M. Sc. Diana Mollocana Yanez

  • Scientific Assistant

Department of Nutritional Nutritional Science (140a)

Garbenstraße 30 Room 154
70599 Stuttgart

+49 (0)711 459 23590

 

M. Sc. Diana Mollocana Yanez 

 

 
 

Curriculum Vitae

Oct 2021 – Nov 2024: M.Sc. in Chemical Biotechnology, Technical University of Munich (TUM) – TUM Campus Straubing for Biotechnology and Sustainability & TUM Campus Garching

Internship and Master’s thesis: Strategies for the biochemical characterization and enzyme engineering of terpene synthases – Werner Siemens Chair of Synthetic Biotechnology

Jan 2018 – Aug 2021: Laboratory Technician and Research & Teaching Assistant, Plant Biotechnology Laboratory, Universidad San Francisco de Quito (USFQ), Quito, Ecuador

Aug 2012 – Dec 2017: B.Sc. in Biotechnological Process Engineering, Universidad San Francisco de Quito (USFQ), Ecuador

Five-year Engineering Degree Program

Junior Researcher in the Computational and Theoretical Chemistry Group (QCT), working on dengue virus proteases

Junior Researcher at the Biomedical Research Institute of Universidad de las Américas (UDLA) and at the Institute of Microbiology, USFQ, Department of Parasitology and Vectors

Bachelor’s thesis: Pilot study on the transmission dynamics of Ascaris spp. between humans and pigs in rural and semi-urban populations.

Research interests:

Diana Mollocana Yanez’s research focuses on the functional characterization of lipocalins, a group of transport proteins, using computer-aided and experimental in vitro and in vivo methods. To investigate protein-ligand interactions, she is establishing protocols for microscale thermophoresis (MST). Another focus of her work is metabolic studies in mouse models, which are complemented by molecular analyses to determine protein function. Currently, she is particularly interested in mouse major urinary proteins (MUPs) and their role in lipid transport and metabolism. In the long term, her research aims to contribute to a better understanding of metabolic diseases such as fatty liver disease, diabetes, and obesity, which are influenced by the interplay of diet, sex, and genotype. 

Publications

M.Sc. Diana Mollocana Yanez

Mollocana, D. (2024). Figure.1. Primary and quaternary structures of the SARS-CoV-2 spike protein. Verwendet in Kapitel 3 (Structural and functional properties of the SARS-CoV-2 spike protein: Potential vaccine and drug development for COVID-19, by Berkowitz, R.& Ostrov, D.), Seite 58. Understandig the Pandemic. Pathophysiology, Transmission, and Treatment of COVID-19. Von Marco Cascella. ISBN: 9780443290046, 0443290040. https://doi.org/10.1016/B978-0-443-19170-1.00013-9

Leon, B., Montero-Oleas, A., Mollocana, D., Calderon, D., Torres, M.L. (2022). Optical aptasensor for in situ detection and quantification of methylxanthines in Ilex guayusa. ACI: Avances en Ciencias e Ingenieria. 14 (1):2301. https://doi.org/10.18272/aci.v14i1.2301

Mollocana, D. (2021). Figure 17.3: SARS-CoV2 Spike Glycoprotein Structure. Verwendet in Kapitel 17 (Directed Therapies to Nucleic Acids and Cytoplasmic RNA, by Ghose, M.), Seite 455. Organelle and Molecular Targeting. Von Lara Scheherezade Milane und Mansoor M. Amiji. CRC. ISBN: 9780367551377. https://doi.org/10.1201/9781003092773-19

Mollocana, D., Erazo, M.P., Aguirre, X. Torres, M.L. (2019). Molecular characterization of Moniliophthora roreri, causative agent of moniliasis in cocoa in three provinces of Ecuador: Los Rios, Manabi and Santo Domingo de los Tsáchilas. MOL2NET 2019, International Conference on Multidisciplinary Sciences, 5th edition. https://doi.org/10.3390/mol2net-05-06382

Burgos, G., Yanqui-Rivera, F., Mollocana, D., Camargo, M., Zapata, S. (2017). Multiplex PCR in non-human DNA molecular identification of Ascaris spp. In forensic biology. Forensic Science International: Genetics Supplement Series 6, e568-e569. https://doi.org/10.1016/j.fsigss.2017.09.227

Aguilera-Pesantes, D., Robayo, L.E., Méndez, P.E., Mollocana, D., Marrero-Ponce, Y., Torres, F.J., Méndez, M.A. (2017). Discovering key residues of dengue virus NS2b-NS3-protease: New binding sites for antiviral inhibitors design. Biochemical and Biophysical Research Communications 492(4):631-642.https://doi.org/10.1016/j.bbrc.2017.03.107