Michael M. Marshall
University of North Carolina at Greensboro
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Publication
Featured researches published by Michael M. Marshall.
Scanning | 2012
Michael M. Marshall; Jijin Yang; Adam R. Hall
Helium ion milling of suspended silicon nitride thin films is explored. Milled squares patterned by scanning helium ion microscope are subsequently investigated by atomic force microscopy and the relation between ion dose and milling depth is measured for both the direct (side of ion incidence) and transmission (side opposite to ion incidence) regimes. We find that direct-milling depth varies linearly with beam dose while transmission-milling depth varies with the square of the beam dose, resulting in a straightforward method of controlling local film thickness.
Journal of Eukaryotic Microbiology | 2005
Parke A. Rublee; David L. Remington; Eric F. Schaefer; Michael M. Marshall
Abstract. Molecular methods, including conventional PCR, real‐time PCR, denaturing gradient gel electrophoresis, fluorescent fragment detection PCR, and fluorescent in situ hybridization, have all been developed for use in identifying and studying the distribution of the toxic dinoflagellates Pfiesteria piscicida and P. shumwayae. Application of the methods has demonstrated a worldwide distribution of both species and provided insight into their environmental tolerance range and temporal changes in distribution. Genetic variability among geographic locations generally appears low in rDNA genes, and detection of the organisms in ballast water is consistent with rapid dispersal or high gene flow among populations, but additional sequence data are needed to verify this hypothesis. The rapid development and application of these tools serves as a model for study of other microbial taxa and provides a basis for future development of tools that can simultaneously detect multiple targets.
Langmuir | 2015
Michael M. Marshall; Jan A. Ruzicka; Osama K. Zahid; Vincent C. Henrich; Ethan Will Taylor; Adam R. Hall
We study the binding of E. coli single-stranded binding protein (SSB) to single-stranded DNA (ssDNA) using a solid-state nanopore assay. We find that saturated nucleoprotein complexes can be distinguished easily from free SSB, ssDNA, or double-stranded DNA individually and demonstrate that the high affinity of SSB for ssDNA can be exploited to achieve high-fidelity differentiation from duplex molecules in a mixture. We then study nucleoprotein filament formation by systematically varying the amount of SSB relative to ssDNA. We observe a concomitant shift in the mean amplitude of electrical events that is consistent with weakly cooperative binding. Finally, we compare circular and linearized ssDNA saturated with SSB and use the results to infer structural details of the nucleoprotein complex.
PLOS ONE | 2014
Michael M. Marshall; Jan A. Ruzicka; Ethan Will Taylor; Adam R. Hall
Among the different types of DNA damage that occur endogenously in the cell, depurination is especially prevalent. These lesions can initiate mutagenesis and have been implicated in a variety of diseases, including cancer. Here, we demonstrate a new approach for the detection of depurination at the single-molecule scale using solid-state nanopores. We induce depurination in short duplex DNA using acidic conditions and observe that the presence of apurinic sites results in significantly slower dynamics during electrokinetic translocation. This procedure may be valuable as a diagnostic for in situ quantification of DNA depurination.
Archive | 2009
Parke A. Rublee; Vincent C. Henrich; Michael M. Marshall
Environmental assessment may be dramatically improved using a metagenomics approach directed at prokaryotic and eukaryotic microbes. These organisms respond rapidly to environmental change and are sensitive bioindicators, but fundamental knowledge of microbial biogeography is essential for valid environmental inferences to be made. Real-time quantitative PCR was used to determine if representative prokaryotic and eukaryotic taxa are widely dispersed across freshwater sites at narrow scales (regional, within a single state) to broad scales (comparisons among North American and Asian sites). The results demonstrate wide distribution of some taxa, but their abundance varies at individual sites presumably owing to local environmental conditions. Thus, direct assessments of abundance of targeted microbial consortia can be a tool for environmental monitoring and assessment.
Ecological Indicators | 2008
Michael M. Marshall; Rebecca N. Amos; Vincent C. Henrich; Parke A. Rublee
Archive | 2011
Parke A. Rublee; Vincent C. Henrich; Michael M. Marshall
Biophysical Journal | 2015
Michael M. Marshall; Jan A. Ruzicka; Osama K. Zahid; Ethan Will Taylor; Vincent C. Henrich; Adam R. Hall
Biophysical Journal | 2014
Michael M. Marshall; Vincent C. Henrich; Adam R. Hall
Biophysical Journal | 2013
Michael M. Marshall; Adam R. Hall