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Electronic Life-detection Instrument for Enceladus/Europa (ELIE)
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  • Christopher Carr,
  • Daniel Duzdevich,
  • Jack Szostak,
  • Sam Lee,
  • Masateru Taniguchi,
  • Takahito Ohshiro,
  • Yuki Komoto,
  • Gary Ruvkun,
  • Jason Soderblom,
  • Maria Zuber
Christopher Carr
Georgia Institute of Technology Main Campus

Corresponding Author:[email protected]

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Daniel Duzdevich
Howard Hughes Medical Institute
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Jack Szostak
Howard Hughes Medical Institute
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Sam Lee
Massachusetts Institute of Technology
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Masateru Taniguchi
Osaka University
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Takahito Ohshiro
Osaka University
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Yuki Komoto
Osaka University
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Gary Ruvkun
Massachusetts General Hospital
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Jason Soderblom
MIT
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Maria Zuber
Massachusetts Inst Tech
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Abstract

Habitable regions of Europa may include a subsurface ocean and transient liquid environments within its icy shell. Ocean-surface communication may occur on 1–2 million-year (My) timescales or even more rapidly in chaos regions. Any ice-entombed organisms could remain viable at near-surface depths (10–100 cm) over 1–10 ky. The proposed Europa Lander will target samples at depths >10 cm, potentially enabling recovery of viable organisms if sampling conditions are ideal. Any life there would likely represent a separate genesis event from Earth life. Life detection approaches should therefore not only target life as we know it (contamination, common physicochemistry), but also as we don’t know it, to lower the risk of false negatives. We propose to target prebiotic, ancient, or extant life using a novel fully-electronic single-molecule detection strategy. Now in early development (PICASSO), the Electronic Life-detection Instrument for Enceladus/Europa (ELIE) instrument will utilize quantum electron tunneling between nanogap electrodes to interrogate the electronic structure of single molecules. Nanogaps are formed by breaking a gold nanowire embedded on a silicon chip. Bending is then used to control the gap size in the sub-nanometer regime. A molecule can be identified by its characteristic conductance and interaction time as a function of gap size. This technology can detect and distinguish among amino acids, and detect RNA and DNA bases and short base sequences. The extrapolated limit of detection for single amino acids is ~200 ppt after 5 min of sampling (~1 pMol/g). Integrating upfront separation methods will enhance specificity and sensitivity. Our lab-bench prototype integrates a nanogap chip, low-noise amplifier, and a laptop for data processing. We target a ~1 kg flight instrument mass. ELIE will be able to measure two key biosignatures: the amino acid complexity distribution, and charged informational polymers, through to be universal for aqueous based life.