Biochemical Analysis Leads to Improved Orthogonal Bioluminescent Tools
© 2023 The Authors. ChemBioChem published by Wiley-VCH GmbH..
Engineered luciferase-luciferin pairs have expanded the number of cellular targets that can be visualized in tandem. While light production relies on selective processing of synthetic luciferins by mutant luciferases, little is known about the origin of selectivity. The development of new and improved pairs requires a better understanding of the structure-function relationship of bioluminescent probes. In this work, we report a biochemical approach to assessing and optimizing two popular bioluminescent pairs: Cashew/d-luc and Pecan/4'-BrLuc. Single mutants derived from Cashew and Pecan revealed key residues for selectivity and thermal stability. Stability was further improved through a rational addition of beneficial residues. In addition to providing increased stability, the known stabilizing mutations surprisingly also improved selectivity. The resultant improved pair of luciferases are >100-fold selective for their respective substrates and highly thermally stable. Collectively, this work highlights the importance of mechanistic insight for improving bioluminescent pairs and provides significantly improved Cashew and Pecan enzymes which should be immediately suitable for multicomponent imaging applications.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2023 |
---|---|
Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:24 |
---|---|
Enthalten in: |
Chembiochem : a European journal of chemical biology - 24(2023), 6 vom: 14. März, Seite e202200726 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Williams, Sierra J [VerfasserIn] |
---|
Links: |
---|
Anmerkungen: |
Date Completed 16.03.2023 Date Revised 15.03.2024 published: Print-Electronic Citation Status MEDLINE |
---|
doi: |
10.1002/cbic.202200726 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM351036822 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM351036822 | ||
003 | DE-627 | ||
005 | 20240315232606.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231226s2023 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1002/cbic.202200726 |2 doi | |
028 | 5 | 2 | |a pubmed24n1330.xml |
035 | |a (DE-627)NLM351036822 | ||
035 | |a (NLM)36592373 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Williams, Sierra J |e verfasserin |4 aut | |
245 | 1 | 0 | |a Biochemical Analysis Leads to Improved Orthogonal Bioluminescent Tools |
264 | 1 | |c 2023 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 16.03.2023 | ||
500 | |a Date Revised 15.03.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a © 2023 The Authors. ChemBioChem published by Wiley-VCH GmbH. | ||
520 | |a Engineered luciferase-luciferin pairs have expanded the number of cellular targets that can be visualized in tandem. While light production relies on selective processing of synthetic luciferins by mutant luciferases, little is known about the origin of selectivity. The development of new and improved pairs requires a better understanding of the structure-function relationship of bioluminescent probes. In this work, we report a biochemical approach to assessing and optimizing two popular bioluminescent pairs: Cashew/d-luc and Pecan/4'-BrLuc. Single mutants derived from Cashew and Pecan revealed key residues for selectivity and thermal stability. Stability was further improved through a rational addition of beneficial residues. In addition to providing increased stability, the known stabilizing mutations surprisingly also improved selectivity. The resultant improved pair of luciferases are >100-fold selective for their respective substrates and highly thermally stable. Collectively, this work highlights the importance of mechanistic insight for improving bioluminescent pairs and provides significantly improved Cashew and Pecan enzymes which should be immediately suitable for multicomponent imaging applications | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a Research Support, U.S. Gov't, Non-P.H.S. | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a biochemical characterization | |
650 | 4 | |a bioluminescence | |
650 | 4 | |a luciferase | |
650 | 4 | |a luciferin | |
650 | 4 | |a thermostability | |
650 | 7 | |a Firefly Luciferin |2 NLM | |
650 | 7 | |a 5TBB02N29K |2 NLM | |
650 | 7 | |a Luciferases |2 NLM | |
650 | 7 | |a EC 1.13.12.- |2 NLM | |
650 | 7 | |a Luciferins |2 NLM | |
700 | 1 | |a Gewing-Mullins, Jordan A |e verfasserin |4 aut | |
700 | 1 | |a Lieberman, Whitney K |e verfasserin |4 aut | |
700 | 1 | |a Kolbaba-Kartchner, Bethany |e verfasserin |4 aut | |
700 | 1 | |a Iqbal, Reema |e verfasserin |4 aut | |
700 | 1 | |a Burgess, Hana M |e verfasserin |4 aut | |
700 | 1 | |a Colee, Clair M |e verfasserin |4 aut | |
700 | 1 | |a Ornelas, Marya Y |e verfasserin |4 aut | |
700 | 1 | |a Reid-McLaughlin, Edison S |e verfasserin |4 aut | |
700 | 1 | |a Mills, Jeremy H |e verfasserin |4 aut | |
700 | 1 | |a Prescher, Jennifer A |e verfasserin |4 aut | |
700 | 1 | |a Leconte, Aaron M |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Chembiochem : a European journal of chemical biology |d 2000 |g 24(2023), 6 vom: 14. März, Seite e202200726 |w (DE-627)NLM117153788 |x 1439-7633 |7 nnns |
773 | 1 | 8 | |g volume:24 |g year:2023 |g number:6 |g day:14 |g month:03 |g pages:e202200726 |
856 | 4 | 0 | |u http://dx.doi.org/10.1002/cbic.202200726 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 24 |j 2023 |e 6 |b 14 |c 03 |h e202200726 |