London: According to a new study by Nick Lane and colleagues at University College London, UK, a straightforward two-carbon molecule may have been a key participant in the evolution of metabolism before the appearance of cells. The discovery may shed light on the earliest phases of prebiotic biochemistry and offer an explanation for how ATP came to be the common energy source for all living things in cells today.
All cells employ the energy intermediary ATP or adenosine triphosphate. When phosphate is added to ADP (adenosine diphosphate) to create ATP, energy is acquired during cellular respiration; the cleavage of that phosphate releases energy to fuel most cellular processes. While convincing models do allow for the prebiotic formation of the ATP skeleton without power from already-formed ATP, they also suggest ATP was likely quite scarce and that some other compound may have played a key role in the conversion of ADP to ADP at this stage of evolution. However, building ATP's complex chemical structure from scratch is energy intensive and requires six separate ATP-driven steps.
Acetyl phosphate (AcP), a two-carbon molecule that currently serves as a metabolic intermediary in both bacteria and archaea, was regarded by Lane and colleagues as the most likely option. After the discovery that AcP can convert ADP to ATP in the presence of iron ions, many unanswered questions remained, such as whether other small molecules might also be effective, whether AcP is specific for ADP or whether it could also convert the diphosphates of other nucleosides (such as guanosine or cytosine), and whether iron is the only catalyst that can catalyse ADP phosphorylation in water.
The authors looked into each of these issues in their most recent study. They investigated the ability of various ions and minerals to catalyse ATP synthesis in water; none were even close to as effective as iron, based on evidence and speculations about the chemical state of the Earth before life originated. They next put a panel of several tiny organic molecules to the test to see how well they could phosphorylate ADP; none were as successful as AcP, and only one other compound (carbamoyl phosphate) showed any appreciable activity. They concluded by demonstrating that none of the other nucleoside diphosphates took a phosphate from AcP.
The authors propose a mechanistic explanation for the specificity of the ADP/AcP/iron reaction using these findings in conjunction with molecular-dynamic modelling. They postulate that the iron ion's small diameter and high charge density, as well as the conformation of the intermediate, formed when the three come together, provide the "just right" geometry that enables ACP's phosphate to switch partners and form ATP.
"Our results suggest that AcP is the most plausible precursor to ATP as a biological phosphorylation," Lane says, "and that the emergence of ATP as the universal energy currency of the cell was not the result of a 'frozen accident,' but arose from the unique interactions of ADP and AcP. Over time, with the emergence of suitable catalysts, ATP could eventually displace AcP as a ubiquitous phosphate donor, and promote the polymerization of amino acids and nucleotides to form RNA, DNA and proteins."
Silvana Pinna, the lead author, says, "I reasoned that since ATP is so essential to metabolism, it might be able to synthesise it from ADP in a prebiotic environment. However, I also believed that a number of metal ion catalysts and phosphorylating agents, particularly those that are conserved in life, would be effective. The reaction's extreme selectivity in the metal ion, phosphate donor, and substrate with molecules that life still employs was a huge surprise. It's actually extremely significant for the origin of life that this occurs most effectively in water and under mild and life-supporting conditions." —ANI
