Scientists identify new details of biochemical interactions necessary for cell division
Upton, NY and Cold Spring Harbor, NY — Building on earlier work exploring the complex choreography by which intricate cellular proteins interact with and copy DNA prior to cell division, scientists at the U.S. Department of Energy’s Brookhaven National Laboratory and collaborators at Cold Spring Harbor Laboratory (CSHL) and elsewhere have captured a key step—molecular images showing how the enzyme that unwinds the DNA double helix gets drawn to and wrapped around its target.
Details of the research, published online today in the Nature Structural & Molecular Biology, enhance understanding of an essential biological process and may suggest ways for stopping cell division when it goes awry.
“This was truly collaborative work where molecular biology expertise from Christian Speck’s lab at Imperial College, London, Bruce Stillman’s group at Cold Spring Harbor Laboratory, and the cryo-electron microscopy expertise at Brookhaven were all essential,” said Huilin Li, a biologist at Brookhaven Lab and Stony Brook University and a lead author on the paper.
“Our work is aimed at understanding the molecular details and mechanism of DNA replication at a fundamental level,” said Li, “But our findings could have important implications, possibly pointing to new ways to fight cancer, because irregularities in DNA duplication and uncontrolled cell division are hallmarks of the disease.”
The current research picks up where a study conducted last year left off. That research determined the structure of a piece of protein machinery called the “origin recognition complex” (ORC), which identifies and binds to DNA-replication “start” sites. When joined by a replication initiation factor, the ORC undergoes conformational changes that set in motion the whole replication process. The new study reveals how this previous structure recruits and interacts with the enzyme that eventually unwinds the DNA double helix into two separate strands.
“What we’ve uncovered in this study was a kind of missing link—what happens to this helicase enzyme before it encircles the DNA and starts unwinding the two strands,” Li said.
Catching the molecular machinery in action is no simple task. Intermediate protein structures exist on fleeting timescales, and the interactions take place at the atomic level. Researchers working in Speck and Stillman’s labs used tools of molecular biology and biochemistry to slow down the process. They purified and then remixed together pieces of the protein puzzle (including the origin recognition complex, the replication initiator, the core of the helicase, and other components) and a slow-acting energy agent so the energy-requiring reaction is unable to proceed to completion. Like dancers paused in place by a sudden stop of music, the molecular components “froze” partway through the helicase recruitment/assembly process.
Jingchuan Sun at Brookhaven then literally froze the samples, embedding them in ice, and took tens of thousands of pictures with a cryo-electron microscope. He then used computer software to reconstruct the 3-D structure from the 2-D electron microscope pictures. “The 3-D reconstruction gave us a snapshot of the elusive intermediate structure,” Sun said.
Comparing the new structure (components of the helicase bound to the origin recognition complex) with the structures of the ORC produced last year revealed conformational changes. Binding of the helicase core components appears to shift the ORC into a spiral conformation that closely matches the spiral shape of double-stranded DNA.
“This shape-shifting of the ORC appears to be an important step in facilitating binding of the ring-shaped helicase to the DNA,” Sun said.
The scientists also note that the spiral-shaped ORC is similar to another spiral protein complex that loads a different ring structure to keep DNA polymerase enzymes from falling off the DNA while synthesizing new strands to complete the replication process.
“Both of these complexes were discovered in the Stillman lab nearly two decades ago. It’s rewarding to see now that these two energy-requiring protein machines form similar spiral structures to recruit and load their ‘cargo’ onto DNA for these crucial steps in the replication process,” said Li.
Said co-author Stillman, who is president of Cold Spring Harbor Laboratory in addition to leading an active research lab at CSHL: “It is amazing how two seemingly separate steps in the process of duplicating our genome are so similar in their biochemical mechanism. Using the advanced microscope facilities at Brookhaven Lab has once again generated a surprising result.”
This release was written by Brookhaven National Laboratory and appears here with its permission.
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This research was funded by the National Institutes of Health (GM45436, GM74985), the U.K. Medical Research Council, the Japan Society for the Promotion of Science, and the Uehara Memorial Foundation.
About Brookhaven National Laboratory
Brookhaven National Laboratory is a multipurpose research institution funded by the U.S. Department of Energy. Located on Long Island, NY, Brookhaven operates large-scale facilities for studies in physics, chemistry, biology, medicine, applied science, and advanced technology. The Laboratory’s almost 3,000 scientists, engineers, and support staff are joined each year by more than 5,000 visiting researchers from around the world.
Founded in 1890, Cold Spring Harbor Laboratory has shaped contemporary biomedical research and education with programs in cancer, neuroscience, plant biology and quantitative biology. Home to eight Nobel Prize winners, the private, not-for-profit Laboratory employs 1,100 people including 600 scientists, students and technicians. The Meetings & Courses Program annually hosts more than 12,000 scientists. The Laboratory’s education arm also includes an academic publishing house, a graduate school and the DNA Learning Center with programs for middle and high school students and teachers. For more information, visit www.cshl.edu