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Identifying Molecules as Biosignatures with Assembly Theory and Mass SpectrometryThe search for evidence of life elsewhere in the universe is hard because it is not obvious what signatures are unique to life. Here we postulate that complex molecules found in high abundance are universal biosignatures as they cannot form by chance. To explore this, we developed the first intrinsic measure of molecular complexity that can be experimentally determined, and this is based upon a new approach called assembly theory which gives the molecular assembly number (MA) of a given molecule. MA allows us to compare the intrinsic complexity of molecules using the minimum number of steps required to construct the molecular graph starting from basic objects, and a probabilistic model shows how the probability of any given molecule forming randomly drops dramatically as its MA increases. To map chemical space, we calculated the MA of ca. 2.5 million compounds, and collected data which showed the complexity of a molecule can be experimentally determined by using three independent techniques including infra-red spectroscopy, nuclear magnetic resonance, and by fragmentation in a mass spectrometer, and this data has an excellent corelation with the values predicted from our assembly theory. We then set out to see if this approach could allow us to identify molecular biosignatures with a set of diverse samples from around the world, outer space, and the laboratory including prebiotic soups. The results show that there is a non-living to living threshold in MA complexity and the higher the MA for a given molecule, the more likely that it had to be produced by a biological process. This work demonstrates it is possible to use this approach to build a life detection instrument that could be deployed on missions to extra-terrestrial locations to detect biosignatures, map the extent of life on Earth, and be used as a molecular complexity scale to quantify the constraints needed to direct prebiotically plausible processes in the laboratory. Such an approach is vital if we are going to find new life elsewhere in the universe or create de-novo life in the lab.
Document ID
20210016990
Acquisition Source
Goddard Space Flight Center
Document Type
Accepted Manuscript (Version with final changes)
Authors
Stuart M Marshall
(University of Glasgow Glasgow, United Kingdom)
Cole Mathis
(University of Glasgow Glasgow, United Kingdom)
Emma Carrick
(University of Glasgow Glasgow, United Kingdom)
Graham Keenan
(University of Glasgow Glasgow, United Kingdom)
Geoffrey J T Cooper
(University of Glasgow Glasgow, United Kingdom)
Heather Graham
(Catholic University of America Washington D.C., District of Columbia, United States)
Jessica R Bame
(University of Glasgow Glasgow, United Kingdom)
Matthew Craven
(University of Glasgow Glasgow, United Kingdom)
Nicola L Bell
(University of Glasgow Glasgow, United Kingdom)
Piotr S Gromski
(University of Glasgow Glasgow, United Kingdom)
Marcel Swart
(University of Girona Girona, Spain)
Douglas G Moore
(Arizona State University Tempe, Arizona, United States)
Sara I Walker
(Arizona State University Tempe, Arizona, United States)
Leroy Cronin
(University of Glasgow Glasgow, United Kingdom)
Date Acquired
June 4, 2021
Publication Date
May 24, 2021
Publication Information
Publication: Nature Communications
Publisher: Springer Nature
Volume: 12
Issue: 3033 (2021)
Issue Publication Date: May 24, 2021
e-ISSN: 2041-1723
URL: https://www.nature.com/articles/s41467-021-23258-x
Subject Category
Exobiology
Funding Number(s)
WBS: 811073.02.12.04.49
Distribution Limits
Public
Copyright
Portions of document may include copyright protected material.
Technical Review
External Peer Committee
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