring pseudorotation and predict 13C-1H and 13C-13C spin-couplings for various pathways in these rings, and by X-ray crystallography. The long range objective is to apply this information to NMR solution studies of CCAAT-containing oligonucleotides involved in the NF-1 recognition site at the origin of replication of human adenovirus, and other biologically-important DNA and RNA oligomers.
Other work involves studies of carbohydrate metabolism via in vivo 13C and 19F NMR spectroscopy, and the development of automated devices for chemical and biological synthesis of labeled biomolecules.
- Meng, B.; Wang, J.; Wang, Q.; Serianni, A. S.; Pan, Q. "Rapid assembly of branched mannose oligosaccharides through consecutive regioselective glycosylation: A convergent and efficient strategy." Tetrahedron 2017, 73, 3932-3938.
- Zhang, W.; Turney, T.; Meredith, R.; Pan, Q.; Sernau, L.; Wang, X.; Hu, X.; Woods, R. J.; Carmichael, I.; Serianni, A. S. "Conformational Populations of beta-(1 -> 4) O-Glycosidic Linkages Using Redundant NMR J-Couplings and Circular Statistics." J. Phys. Chem. B 2017, 121, 3042-3058.
- Bose-Basu, B.; Zhang, W.; Kennedy, J. L. W.; Hadad, M. J.; Carmichael, I.; Serianni, A. S. "C-13-Labeled Idohexopyranosyl Rings: Effects of Methyl Glycosidation and C6 Oxidation on Ring Conformational Equilibria." J. Org. Chem. 2017, 82, 1356-1370.
- Turney, T.; Pan, Q.; Sernau, L.; Carmichael, I.; Zhang, W.; Wang, X.; Woods, R. J.; Serianni, A. S. "O-Acetyl Side-Chains in Monosaccharides: Redundant NMR Spin-Couplings and Statistical Models for Acetate Ester Conformational Analysis." J. Phys. Chem. B 2017, 121, 66-77.
- Zhang, W.; Zhao, S.; Serianni, A. S. "Labeling Monosaccharides With Stable Isotopes." Isotope Labeling of Biomolecules - Labeling Methods 2015, 565, 423-458
- Larson, D. J.; Middle, L.; Vu, H.; Zhang, W.; Serianni, A. S.; Duman, J.; Barnes, B. M. "Wood frog adaptations to overwintering in Alaska: new limits to freezing tolerance." J. Exp. Biol. 2014, 217, 2193-2200.