Life and education
Hooker grew up just outside of Asheville,Research and achievements
Hooker relocated to Charlestown, MA in 2009 at the initiation of his independent research career at the Martinos Center. He co-designed and scratch-built a cyclotron and radiopharmacy facility housing a Siemens Eclipse HP Cyclotron, completed early 2011. The production and imaging facility – part of the Martinos Center Research Core – provides imaging tools for all stages of translational research. The mission of his academic research lab is "to accelerate the study of the living, human brain and nervous system through development and application of molecular imaging agents." An organic chemist by training, Hooker and his research group are devoted to enhance understanding of the healthy brain and dysfunction in diseases including Alzheimer's, Autism and Schizophrenia. His research focus centers on the themes of neuroepigenetics, radiochemistry methods development and neuroimaging methods development; highlights are provided in the following section.Major publication themes
Hooker has published over 100 papers most notably in the domains of:Neuroepigenetics: visualizing histone deacetylase enzymes with PET
Work from Hooker's group published in August 2016'' –'' Wey & Gilbert ''et al'' 2016 ''Science Translational Medicine'' revealed the first visual maps of neuroepigenetic function in the living human brain using the Class-I histone deacetylase (HDAC) PET imaging probe 11C">sup>11Cartinostat. This work demonstrated a link between quantitative HDAC maps of the brain and the expression of plasticity and disease-related genes under HDAC control. The human imaging report was built on a background of tool development in the Hooker lab spanning seven years, wherein small molecule histone deacetylase (HDAC) inhibitors were systematically screened and refined to resolve chemical leads with Class-I HDAC isoform selectivity, outstanding brain penetrance and appropriate binding kinetics. The first-in-human imaging paper set the stage for Hooker's ongoing work to measure and map HDAC density, distribution and connectivity in diverse diseases, ''in vivo.''Radiochemistry methods development: changing the chemical landscape for PET tracer production
Hooker and his colleagues have made remarkable advances innovating in chemical and radiochemical synthetic methods to increase efficiency and expand capabilities of PET imaging. The most common radioisotopes for medical imaging agents, carbon-11 and fluorine-18, have a half-lives of 20.4 and 109.8 minutes, respectively. This presents significant demands in streamlining chemical synthesis steps and maximizing reaction yields in order to resolve sufficient quantities of radiotracer to complete required quality control steps before a dose can be 'released' for injection into a human subject. A critical element to this innovation has been the collaborative research environment cultivated within Hooker's lab to rethink dogmatic approaches to chemical endpoints or adapt cutting-edge organometallic chemistry to meet the needs of radiotracer synthesis. ''Research Highlights in Radiochemistry'' * In a 2011 ''Science'' paper, in collaboration with Tobias Ritter's lab at Harvard, Hooker demonstrated for the first time that a palladium-IV complex could fundamentally 'switch' the way fluoride behaves in chemical reactions, most aptly described as a switch from a nucleophile to an electrophile. In a separate and subsequent advance, this unconventional mindset led to the first demonstration of a concerted nucleophilic aromatic substitution reaction, published in ''Nature'' in 2016. * Hooker and Stephen Buchwald (MIT) developed a strategy for labeling molecules with carbon-11 using cyanide nearly instantaneously using a biaryl phosphine Pd(0) complexes. * Hooker and John T. Groves (Princeton) demonstrated the first example ofNeuroimaging methods development: ''functional'' MR and PET brain imaging
''A new application for radiolabeled glucose:'' The main energy source of the brain, glucose, provides a significant biological foothold to image brain activity via energy use through cellular uptake and trapping of the glucose analog, 18F">sup>18Fludexyglucose ( FDG). Since the mid-1970s, FDG has been applied as a 'bolus' at the beginning of an imaging experiment with regional uptake measured and mapped after a waiting period during which brain cells unknowingly substitute radiolabeled FDG for normal glucose. Like long-exposure photographs, bolus FDG PET imaging paradigms are robust and valuable in identifying otherwise-inaccessible tissue types with differential metabolism (e.g. cancerous tumors, post-ischemic myocardial lesions, hypometabolic brain regions following aneurysm), but lack kinetic detail. Despite some 40 years of 18F">sup>18FDG access and research, the ''dynamics'' of glucose utilization in response to brain activation remain poorly understood. Through innovations in radiotracer delivery and PET image processing, Prof. Hooker and his team were able to develop a method for brain glucose monitoring that produced something more like a movie, reporting changes in glucose use in response to multiple stimuli during a single PET scan. The lab is now expanding the concept of dynamic, functional PET imaging to measure real-time neurotransmitter release in the living human brain. ''Evidence of glial activation in the brain with chronic low back pain:'' In a similar reconfiguration of existing tools, Hooker and his faculty colleague and fMRI expert, Marco Loggia were the first to use the novel technology of integrated positron emission tomography-magnetic resonance imaging with the radioligand 11C">sup>11CPBR28 to demonstrate increased brain levels of the translocator protein (TSPO), a marker of glial activation, in patients with chronic low back pain. The work not only provided a new biological mechanism to explore in chronic pain treatment, it also helped to spark a major programmatic theme at MGH in neuroinflammation; borne from this was the Boston-wide Neuroinflammation Think Tank which bridges together major stakeholders from academia, medicine, and the pharmaceutical industry.Awards and honors
In 2016, Hooker was named as a Phyllis and Jerome Lyle RappaporReferences