Research Associate or Postdoctoral Fellow at Tufts University, Graduate Sciences and Medical School Campus, Boston
Overview: A high proportion of the elderly suffer from age-related loss of vision. We elucidate relationships between environmental stress, physiologic stress responses, protein quality control and eye function in order to discover mechanisms of aging, and nutritional and other means to delay age-related vision impairments such as age-related macular degeneration and cataracts. Projects are mature and much data is already available. Tufts Medical Center is a highly collaborative and productive environment in downtown Boston, within ~20 minutes from Harvard, MIT, Boston Univ. The lab is funded by NIH, USDA, several foundations.
Position Description: We seek outstanding candidates with a recent PhD in Biochemistry or a related discipline to work on one of the following funded projects:
1) Discovering novel stress-induced ubiquitin and autophagy enzyme interactions in response to glycative stress.
2) Regulatory mechanisms of eye lens differentiation,
3) Elucidate interactions between dietary glycemia, metabolomics, microbiome, AMD, cataract, and aging in animal studies and/or human populations, including planning randomized intervention studies.
The following are important: training in biochemistry or a related discipline, bioinformatics, histology, analyzing large data sets, animal husbandry. Candidates should have at least two English language first authored papers and 1 year of experience. A 2 year commitment is required. Preference will be given to candidates who have permits to reside in the USA. All candidates must have or obtain a suitable visa.
Selected recent papers from our group include
Rowan, S., et al., (2020) A low glycemic diet protects disease-prone Nrf2-deficient mice against age-related macular degeneration, Free Radical Biology and Medicine PMID: 32068111 DOI: 10.1016/j.freeradbiomed.2020.02.010
Aragonès, G. et al., Autophagic receptor p62 protects against glycation-derived toxicity and enhances viability, Aging Cell, PMID: 33146912 DOI: 10.1111/acel.13257
Whitcomb, E. A. et al. Stabilization of p27(Kip1)/CDKN1B by UBCH7/UBE2L3 catalyzed ubiquitinylation: a new paradigm in cell-cycle control. FASEB J. (2019). PMID: 30113882.
Rowan, S. et al. Involvement of a gut–retina axis in protection against dietary glycemia-induced age-related macular degeneration. Proc. Natl. Acad. Sci. (2017). PMID: 28507131.
Lyu, L. et al. Unfolded-protein response-associated stabilization of p27(Cdkn1b) interferes with lens fiber cell denucleation, leading to cataract. FASEB J. (2016). PMID: 26590164.
Liu, K. et al. Altered ubiquitin causes perturbed calcium homeostasis, hyperactivation of calpain, dysregulated differentiation, and cataract. Proc. Natl. Acad. Sci. (2015). PMID: 25583491.
Chaffee, B. R. et al. Nuclear removal during terminal lens fiber cell differentiation requires CDK1 activity: appropriating mitosis-related nuclear disassembly. Development (2014). PMID: 25139855.
Our Center is currently officially open with restricted access. Training can begin in January 2021. We will start part time and move to full time when we are permitted to work in the building.
Application Instructions: Please send a CV, names of three references (including PhD advisor and post doc mentor) and a list of grades received in Graduate science courses to:
Allen Taylor, Director of the Nutrition and Vision Research Laboratory at the HNRCA
Professor of Nutrition, Chemical and Molecular Biology, and Ophthalmology at Tufts University
JM-USDA HNRCA, 711 Washington St, Boston, MA 02111
For questions about these positions, please contact Dr. Taylor at 617 784 3199 3-5 PM Eastern Time.
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