Press Release 96-066
Fertilization Protein Structure to Aid in Leukemia Treatment
October 30, 1996
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The structure of a protein recently discovered by C. D. Stout at the Scripps Research Institute in La Jolla, California, is providing insights into the details of the interaction between sperm and egg. Remarkably, the same structure may hold a key to new treatments for leukemia, a kind of cancer that attacks the blood.
The research, supported by the National Science Foundation, has revealed a previously unknown relationship between a protein in the eggs of a marine mollusk and a protein on the outside of human white blood cells. The work is published in the November issue of Nature Structural Biology.
The egg protein is from the California sea snail, Aplysia californica, an animal used by biologists to study the process of fertilization. The details of the events that occur at the molecular level when a sperm cell joins with an egg are often the same throughout the animal kingdom, including in humans. One of the first events is that a flood of calcium ions is released as a signal to the egg to prepare to begin dividing. The flood of ions is controlled by a regulatory molecule, a sort of molecular switch, termed a secondary messenger.
The secondary messenger is synthesized inside the egg from the building blocks of DNA. The synthesis reaction requires a specialized protein, known as ADP ribosyl cyclase. It is this protein that has been studied by the researchers at Scripps. By preparing crystals of the protein and scattering x-rays off them, a three-dimensional image has been reconstructed. The image reveals that two of the molecules combine together to create a hole, or molecular cavity, between the proteins. Inside this cavity the protein traps the DNA building blocks and rearranges their pattern of chemical bonds to synthesize the messenger.
In leukemia, white blood cells have a signaling protein, called CD38, which in normal cells is only present in early stages of their development. Because a CD38 molecule has a remarkable similarity to the cyclase protein, Stout and his collaborators think that CD38 molecules also pair up to create an internal cavity. However, unlike cyclase, CD38 has a tail reaching across the cell membrane, providing a means for it to transmit signals to the inside of white blood cells. "By modifying the chemical bonds in molecules outside the cell, the size and shape of the protein cavity may be changed, and this effect can be transmitted across the cell membrane by the attached tail," explains Kamal Shukla, program director in NSF's division of molecular and cellular biosciences, which funded Stout's research.
The Scripps researchers hope that drugs targeted toward the cavity in CD38 could be used to alter signal transmission and allow the immune system to eliminate leukemia cells.
Cheryl L. Dybas, NSF (703) 292-8070 firstname.lastname@example.org
Kamal Shukla, NSF (703) 292-7131 email@example.com
The National Science Foundation (NSF) is an independent federal agency that supports fundamental research and education across all fields of science and engineering. In fiscal year (FY) 2012, its budget was $7.0 billion. NSF funds reach all 50 states through grants to nearly 2,000 colleges, universities and other institutions. Each year, NSF receives about 50,000 competitive requests for funding, and makes about 11,500 new funding awards. NSF also awards about $593 million in professional and service contracts yearly.
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