Howard Ronald Kaback
H. Ronald Kaback | |
---|---|
Born |
Philadelphia, United States of America | June 5, 1936
Other names | Ron Kaback |
Occupation | Molecular Biologist, Biochemist |
Years active | 1960 - present |
Spouse(s) | Molly Kaback |
Awards |
Rosenstiel Award (1974) Member of the American Academy of Arts and Sciences (1986) Member of the National Academy of Sciences (1987) Anatrace Membrane Protein Award (2007) Distinguished Alumni Achievement Award (2009) Peter Mitchell Memorial Medal (2012) |
Website | http://149.142.237.181/H.R._Kaback.html |
Howard Ronald Kaback is an American Biochemist, known for Kabackosomes, the cell-free membrane transport vesicles. He is the brother of Michael M. Kaback, pediatrician and human geneticist, who developed a screening program to detect and prevent Tay-Sachs disease, a rare and fatal genetic disorder most common in Ashkenazi Jews.[1]
Biography
Prof. H. Ronald Kaback was born in Philadelphia, PA. He earned his BS at Haverford Collage in 1958 and his MD at The Einstein College of Medicine in 1962.[2] He interned at the Bronx Municipal Hospital Center in Pediatrics and did pre- and postdoctoral research at Einstein College in the laboratory of Adele B. Kostellow. In 1964 he moved to National Heart Institute to the laboratory of Earl R. Stadtman.
In 1970, he joined the Roche Institute of Molecular biology in Nutley, NJ where he later became Head of Biochemistry. In 1989 he became an Investigator of the Howard Hughes Medical Institute and Professor of Physiology and Microbiology, Immunology & Molecular Genetics, as well as a member of the Molecular Biology Institute at the University of California Los Angeles.[3]
Career
Ronald Kaback became interested in membrane transport at a time when studies on biological membranes were in their infancy, and in the early phase of his career, he developed a cell-free membrane system to study active transport. The system consisted of osmotically sealed membrane vesicles of defined orientation (right-side-out) that catalyze active transport essentially as well as intact cells, but lack subsequent metabolism of the solutes accumulated. These vesicles were dubbed Kabackosomes by the Dutch scientist Wilhelmus N. Konings, Kaback’s close friend and early collaborator. In addition to transforming the field of transport from phenomenology to biochemistry, this seminal development caused him to forego the practice of pediatrics for a career in basic science. The use of membrane vesicles from various sources has become a standard tool for testing models and performing hypothesis-driven research.
Kaback demonstrated quantitatively that an electrochemical H+ gradient is the immediate driving force for accumulation of many different solutes. Peter Mitchell who conceived and formulated the ‘’Chemiosmotic Hypothesis’’ considered these findings to be the most conclusive experimental support for the Hypothesis with respect to membrane transport. Kaback extended his interest to the molecular mechanism of membrane transport by focusing on the lactose permease of Escherichia coli (LacY; aka the lactose/H+ symporter), which is now a paradigm for the Major Facilitator Family, arguably the largest group of membrane transport proteins.[4][5] With the emergence of molecular biology, he and his colleagues pioneered ' Cysteine-Scanning Mutagenesis in combination with chemical modification, as well as a battery of site-directed biophysical/biochemical techniques to demonstrate almost incontrovertibly that LacY functions by a mechanism involving alternating access of sugar- and proton-binding sites to either side of the membrane.[6] This general experimental approach is recognized today and has become a standard tool for membrane protein research. Without a crystal structure, Kaback and colleagues succeeded in using the approach to obtain essential information about helix packing, the organization of the sugar-binding site and the residues involved in H+ translocation and coupling.
He and his colleagues then obtained an X-ray crystal structure of LacY, an essential step towards understanding the molecular mechanism, which has had important impact on the field of membrane transport.[7] Ronald Kaback gives lectures regularly at international meetings.[8] His laboratory continues to extend studies on the mechanism of LacY and other symport proteins.
Awards and recognitions
- Lewis S. Rosenstiel Award (1973)[9]
- Member of the American Academy of Arts and Sciences (1986)[10]
- Member of the National Academy of Sciences (1987)[11]National Academy of Sciences (1987)[12]
- Anatrace Membrane Protein Award (2007)[13]
- Distinguished Alumni Achievement Award (2009)
- Peter Mitchell Memorial Medal (2012)
Selected publications
The results of Kaback’s studies are described in over 450 publications[13] in peer-reviewed scientific journals. His research is also chronicled in textbooks, reference books and teaching materials in many languages for both undergraduate and graduate teaching.
- Kaback, H. R. (1968). "The role of the phosphoenolpyruvate-phosphotransferase system in the transport of sugars by isolated membrane preparations of Escherichia coli". J. Biol. Chem 243 (13): 3711–24. PMID 4872728.
- Kaback, H. R. (1971). "Bacterial membranes". Methods Enzymol 22: 99–120. doi:10.1016/0076-6879(71)22015-2.
- Ramos, S.; Schuldiner, S.; Kaback, H. R. (1976). "The electrochemical gradient of protons and its relationship to active transport in Escherichia coli membrane vesicles". Proc. Natl. Acad. Sci. USA 73 (6): 1892–1896. doi:10.1073/pnas.73.6.1892. PMID 6961.
- Newman, M. J.; Foster, D.; Wilson, T. H.; Kaback, H. R. (1981). "Purification and reconstitution of functional lactose carrier from Escherichia coli". J. Biol. Chem 256 (22): 11804–11808. PMID 7028742.
- Foster, D. L.; Boublik, M.; Kaback, H. R. (1983). "Structure of the lac carrier protein of Escherichia coli". J. Biol. Chem 258 (1): 31–34. PMID 6336750.
- "Cys-scanning mutagenesis: a novel approach to structure function relationships in polytopic membrane proteins" 12 (13). October 1998: 1281–99. PMID 9761772.
- Abramson, J.; Smirnova, I.; Kasho, V.; Verner, G.; Kaback, H.R.; Iwata, S. (2003). "Structure and Mechanism of the Lactose Permease of Escerichia coli". Science 301 (5633): 610–615. doi:10.1126/science.1088196. PMID 12893935.
- Kaback, H.R.; Dunten, R.; Frillingos, S.; Venkatesan, P.; Kwaw, I.; Zhang, W.; Ermolova, N. (2007). "Site-directed alkylation and the alternating access model for LacY". Proc Natl Acad Sci USA 104 (2): 491–494. doi:10.1073/pnas.0609968104. PMID 17172438.
- Guan, L.; Mirza, O.; Verner, G.; Iwata, S.; Kaback, H.R. (2007). "Structural determination of wild-type lactose permease". Proc Natl Acad Sci USA 104 (39): 15294–15298. doi:10.1073/pnas.0707688104. PMID 17881559.
- Smirnova, I.; Kasho, V.; Choe, J.-Y.; Altenbach, C.; Hubbell, W. L.; Kaback, H.R. (2007). "Sugar binding induces an outward facing conformation of LacY". Proc Natl Acad Sci USA 104 (42): 16504–16509. doi:10.1073/pnas.0708258104. PMID 17925435.
- Smirnova, I.; Kasho, V.; Sugihara, J.; Kaback, HR. (2011). "Opening the periplasmic cavity in lactose permease is the limiting step for sugar binding". PNAS 108 (37): 15147–15151. doi:10.1073/pnas.1112157108. PMID 21896727.
External links
- Howard Kaback University of California, Los Angeles
- Kaback Lab and H. R. Kaback University of California, Los Angeles
- Ronald Kaback, M.D. at David Geffen School of Medicine University of California, Los Angeles
- Scientist studies 'third amino acid from left' University of California, Los Angeles
- Lecture on YouTube
- Profile
References
- ↑ Kaback, Michael (2001). Tay-Sachs Disease. Academic Press. ISBN 0120176440.
- ↑ "Ronald Kaback M.D. | David Geffen School of Medicine at UCLA". People.healthsciences.ucla.edu. Retrieved 2014-05-14.
- ↑ Kaback, Howard Ronald (1989). "Professor- UCLA".
- ↑ Kaback, Howard Ronald; Smirnova I; Kasho V. (2011). "Lactose Permease and the Alternating Access Mechanism". Biochemistry 50 (45): 9684–9693. doi:10.1021/bi2014294. PMC 3210931. PMID 21995338.
- ↑ Madej, M. Gregor; Kaback, H. Ronald (2014). "The Life and Times of Lac Permease: Crystals Ain’t Everything, but They Certainly Do Help". In Krämer, R. & Ziegler, Ch. Membrane Transport Mechanism 3D Structure and Beyond. Heidelberg, New York, Dordrecht, London: Springer. pp. 121–158. ISBN 978-3-642-53838-4.
- ↑ Kaback, Howard Ronald; Frillingos S; Sahin-Toth M; Wu J. (1998). "Cys-scanning mutagenesis: a novel approach to structure function relationships in polytopic membrane proteins". FASEB J. 12 (13): 1281–99. PMID 9761772.
- ↑ Kaback, Howard Ronald; Abramson J; Smimova I; Kasho V; Verner G; Iwata S. (2003). "Structure and mechanism of the lactose permease of Escherichia coli". Science 301 (5633): 610–5. Bibcode:2003Sci...301..610A. doi:10.1126/science.1088196. PMID 12893935.
- ↑ Hopkin, Karen (May 1, 2011). "Making the Gradient". The Scientist 25 (5).
- ↑ "Rosenstiel Award Past Winners". Rose.brandeis.edu. Retrieved 2014-05-14.
- ↑ https://www.amacad.org/multimedia/pdfs/alphalist.pdf
- ↑ List of Members 1780–present (PDF, 207 kB) bei der American Academy of Arts and Sciences (amacad.org); abgerufen am 29. Mai 2012
- ↑ "H. Ronald Kaback". Nasonline.org. 1993-09-19. Retrieved 2014-05-14.
- 1 2 "UCLA Molecular, Cellular and Integrative Physiology Interdisciplinary Program". Mcip.ucla.edu. Retrieved 2014-05-14.
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