Väitös (kemia): MSc Lange Yakubu Saleh
Aika
10.5.2024 klo 12.00 - 16.00
MSc Lange Yakubu Saleh esittää väitöskirjansa ”Organomercury oligonucleotides as artificial ribonucleases” julkisesti tarkastettavaksi Turun yliopistossa perjantaina 10.05.2024 klo 12.00 (Turun yliopisto, Päärakennus, Tauno Nurmela -sali, Turku).
Yleisön on mahdollista osallistua väitökseen myös etäyhteyden kautta: https://utu.zoom.us/j/65239858781 (meeting ID 652 3985 8781, salasana 766440).
Vastaväittäjänä toimii professori Roger Strömberg (Karoliininen instituutti, Ruotsi) ja kustoksena professori Tuomas Lönnberg (Turun yliopisto). Tilaisuus on englanninkielinen. Väitöksen alana on kemia.
Väitöskirja yliopiston julkaisuarkistossa: https://urn.fi/URN:ISBN:978-951-29-9665-0
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Tiivistelmä väitöstutkimuksesta:
Traditional methods to target specific RNA sequences for degradation involve antisense oligonucleotides (ASOs), which have long relied on the natural catalytic activity of RNase H. However, integrating chemical modifications into ASOs for improved cellular delivery and stability has posed significant challenges. Striking the delicate balance between enhancing functionality while preserving RNase H recruitment has proven elusive, hindering optimal therapeutic efficacy.
Artificial Ribonucleases (aRNases) are designed to ively cleave RNA sequences, mirroring the function of natural ribonucleases but tailored for specific applications. These synthetic counterparts effectively cleave phosphodiester bonds in RNA molecules, enabling diverse applications, including targeted degradation of specific RNA sequences within cells. The current leading aRNases, utilizing metal ions like Cu(II) or Zn(II) in coordination complexes, are prone to dissociation in highly diluted and metal-deficient environments, such as the intracellular medium. However, aRNases with catalytic metal ions bonded to carbon demonstrate resistance to dissociation even under extreme dilution. This suggests a potential to combine the stability of organic compounds with the catalytic effectiveness of metal complexes.
The research commenced with Hg (II), chosen as the catalytic metal ion due to its hydrolytic stability and the ready availability of arylmercury complexes. Kinetic studies conducted across varied pH ranges showed the efficacy of Hg (II) and arylmercury complexes in catalyzing the cleavage of RNA model molecules. Encouraged by these results, two oligonucleotide conjugates, each featuring distinct 5´-terminal organomercury moieties were prepared via either direct mercuration in solution or oximation with an organomercury aldehyde on solid support. Both conjugates exhibited sequence-specific aRNase activity, significantly accelerating reactions compared to catalyst-free conditions and thus paving the way for diverse applications in targeted RNA degradation within cells.
Yleisön on mahdollista osallistua väitökseen myös etäyhteyden kautta: https://utu.zoom.us/j/65239858781 (meeting ID 652 3985 8781, salasana 766440).
Vastaväittäjänä toimii professori Roger Strömberg (Karoliininen instituutti, Ruotsi) ja kustoksena professori Tuomas Lönnberg (Turun yliopisto). Tilaisuus on englanninkielinen. Väitöksen alana on kemia.
Väitöskirja yliopiston julkaisuarkistossa: https://urn.fi/URN:ISBN:978-951-29-9665-0
***
Tiivistelmä väitöstutkimuksesta:
Traditional methods to target specific RNA sequences for degradation involve antisense oligonucleotides (ASOs), which have long relied on the natural catalytic activity of RNase H. However, integrating chemical modifications into ASOs for improved cellular delivery and stability has posed significant challenges. Striking the delicate balance between enhancing functionality while preserving RNase H recruitment has proven elusive, hindering optimal therapeutic efficacy.
Artificial Ribonucleases (aRNases) are designed to ively cleave RNA sequences, mirroring the function of natural ribonucleases but tailored for specific applications. These synthetic counterparts effectively cleave phosphodiester bonds in RNA molecules, enabling diverse applications, including targeted degradation of specific RNA sequences within cells. The current leading aRNases, utilizing metal ions like Cu(II) or Zn(II) in coordination complexes, are prone to dissociation in highly diluted and metal-deficient environments, such as the intracellular medium. However, aRNases with catalytic metal ions bonded to carbon demonstrate resistance to dissociation even under extreme dilution. This suggests a potential to combine the stability of organic compounds with the catalytic effectiveness of metal complexes.
The research commenced with Hg (II), chosen as the catalytic metal ion due to its hydrolytic stability and the ready availability of arylmercury complexes. Kinetic studies conducted across varied pH ranges showed the efficacy of Hg (II) and arylmercury complexes in catalyzing the cleavage of RNA model molecules. Encouraged by these results, two oligonucleotide conjugates, each featuring distinct 5´-terminal organomercury moieties were prepared via either direct mercuration in solution or oximation with an organomercury aldehyde on solid support. Both conjugates exhibited sequence-specific aRNase activity, significantly accelerating reactions compared to catalyst-free conditions and thus paving the way for diverse applications in targeted RNA degradation within cells.
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