S
Stephen J. Hattan
Researcher at Applied Biosystems
Publications - 13
Citations - 5107
Stephen J. Hattan is an academic researcher from Applied Biosystems. The author has contributed to research in topics: Mass spectrometry & Matrix-assisted laser desorption/ionization. The author has an hindex of 8, co-authored 13 publications receiving 4889 citations. Previous affiliations of Stephen J. Hattan include University of New Hampshire.
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Journal ArticleDOI
Multiplexed Protein Quantitation in Saccharomyces cerevisiae Using Amine-reactive Isobaric Tagging Reagents
Philip L. Ross,Yulin N. Huang,Jason Marchese,Brian L. Williamson,Kenneth C. Parker,Stephen J. Hattan,Nikita Khainovski,Sasi Pillai,Subhakar Dey,Scott Daniels,Subhasish Purkayastha,Peter Juhasz,Stephen A. Martin,Michael Bartlet-Jones,Feng He,Allan Jacobson,Darryl J. Pappin,Darryl J. Pappin +17 more
TL;DR: It is found that inactivation of Upf1p and Xrn1p causes common as well as unique effects on protein expression, and the use of 4-fold multiplexing to enable relative protein measurements simultaneously with determination of absolute levels of a target protein using synthetic isobaric peptide standards.
Journal ArticleDOI
Detection of biomarkers with a multiplex quantitative proteomic platform in cerebrospinal fluid of patients with neurodegenerative disorders
Fadi A. Abdi,Joseph F. Quinn,Joseph Jankovic,Martin W. McIntosh,James B. Leverenz,Elaine R. Peskind,Randy Nixon,John G. Nutt,Katherine Chung,Cyrus P. Zabetian,Ali Samii,Melanie Lin,Stephen J. Hattan,Catherine Pan,Yan Wang,Jinghua Jin,David Zhu,G. Jane Li,Yan Liu,Dana Waichunas,Thomas J. Montine,Jing Zhang +21 more
TL;DR: The preliminary findings of iTRAQ suggest that a roster of proteins may be generated and developed into specific biomarkers that could eventually assist in clinical diagnosis and monitoring disease progression of AD, PD and DLB.
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Purification and Characterization of a Novel Calcium-binding Protein from the Extrapallial Fluid of the Mollusc, Mytilus edulis
TL;DR: Circular dichroism shows that the protein-calcium binding/protomer formation is coupled to a significant rearrangement in the protein's secondary structure in which there is a major reduction in β-sheet with an associated increase in α-helical content of the protein.
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Applications of MALDI Mass Spectrometry in Clinical Chemistry
TL;DR: There is substantial potential for MALDI-TOF MS to make further inroads into clinical chemistry because of the selectivity of mass detection and its ability to independently quantify proteoforms.
Journal ArticleDOI
Comparative study of [Three] LC-MALDI workflows for the analysis of complex proteomic samples.
TL;DR: The feasibility of MALDI MS/MS with off-line coupling to HPLC for the analysis of whole cell lysates of wild-type yeast by three different workflows is demonstrated and the effect of a workflow on the end results in terms of the number of proteins detected, the average peptide coverage of proteins, and thenumber of redundant peptide sequencing attempts is demonstrated.