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Robert K. Crane

American biochemist From Wikipedia, the free encyclopedia

Robert K. Crane

Robert Kellogg Crane (December 20, 1919 – October 31, 2010) was an American biochemist best known for his discovery of sodium–glucose cotransport.

Quick Facts Born, Died ...
Robert K. Crane
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Born(1919-12-20)December 20, 1919
DiedOctober 31, 2010(2010-10-31) (aged 90)
EducationWashington College, Harvard
Known forCotransport
RelativesStephen Crane, novelist (greatuncle)
AwardsAmerican Gastroenterological Association Distinguished Achievement Award (1969)
Dr. Harold Lamport Award, New York Academy of Sciences (1977)
Scientific career
FieldsBiochemistry
InstitutionsWashington University in St. Louis
Chicago Medical School
Rutgers Medical School of the University of Medicine and Dentistry of New Jersey
Doctoral advisorFritz Lipmann
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Early life

Crane was born on December 20, 1919, in Palmyra, New Jersey, to Wilbur Fiske Crane, Jr. architect and engineer, and Mary Elizabeth McHale Crane. He is the grandson of Stephen Crane's brother Wilbur.[1]

He received a B.S. from Washington College in 1942. After serving in the Navy during World War II, Crane studied in biochemistry with Eric Ball at Harvard from 1946 to 1949, then spent a year with Fritz Lipmann at Harvard Medical School, and received a Ph.D. in Medical Sciences in 1950.

Career

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Perspective

He joined Carl Cori's Department of Biological Chemistry at Washington University School of Medicine in St. Louis, where he began his long interest in glucose metabolism and worked until 1962. After that, he was professor and chairman of the department of Biochemistry at the Chicago Medical School until 1966 and then became professor and chairman of the department of Physiology and Biophysics at Rutgers Medical School (now known as Robert Wood Johnson Medical School) of the University of Medicine and Dentistry of New Jersey until 1986. He received a Sc.D. from Washington College in 1982.[2]

In the 1950s, Crane played a central role in establishing that glucose transport into the cell was the first step in glucose metabolism and its control. He demonstrated that neither the phosphorylation-dephosphorylation mechanism nor other covalent reactions accounted for glucose transport in the intestine.

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Model of cotransport coupling of glucose transport to an Na+ pump by an Na+ circuit. Redrawn from Crane et al.[2][3]

In August 1960, in Prague, Crane presented for the first time his discovery of the sodium-glucose cotransport as the mechanism for intestinal glucose absorption.[3] Cotransport was the first ever proposal of flux coupling in biology and was the most important event concerning carbohydrate absorption in the 20th century.[4][5]

Crane's discovery of cotransport led directly to the development of oral rehydration therapy.[6][7] This treatment counterbalances the loss of water and electrolytes caused by cholera via a glucose containing salt solution that accelerates water and electrolyte absorption. This is possible because cholera does not interfere with sodium-glucose cotransport.[8][9]

Oral rehydration therapy saves the lives of millions of cholera patients in underdeveloped countries since the 1980s.[10] In 1978, The Lancet wrote: "the discovery that sodium transport and glucose transport are coupled in the small intestine, so that glucose accelerates absorption of solute and water, was potentially the most important medical advance this century."[11]

Crane's discovery is also used in blockbuster drugs, such as the SSRI Prozac, which treat depression by inhibiting the Na/serotonin cotransporters in the brain. Furthermore, major pharmaceutical companies are developing inhibitors of the Na/glucose cotransporters to treat diabetes and obesity.[12]

Awards and honors

Selected publications

Further reading

See also

References

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