Engineering indel and substitution variants of diverse and ancient enzymes using Graphical Representation of Ancestral Sequence Predictions (GRASP)

Medientyp: E-Artikel

Titel: Engineering indel and substitution variants of diverse and ancient enzymes using Graphical Representation of Ancestral Sequence Predictions (GRASP)

Beteiligte: Foley, Gabriel; Mora, Ariane; Ross, Connie M.; Bottoms, Scott; Sützl, Leander; Lamprecht, Marnie L.; Zaugg, Julian; Essebier, Alexandra; Balderson, Brad; Newell, Rhys; Thomson, Raine E. S.; Kobe, Bostjan; Barnard, Ross T.; Guddat, Luke; Schenk, Gerhard; Carsten, Jörg; Gumulya, Yosephine; Rost, Burkhard; Haltrich, Dietmar; Sieber, Volker; Gillam, Elizabeth M. J.; Bodén, Mikael

Erschienen: Public Library of Science (PLoS), 2022

Sprache: Englisch

DOI: 10.1371/journal.pcbi.1010633

ISSN: 1553-7358

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Beschreibung: Ancestral sequence reconstruction is a technique that is gaining widespread use in molecular evolution studies and protein engineering. Accurate reconstruction requires the ability to handle appropriately large numbers of sequences, as well as insertion and deletion (indel) events, but available approaches exhibit limitations. To address these limitations, we developed Graphical Representation of Ancestral Sequence Predictions (GRASP), which efficiently implements maximum likelihood methods to enable the inference of ancestors of families with more than 10,000 members. GRASP implements partial order graphs (POGs) to represent and infer insertion and deletion events across ancestors, enabling the identification of building blocks for protein engineering. To validate the capacity to engineer novel proteins from realistic data, we predicted ancestor sequences across three distinct enzyme families: glucose-methanol-choline (GMC) oxidoreductases, cytochromes P450, and dihydroxy/sugar acid dehydratases (DHAD). All tested ancestors demonstrated enzymatic activity. Our study demonstrates the ability of GRASP (1) to support large data sets over 10,000 sequences and (2) to employ insertions and deletions to identify building blocks for engineering biologically active ancestors, by exploring variation over evolutionary time.

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