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Volume 7, Issue 1 (Suppl)

J Biotechnol Biomater

ISSN: 2155-952X JBTBM, an open access journal

March 20-21, 2017 Rome, Italy

&

15

th

World Congress on

2

nd

International Conference on

Biotechnology And Biotech Industries Meet

Enzymology and Molecular Biology

Enzymology & Mol. Biology 2017

Biotechnology Congress 2017

March 20-21, 2017

The catalytic and structural roles of the Human Hexokinase 2 in cancer

Wael M Rabeh

New York University Abu Dhabi, UAE

G

lucose metabolism is 200 times higher in cancer affected tissues in comparison to normal tissue as a strategy to support tumor

growth and progression, historically known as the ‘Warburg effect’. Hexokinase is the first enzyme of the glycolytic pathway

that catalyzes the phosphorylation of glucose for its activation to glucose-6-phosphate and uses ATP as high-energy source of

phosphates. Four isozymes are present in human body with hexokinase 2 (HK2) as most active and specifically expressed in variety

of different cancers. However, HK2 binding to the outer mitochondrial membrane not only gives it prime access to ATP generated

by the mitochondrial but inhibit apoptosis. Here, we aim to biochemically and structurally characterize interactions of HK2 with

the mitochondria and the N-terminal role in catalysis and stability of the full-length enzyme. Here, we solved the crystal structure

of human HK2 in complex with glucose and glucose-6-phosphate (PDB code: 2NZT), where it is a homodimer with catalytically

active N- and C-terminal domains linked by a seven-turn α-helix. Different from the inactive N-terminal domains of isozymes 1

and 3, the N-domain of HK2 is not only capable of catalyzing reaction but it is also responsible for thermodynamic stabilization of

the full-length enzyme. Deletion of first α-helix of the N-domain that binds to the mitochondria altered the stability and catalytic

activity of the full-length HK2. In addition, we found the linker helix between the N- and C-terminal domains to play an important

role in controlling the catalytic activity of the N-terminal domain. HK2 is a major step in the regulation of glucose metabolism in

cancer making it an ideal target for the development of new anticancer therapeutics. Characterizing the structural and molecular

mechanisms of human HK2 and its role in cancer metabolism will accelerate the design and development of new cancer therapeutics

that are safe and cancer specific.

Biography 

Wael M Rabeh has received his PhD in Biochemistry from the Lab of Professor Paul F Cook, where he characterized the last enzymatic reaction of the cysteine

biosynthetic pathway in

Salmonella typhimurium

. In 2005, he joined the Structural Genomic Consortium (SGC) at the University of Toronto as a Post-doctoral

Fellow, where he characterized the 3D structure of human proteins with medical relevance using X-ray crystallography. In 2007, he joined the Lab of Dr. Gergely

Lukacs at McGill University for the characterization of a membrane channel that is the main cause of cystic fibrosis. His research focuses on the characterization

of protein structures and mechanism to understand their biological functions.

wael.rabeh@nyu.edu

Wael M Rabeh, J Biotechnol Biomater 2017, 7:1(Suppl)

http://dx.doi.org/10.4172/2155-952X.C1.070