Tara Little, Ph.D.

Tara Little, Ph.D.

Washington DC-Baltimore Area
988 followers 500 connections

About

I'm a researcher-turned-sales manager with a strong background in biochemical and…

Activity

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Experience

  • Proteintech Group Graphic

    Proteintech Group

    Mid-Atlantic

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    Gaithersburg, Maryland, United States

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    Frederick, Maryland

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    Frederick, MD

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    Frederick, MD

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Education

  • Johns Hopkins Bloomberg School of Public Health Graphic

    Johns Hopkins Bloomberg School of Public Health

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    Activities and Societies: Member of the Diversity and Inclusion Committee

    Ph.D. candidate in the Jordan lab.
    My thesis work focuses on the regulation of mammalian meiosis, with a focus on differences in protein function between males and females.

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    Activities and Societies: Alpha Lambda Delta First Year Honors Society, Ionic Society, Gamma Sigma Epsilon Chemistry Honor Society, Academic Judicial Council, Free Radicals Chemistry Club (President 2014-2015), Mortar Board Honors Society

    Majored in biochemistry while minoring in gerontology. Served as chair of the Academic Judicial Council. Participated in the 2013 Summer Research Institute through the Department of Chemistry & Physics. Received the Department of Chemistry and Physics Faculty Award in 2015.

Licenses & Certifications

Volunteer Experience

  • Alzheimer's Association® Graphic

    Volunteer

    Alzheimer's Association®

    - 5 months

    Health

    Assisted in day-to-day operations of the Western Maryland office. Helped organize events that resulted in over $100,000 fundraised.

  • Hospital Volunteer

    Frederick Regional Health System

    - 5 months

    Health

    Worked as a desk attendant in the Intensive Care Unit.

  • Woman to Woman Mentoring Graphic

    Mentor

    Woman to Woman Mentoring

    - Present 1 year 3 months

    Science and Technology

    Serving as a mentor for undergraduate students interested in pursuing science as a career.

Publications

  • PLK1 is required for chromosome compaction and microtubule organization in mouse oocytes

    Molecular Biology of the Cell

    Errors during meiotic resumption in oocytes can result in chromosome missegregation and infertility. Several cell cycle kinases have been linked with roles in coordinating events during meiotic resumption, including polo-like kinases (PLK). Mammals express four kinase-proficient PLKs, (PLK1-4). Previous studies assessing the role of PLK1 have relied on RNA knockdown and kinase inhibition approaches, as Plk1 null mutations are embryonically lethal. To further assess the roles of PLK1 during…

    Errors during meiotic resumption in oocytes can result in chromosome missegregation and infertility. Several cell cycle kinases have been linked with roles in coordinating events during meiotic resumption, including polo-like kinases (PLK). Mammals express four kinase-proficient PLKs, (PLK1-4). Previous studies assessing the role of PLK1 have relied on RNA knockdown and kinase inhibition approaches, as Plk1 null mutations are embryonically lethal. To further assess the roles of PLK1 during meiotic resumption, we developed a Plk1 conditional knockout (cKO) mouse to specifically mutate Plk1 in oocytes. Despite normal oocyte numbers and follicle maturation, Plk1 cKO mice were infertile. From analysis of meiotic resumption, Plk1 cKO oocytes underwent nuclear envelope breakdown with the same timing as control oocytes. However, Plk1 cKO oocytes failed to form compact bivalent chromosomes, and localization of cohesin and condensin were defective. Furthermore, Plk1 cKO oocytes either failed to organize α-tubulin or developed an abnormally small bipolar spindle. These abnormalities were attributed to aberrant release of microtubule organizing center (MTOC) linker protein, C-NAP1, and the failure to recruit MTOC components and liquid-like spindle domain factors (LISD). Ultimately, these defects result in meiosis I arrest prior to homologous chromosome segregation.

    Other authors
    See publication
  • Photochemical dynamics of a trimethyl-phosphine derivatized [FeFe]-hydrogenase model compound

    Chemical Physics

    Though there have been many studies on photosensitizers coupled to model complexes of the [FeFe]-hydrogenases, few have looked at how the models react upon exposure to light. To extract photoreaction information, ultrafast time-resolved UV/visible pump, IR probe spectroscopy was performed on Fe2(μ-S2C2H4)(CO)4(PMe3)2 (2b) dissolved in heptane and acetonitrile and the photochemical dynamics were determined. Excitation with 532 and 355 nm light produces bleaches and new absorptions that decay to…

    Though there have been many studies on photosensitizers coupled to model complexes of the [FeFe]-hydrogenases, few have looked at how the models react upon exposure to light. To extract photoreaction information, ultrafast time-resolved UV/visible pump, IR probe spectroscopy was performed on Fe2(μ-S2C2H4)(CO)4(PMe3)2 (2b) dissolved in heptane and acetonitrile and the photochemical dynamics were determined. Excitation with 532 and 355 nm light produces bleaches and new absorptions that decay to half their original intensity with time constants of 300 ± 120 ps and 380 ± 210 ps in heptane and acetonitrile, respectively. These features persist to the microsecond timescale. The dynamics of 2b are assigned to formation of an initial set of photoproducts, which were a mixture of excited-state tricarbonyl isomers. These isomers decay into another set of long-lived photoproducts in which approximately half the excited-state tricarbonyl isomers recombine with CO to form another complex mixture of tricarbonyl and tetracarbonyl isomers.

    Other authors
    See publication
  • Bioinformatic Characterization of Mosquito Viromes within the Eastern United States and Puerto Rico: Discovery of Novel Viruses

    Evolutionary Bioinformatics

    Abstract:
    Mosquitoes are efficient, militarily relevant vectors of infectious disease pathogens, including many RNA viruses. The vast majority of all viruses are thought to be undiscovered. Accordingly, recent studies have shown that viruses discovered in insects are very divergent from known pathogens and that many of them lack appropriate reference sequences in the public databases. Given that the majority of viruses are likely still undiscovered, environmental sampling stands to provide…

    Abstract:
    Mosquitoes are efficient, militarily relevant vectors of infectious disease pathogens, including many RNA viruses. The vast majority of all viruses are thought to be undiscovered. Accordingly, recent studies have shown that viruses discovered in insects are very divergent from known pathogens and that many of them lack appropriate reference sequences in the public databases. Given that the majority of viruses are likely still undiscovered, environmental sampling stands to provide much needed reference samples as well as genetic sequences for comparison. In this study, we sought to determine whether samples of mosquitoes collected from different sites (the Caribbean and locations on the US East Coast) could be differentiated using metagenomic analysis of the RNA viral fraction. We report here distinct virome profiles, even from samples collected short distances apart. In addition to profiling the previously known viruses from these samples, we detected a number of viruses that have been previously undiscovered.

    Other authors
    • Kenneth G. Frey
    • Theron Hamilton
    • Carlos J. Santos
    • Guillermo Pimentel
    • Vishwesh P. Mokashi
    • Kimberly A. Bishop-Lilly
    See publication

Courses

  • Biochemical and Biophysical Principles

    ME 100.710

  • Biological Chemistry I

    CHEM 301

  • Biological Chemistry II

    CHEM 402

  • Biological Chemistry Lab Techniques

    CHEM 403

  • Cell Biology

    BIOL 339

  • Cell Structure and Dynamics

    ME.110.728

  • Chemical Literature

    CHEM 270

  • Fundamentals of Genetics

    ME.260.708

  • Genetics

    BIOL 316

  • Genome Integrity and Cancer

    PH.120.624

  • Human Health Mosaic

    BIOL 138

  • Introduction to Cell Biology and Genetics

    BIOL 203

  • Introductory Physics I

    PHYS 203

  • Introductory Physics II

    PHYS 204

  • Macromolecular Structure and Analysis

    ME 100.709

  • Microbiology

    BIOL 331

  • Organic Chemistry I

    CHEM 209

  • Organic Chemistry II

    CHEM 210

  • Pathways and Regulation

    ME.360.728

  • Quantitative Analysis

    CHEM 215

  • Quantum Mechanics

    CHEM 431

  • Quantum Mechanics Lab

    CHEM 433

  • Responsible Conduct of Research

    PH.550.600

Languages

  • Spanish

    Limited working proficiency

Organizations

  • Bio Buzz

    Ambassador of Buzz

    - Present

    Helping to build and connect the network of life-science professionals in the Mid-Atlantic and beyond.

  • Women in Bio

    Member

    - Present
  • Doctoral Student Council

    Department Representative and Benefits Subcommittee Member

    - Present

    The committee consists of 1-2 Ph.D. students from each department across the school. We work with administrators to ensure that student needs are being met. I serve on the benefits subcommittee, which aims to make students more aware of the wellness benefits available to them.

  • Diversity and Inclusion Committee, Biochemistry and Molecular Biology Department

    Member

    - Present

    Our group organizes events to encourage an inclusive atmosphere in the department. As a member, I've helped to lead our "Diversity & Donuts" events (a monthly casual discussion session focused on a different diversity topic). I've also organized our monthly newsletters.

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