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David Patsch

Explore the profile of David Patsch including associated specialties, affiliations and a list of published articles. Areas
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Articles 7
Citations 36
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Recent Articles
1.
Patsch D, Schwander T, Voss M, Schaub D, Huppi S, Eichenberger M, et al.
Nat Chem Biol . 2024 Sep; 20(12):1662-1669. PMID: 39261644
Darwinian evolution has given rise to all the enzymes that enable life on Earth. Mimicking natural selection, scientists have learned to tailor these biocatalysts through recursive cycles of mutation, selection...
2.
Honda Malca S, Duss N, Meierhofer J, Patsch D, Niklaus M, Reiter S, et al.
Commun Chem . 2024 Feb; 7(1):46. PMID: 38418529
Semi-rational enzyme engineering is a powerful method to develop industrial biocatalysts. Profiting from advances in molecular biology and bioinformatics, semi-rational approaches can effectively accelerate enzyme engineering campaigns. Here, we present...
3.
Patsch D, Buller R
Chimia (Aarau) . 2023 Dec; 77(3):116-121. PMID: 38047813
The combinatorial composition of proteins has triggered the application of machine learning in enzyme engineering. By predicting how protein sequence encodes function, researchers aim to leverage machine learning models to...
4.
Patsch D, Eichenberger M, Voss M, Bornscheuer U, Buller R
Comput Struct Biotechnol J . 2023 Sep; 21:4488-4496. PMID: 37736300
Enzymes are potent catalysts with high specificity and selectivity. To leverage nature's synthetic potential for industrial applications, various protein engineering techniques have emerged which allow to tailor the catalytic, biophysical,...
5.
Buchler J, Honda Malca S, Patsch D, Voss M, Turner N, Bornscheuer U, et al.
Nat Commun . 2022 Jan; 13(1):371. PMID: 35042883
Late-stage functionalization of natural products offers an elegant route to create novel entities in a relevant biological target space. In this context, enzymes capable of halogenating sp carbons with high...
6.
Eichenberger M, Huppi S, Patsch D, Aeberli N, Berweger R, Dossenbach S, et al.
Angew Chem Int Ed Engl . 2021 Aug; 60(50):26080-26086. PMID: 34346556
Squalene-hopene cyclases (SHCs) have great potential for the industrial synthesis of enantiopure cyclic terpenoids. A limitation of SHC catalysis has been the enzymes' strict (S)-enantioselectivity at the stereocenter formed after...
7.
Weber D, Patsch D, Neumann A, Winkler M, Rother D
Chembiochem . 2021 Feb; 22(10):1823-1832. PMID: 33527702
Accessing aldehydes from carboxylate moieties is often a challenging task. In this regard, carboxylate reductases (CARs) are promising catalysts provided by nature that are able to accomplish this task in...