TY - JOUR
T1 - Simple enzymatic incorporation of 2′OMeU nucleotide at the end of the poly-A tail for enhancement of the mRNA stability and protein expression
AU - Alom, Kazi Morshed
AU - Asa, Tasnima Alam
AU - Seo, Young Jun
PY - 2024/10/18
Y1 - 2024/10/18
N2 - This study focused on the efficient post-transcriptional incorporation of a modified nucleoside at the end of the poly-A tail of mRNA. The modified mRNA was obtained in high yield and served to enhance protein expression. Utilizing poly-U polymerase, our method successfully enabled a single 2′OMeU residue to be incorporated into mRNA, which unexpectedly provided significant stabilization, even with only a single incorporation, to enhance the resistance of mRNA to degradation by cellular exonuclease. This stabilization effect allowed the mRNA to remain viable within the cell for an extended period to ultimately increase the translation efficiency at least 3-fold. This approach to mRNA modification at the 3′ end with a single 2′OMeU residue, by utilizing a straightforward tailing method, surpasses other ligation methods in terms of mRNA modification efficiency. Collectively, our results highlight the potential of this method to significantly advance the development of highly effective mRNA-based therapies in the future.
AB - This study focused on the efficient post-transcriptional incorporation of a modified nucleoside at the end of the poly-A tail of mRNA. The modified mRNA was obtained in high yield and served to enhance protein expression. Utilizing poly-U polymerase, our method successfully enabled a single 2′OMeU residue to be incorporated into mRNA, which unexpectedly provided significant stabilization, even with only a single incorporation, to enhance the resistance of mRNA to degradation by cellular exonuclease. This stabilization effect allowed the mRNA to remain viable within the cell for an extended period to ultimately increase the translation efficiency at least 3-fold. This approach to mRNA modification at the 3′ end with a single 2′OMeU residue, by utilizing a straightforward tailing method, surpasses other ligation methods in terms of mRNA modification efficiency. Collectively, our results highlight the potential of this method to significantly advance the development of highly effective mRNA-based therapies in the future.
UR - http://www.scopus.com/inward/record.url?scp=85204894787&partnerID=8YFLogxK
U2 - 10.1021/acschembio.4c00420
DO - 10.1021/acschembio.4c00420
M3 - Article
C2 - 39301931
AN - SCOPUS:85204894787
SN - 1554-8929
VL - 19
SP - 2206
EP - 2213
JO - ACS Chemical Biology
JF - ACS Chemical Biology
IS - 10
ER -