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Author Archive for: "winzeler"

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Sindhu Daggupati

I am an undergraduate student who is interested in learning more about how drug resistance medication works within the human body and I am also interested in becoming a pediatric surgeon one day.

Lisa Pham

I’m an undergraduate student studying chemical engineering and interested in drug resistance research.

Alani Diamond

Richard Tram

I am a Global Health undergraduate student nurturing mosquitoes used for studying malaria cultures.

Tuo Yang, Ph.D.

Adryanna Nguyen

I am an undergraduate student that is interested in how organisms evolve to become resistant to certain drugs over time.

Karla Godinez

I received my M.S. degree in Bioinformatics in May 2019 where I constructed a pipeline to get insight into the differential gene expression using Illumina RNA-seq data. As part of the MalDA team, I use Bio/Cheminformatics tools and modeling algorithms to support the work in drug targets and resistance mechanisms identification aiming to discover novel therapeutics for the treatment of Plasmodium falciparum.

Krypton Carolino

Plasmodium parasites are becoming resistant to the currently available drug treatments for malaria, thus there is a necessity to develop new medicines. I am interested in studying irresistibles, compounds that can kill parasites without being toxic to the host or conferring resistance within the parasites. I plan to utilize biochemical assays to unravel the mechanisms of action of these compounds.

Rachel Findlay

I am an undergraduate biology student working with Plasmodium cultures to identify potential drug targets.

Lauren Midyett

I am an undergraduate student majoring in Bioengineering. I contribute to the mosquito dissections as well as analyzing readout data from the liver and asexual blood stage assays to determine their success.

Natalia Koga

A third year undergraduate biochemistry and cell biology major. I am doing research with plasmodium infected blood cells, using antimalarial drug selections to find resistance among the cells in order to target underlying genetic mechanisms.

Ashley You

I am an undergraduate student studying General Biology and I work with yeast cultures to identify potential drug targets.

Ioana Vestemean

I am a fourth year undergraduate Biochemistry and Cell Biology major. I work with plasmodium infected red blood cells under drug pressures and am interested in finding signs of a drug resistance in these cells so more information can be uncovered about the gene targets of these antimalarial drugs.

Sabine Ottilie, Ph.D.

As the project manager of the MalDA Consortium, I am coordinating the efforts of multiple labs to discover the next generation of antimalarial drugs.

In addition, I am leading the efforts of Team Yeast to identify compounds with primary activity against eukaryotic pathogens causing diseases such as Malaria, Chagas’ disease, Schistosomiasis, Cryptosporidiosis and fungal infections and determine their cellular targets. Our approach utilizesa sensitized, attenuated strain of Saccharomyces cerevisiae, in vitro directed evolution and whole genome sequencing. By analyzing how yeast genetically adapts to treatment with small cytotoxic molecules we identify the compounds’ targets and/or targeted pathways, predict resistance mechanisms, and define sites of compound/protein interactions.

Miranda Song

I am an undergraduate bioengineering student working with Plasmodium cultures to identify potential drug targets.

Korina Eribez

Lab Manager
Area Safety Officer
SRA2
High-Throughput Screening
Drug Target Identification

Juan Carlos Jado, Ph.D.

I completed my PhD in June 2014 in renal pathophysiology in Madrid. As a postdoc, I have 2 main projects:

1) As part of the Malaria Drug Accelerator (MalDA) team, I work in the identification of drug targets, novel genes and the corresponding non-synonymous coding variants involved in drug resistance of Plasmodium falciparum.

2) Chemogenetic characterization of antineoplastic drugs using in vitro evolution followed by whole genome analysis (IVIEWGA) to define the “resistome” of cancer cells. To simplify the identification of alleles in cancer resistome, I use a near-haploid chronic myelogenous leukemia cell line as a model. The identification of resistant alleles (both copy number and single nucleotide variants) will be validated by CRISPR-Cas9

Jacklyn Sanchez-Alvarez

I am an undergraduate public health student working with Plasmodium cultures to identify the compounds’ targets and/or targeted pathways, leading our team to predict resistance mechanisms through selections.

Monica Le

I am an undergraduate researcher working on directed evolution of Plasmodium cultures through liver stage and asexual blood stage assays in order to identify potential drug targets. In doing so, I am able to analyze which compounds are actively treating parasites and identify the compounds’ targets and/or targeted pathways, leading our team to predict resistance mechanisms through selections.

Ayden Fonseca

Undergraduate researcher working on the ABS and liver-stage projects. When I’m not carving up mosquitos, I am carving up waves.

Nimisha Mittal, Ph.D.

I received my Ph.D. in India, where I worked on the epigenetic regulators of the parasite Leishmania. In the Winzeler lab, I am a part of the high throughput screening (HTS) team for anti-malarial compounds. I conduct in vitro experiments for the identification of hits having liver stage and asexual blood stage specificity.

Christie Lincoln

I am an undergraduate student studying Human Biology and Computer Science. I contribute to the liver stage and asexual blood stage assays in the Winzeler lab.

Frances Rocamora, Ph.D.

Megan Verma

I am a third year Biochemistry/Cell Biology major with a Business minor. I am working on the gametocyte project in the Winzeler lab, as well as the asexual blood culture.

Jan M Economy

I am a Research Coordinator with the Winzeler lab. I am a media and communications professional with a Bachelors of Science degree focused in Business Administration-Statistical Management & Organizational Behavior from San Diego State University.

Lindsey Skokan

Undergraduate researcher working on the gametocyte project.

Madeline R. Luth

A major component of the MalDA collaboration is the generation of resistant Plasmodium falciparum lines through in vitro directed evolution. I utilize various bioinformatics tools to analyze the whole genome sequence information of these parasites as well as other eukaryotic pathogens for the purpose of identifying drug targets and resistance mechanisms.

Irwin W. Sherman, Ph.D.

The principal focus of our laboratory was to characterize in molecular terms the membrane structure and function of the erythrocyte infected by malaria parasites. Of particular interest was the mechanisms whereby red cells infected with the human malaria Plasmodium falciparum become adhesive. Using monoclonal antibodies, synthetic peptides and in vitro binding assays we identified an adhesive region of the erythrocyte that results from the exposure of cryptic residues of band 3 protein. Since retirement Professor Sherman has been a Visiting Scientist at the Scripps Research Institute (La Jolla, CA 92037).

For more information about Dr. Sherman, please visit: Irwin Sherman Ph.D.

Pamela Orjuela-Sanchez, Ph.D.

Led a team of three people responsible for high-throughput screens (~30K/year) using a high content imaging platform in the search for new molecules against P. falciparum gametocytes. I have also developed competencies performing other cell-based drug screenings (liver and blood malaria parasite stage) using luciferase and sybr green systems. I am enthusiastic about fluorescence microscopy and high content imaging.

Lawrence Wang

RT-qPCR Technician, general research tech.

Jennifer Yang

Kristen Thorne

Mclean Taggard

Emma Paytas

Jenya Antonova, Ph.D.

Jaeson Calla, Ph.D.

Annie Cowell, M.D./MPH

I am an Infectious Diseases physician in my third year of fellowship at UC San Diego. I am interested in how next generation sequencing of pathogens from patient samples can answer biological and epidemiological questions. In the Winzeler lab, my projects include using selective whole genome amplification to enrich Plasmodium vivax DNA from patient samples for whole genome sequencing, and using proteomics to better understand malaria liver stage infection.

Purva Gupta, Ph.D.

I work on the drug discovery of malaria. Together with the MDTIP Consortium, we try to understand the resistome and the drug-able genome of the malaria parasite. Making the parasite resistant to different compounds helps us find the mutations responsible for resistance and genes that confer resistance. On this basis we hope to find novel gene targets for the drug-like compounds. We are also trying to validate the gene targets for small molecules through CRISPR

Greg LaMonte, Ph.D.

I have been working to determine the mechanism of action of several classes of antimalarial compounds, using a combination of Plasmodium and yeast genetics and molecular biology. More recently, I have been focusing on examining parasite liver stage development using a combination of transcriptional analysis and site-specific proteomics.

Dylan Hutson

Andrea Cheung

Colleen Boyle

Caroline Page

I am apart of the yeast team in the Winzeler lab and my main objective is to identify drug targets through the direct evolution of yeast cells.

Melanie Zou

I test the potency of natural product compounds against blood stage malaria, and look at liver stage parasite protein expression through proteomics.

Erika Sasaki

I work with the MDTIP Consortium to discover novel drug targets in Plasmodium falciparum by generating lines resistant to small molecules and then sequencing these lines to discover resistance causing mutations. We then use CRISPR to validate these gene targets and are using radio labeling to run metabolic assays. I am currently working on my Senior Honors Thesis using four small molecules from the seventh round of compounds from BMGF.

Jake Schenken

I am a part of the yeast models for malaria team in the Winzeler Lab, which is responsible for performing drug target identification for potential anti-malarial compounds via directed evolution in drug-sensitive yeast strains and phenotypic screening. In addition, I am responsible for target validation by gene editing in yeast using the CRISPR-Cas9 system with Homology Directed Repair followed by phenotypic screening.

Prianka Kumar

I am an undergraduate researcher working on directed evolution of yeast cultures to identify potential drug targets as well as using recombinant DNA expression to validate target identification.

Peter Chebi

My research focuses on learning more about the sexual phase of Plasmodium falciparum, referred to as the gametocyte stage. I take pride in doing all I can to reduce the transmission rates of malaria.

Matthew Abraham

As hits are generated from our high-throughput screening pipeline, the tractability of these small molecules is required before therapeutic consideration. To parse out attractive scaffolds, I conduct in-vitro and in-silico target identification experiments, for multiple stages in the Plasmodium life cycle. These efforts have led to the identification of several unique scaffolds with potent liver-stage specificity, and previously uncharacterized druggable targets in the asexual blood stage of infection.

Biniam Ambachew

I work as an undergraduate researcher under the guidance of Jenya Antonova, Ph.D. on the malaria asexual blood stage assay (ABS) and the liver stage assay.