South San Francisco
California, United States of America
A postdoctoral position is available in the Department of Early Discovery Biochemistry to develop peptide-based inhibitors of targets of therapeutic interest and investigate their mechanism of action by biochemistry, structural and cell biology approaches. The group utilizes a multidisciplinary molecular approach for lead identification and target validation. Recent efforts focus on the use of phage display to develop peptide-based probes for modulating protein-protein interactions, the development of cell permeable peptides and characterization of their cellular trafficking routes, as well as new targets in cancer biology and ophthalmology.
Successful candidates will be highly motivated to work independently in a collaborative environment. Candidates must have a Ph.D. in biochemistry, cell biology or related discipline. Candidates should have experience in protein chemistry, cellular biochemistry and state of the art molecular biology techniques as demonstrated by a first-author paper published or accepted in a peer-reviewed journal. A strong quantitative background and demonstrated expertise in recombinant protein expression and purification, protein engineering, analytical and biophysical methods, bioconjugation reactions, and phage diversity methods is desirable. Experience with tissue culture, cell-based assays and transfections, gene knockdown, gene expression analysis and fluorescence microscopy is a plus. The candidate must have strong analytical, collaborative, communication and organizational skills.
A Nile, F de Sousa E Melo, S Mukund, R Piskol, S Hansen, L Zhou, Y Zhang, Y Fu, E Gogol, L Kömüves, Z Modrusan, S Angers, Y Franke, C Koth, W Fairbrother, W Wang, F de Sauvage, RN Hannoush. A selective peptide inhibitor of Frizzled 7 receptors disrupts intestinal stem cells. Nature Chemical Biology 2018 Apr 9. doi: 10.1038/s41589-018-0035-2. [Epub ahead of print]
A Nile, S Mukund, K Stanger W Wang and RN Hannoush. Unsaturated fatty acyl recognition by Frizzled receptors mediates dimerization upon Wnt binding. PNAS 2017, 114, 4147-4152.
X Gao, K Stanger, H Kaluarachchi H, T Maurer, P Ciepla, C Chalouni, Y Franke, RN Hannoush. Cellular uptake of a cystine-knot peptide and modulation of its intracellular trafficking. Sci Rep. 2016, 6:35179.
K Stanger, T Maurer , H Kaluarachchi, M Coons, Y Franke, RN Hannoush. Backbone cyclization of a recombinant cystine-knot peptide by engineered Sortase A. FEBS Lett. 2014, 588, 4487-96.
X. Gao, RN Hannoush, Single-cell imaging of Wnt palmitoylation by the acyltransferase porcupine. Nature Chemical Biology 2014, 10, 61-68.
RN Hannoush, JL Sun, The chemical toolbox for monitoring protein fatty acylation and prenylation. Nature Chemical Biology 2010, 6, 498 - 506.
A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.
The next step is yours. To apply today, click on the "Apply online" button.
Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page.
At Genentech, we share salary ranges with applicants during the recruiting process, if requested. Third party salary estimates may not be accurate or up-to-date.
These are our stories - stories of the obstacles and opportunities that define and celebrate the unique people at Genentech