M
Mark A. Jarosinski
Researcher at Indiana University
Publications - 42
Citations - 4877
Mark A. Jarosinski is an academic researcher from Indiana University. The author has contributed to research in topics: Enantioselective synthesis & Receptor. The author has an hindex of 16, co-authored 40 publications receiving 4625 citations. Previous affiliations of Mark A. Jarosinski include University of Arizona & Amgen.
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Journal ArticleDOI
Beta-secretase cleavage of Alzheimer's amyloid precursor protein by the transmembrane aspartic protease BACE.
Robert Vassar,Brian D. Bennett,Safura Babu-Khan,Steve Kahn,Elizabeth A. Mendiaz,Paul Denis,David B. Teplow,Sandra Ross,Patricia Amarante,Richard Loeloff,Yi Luo,Seth Fisher,Janis Fuller,Steven P. Edenson,Jackson Lile,Mark A. Jarosinski,Anja Leona Biere,Eileen Curran,Teresa L. Burgess,Jean Claude Louis,Frank H. Collins,James J. S. Treanor,Gary Rogers,Martin Citron +23 more
TL;DR: Overexpression of a transmembrane aspartic protease, termed BACE (for beta-site APP-cleaving enzyme) increased the amount of beta-secretase cleavage products, and these were cleaved exactly and only at known beta- secretase positions.
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Parkinson's Disease-associated α-Synuclein Is More Fibrillogenic than β- and γ-Synuclein and Cannot Cross-seed Its Homologs
Anja Leona Biere,Stephen J. Wood,Jette Wypych,Shirley Steavenson,Yijia Jiang,Dan Anafi,Frederick W. Jacobsen,Mark A. Jarosinski,Gay-May Wu,Jean-Claude Louis,Francis Hall Martin,Linda O. Narhi,Martin Citron +12 more
TL;DR: β- and γ-synuclein are intrinsically less fibrillogenic than α- Synuclein and cannot form mixed fibrils with α- synuclein, which may explain why they do not appear in the pathological hallmarks of PD, although they are closely related to α-syn nuclein and are also abundant in brain.
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Structure of a human DNA repair protein UBA domain that interacts with HIV-1 Vpr.
Thorsten Dieckmann,Elizabeth S. Withers-Ward,Mark A. Jarosinski,Chuan-Fa Liu,Irvin S. Y. Chen,Juli Feigon +5 more
TL;DR: The HIV-1 protein Vpr is critical for a number of viral functions including a unique ability to arrest T-cells at a G2/M checkpoint and induce subsequent apoptosis and it has been shown to interact specifically with the second UBA (ubiquitin associated) domain found in the DNA repair protein HHR23A, a highly evolutionarily conserved protein.
Journal ArticleDOI
Structural and conformational requirements for high-affinity binding to the SH2 domain of Grb2(1).
Peter Ettmayer,John S. Gounarides,Mark A. Jarosinski,Mary-Sue Martin,Jean-Michel Rondeau,Michael Sabio,Sid Topiol,Beat Weidmann,Mauro Zurini,Kenneth W. Bair +9 more
TL;DR: These stable and easily accessible cyclic peptides can serve as templates for the evaluation of phosphotyrosine surrogates and further chemical elaboration and the potency of the authors' cyclic lactams can be explained by the stabilization of the beta-turn conformation by three intramolecular hydrogen bonds.
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Diastereospecific tandem Michael-like addition / electrophilic bromination: A one-pot tandem asymmetric synthesis of precursors of unusual amino acids
TL;DR: In this paper, a series of key intermediates of unusual β-methyl-amino acids have been synthesized by using a modified Evans auxiliary in an asymmetric Michael-like reaction followed by direct bromination in a one-pot reaction.