Harnessing Conformational Dynamics to Engineer New Enzymes: Prof. Lynn Kamerlin, Uppsala University

Seminar series
Other
When
Thu, Dec 10 4:00pm to 5:00pm
Where
Zoom - To acquire link email nikkie@chem.ucla.edu
Speaker Professor Lynn Kamerlin
Uppsala University
Chemistry
Description

Harnessing Conformational Dynamics to Engineer New Enzymes

Understanding how new enzyme functions evolve, either on existing scaffolds, or completely de novo on previously non-catalytic scaffolds, is of great interest both from a fundamental biochemistry perspective, and from a biotechnological perspective. Several hypotheses have been put forward to rationalize enzyme evolution, one of which is that their conformational dynamics plays an important role in facilitating the emergence of new enzyme functions.[1-3] My team and I have invested substantial research effort into understanding enzyme multifunctionality in catalytically promiscuous enzymes,[4-7] as well as the structure-function-dynamics relationships shaping the evolution of new enzyme functions, in both natural and engineered active sites.[8-12] In this talk, I will discuss recent progress in this area, and illustrate how we have engineered conformational dynamics to generate a a de novo active site capable of catalyzing a non-natural reaction,[9] and then subsequently enhanced this activity using a simple computational approach, reaching catalytic efficiency comparable to that of naturally occurring enzymes.[13]

 

[1] James & Tawfik, Trends Biochem. Sci., 2003, 28, 361. [2] Tokuriki & Tawfik, Science, 2009, 324, 203. [3] Crean et al., J. Am. Chem. Soc., 2020, 142, 11324. [4] Barrozo et al., J. Am. Chem. Soc., 2015, 137, 9061. [5] Ben-David et al., J. Mol. Biol., 2015, 427, 1359. [6] Blaha-Nelson et al., J. Am. Chem. Soc., 2017, 139, 1155. [7] Purg et al., J. Am. Chem. Soc., 2017, 139, 17533. [8] Ma et al., Chem. Sci., 2016, 7, 1415. [9] Risso et al., Nat. Commun., 2017, 8, 16113. [10] Petrović et al., ACS Catal., 2017, 6, 6188. [11] Baier et al., eLife, 2019, 8, e40789. [12] Kaltenbach et al., Nat. Chem. Biol., 2018, 14, 548. [13] Risso et al., Chem. Sci. 2020, 11, 6134.

 

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