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PubMed Publications| Keyword search (4,163 papers available) |  |
"Jiang J" Authored Publications:
| Title | Authors | PubMed ID | |
|---|---|---|---|
| 1 | High selectivity framework polymer membranes chemically tuned towards fast anion conduction | Fang J; Zhang G; Goulet MA; Zuo P; Zhou Y; Li H; Jiang J; Guiver MD; Yang Z; Xu T; | 40188171 ENCS |
| 2 | Enhanced binding of guanylated poly(A) RNA by the LaM domain of LARP1 | Kozlov G; Jiang J; Rutherford T; Noronha AM; Wilds CJ; Gehring K; | 39016322 CHEMBIOCHEM |
| 3 | Biomolecules incorporated in halide perovskite nanocrystals: synthesis, optical properties, and applications | Aminzare M; Jiang J; Mandl GA; Mahshid S; Capobianco JA; Dorval Courchesne NM; | 36722934 CHEMBIOCHEM |
| 4 | Structural basis of 3'-end poly(A) RNA recognition by LARP1 | Kozlov G; Mattijssen S; Jiang J; Nyandwi S; Sprules T; Iben JR; Coon SL; Gaidamakov S; Noronha AM; Wilds CJ; Maraia RJ; Gehring K; | 35979957 CHEMBIOCHEM |
| Title: | Enhanced binding of guanylated poly(A) RNA by the LaM domain of LARP1 | ||||
| Authors: | Kozlov G, Jiang J, Rutherford T, Noronha AM, Wilds CJ, Gehring K | ||||
| Link: | https://pubmed.ncbi.nlm.nih.gov/39016322/ | ||||
| DOI: | 10.1080/15476286.2024.2379121 | ||||
| Publication: | RNA biology | ||||
| Keywords: | LARP, La-related protein; LARP1, La-related protein 1; LaM, La motif; guanylation; phosphorothioate; poly(a) tail; | ||||
| PMID: | 39016322 | Category: | Date Added: | 2024-07-17 | |
| Dept Affiliation: |
CHEMBIOCHEM
1 Department of Biochemistry, McGill University, Montréal, Quebec, Canada. 2 Centre de recherche en biologie structurale, McGill University, Montréal, Quebec, Canada. 3 Department of Chemistry and Biochemistry, Concordia University, Montréal, Quebec, Canada. |
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Description: |
La-related proteins (LARPs) are a family of RNA-binding proteins that share a conserved La motif (LaM) domain. LARP1 plays a role in regulating ribosomal protein synthesis and stabilizing mRNAs and has a unique structure without an RNA binding RRM domain adjoining the LaM domain. In this study, we investigated the physical basis for LARP1 specificity for poly(A) sequences and observed an unexpected bias for sequences with single guanines. Multiple guanine substitutions did not increase the affinity, demonstrating preferential recognition of singly guanylated sequences. We also observed that the cyclic di-nucleotides in the cCAS/STING pathway, cyclic-di-GMP and 3',3'-cGAMP, bound with sub-micromolar affinity. Isothermal titration measurements were complemented by high-resolution crystal structures of the LARP1 LaM with six different RNA ligands, including two stereoisomers of a phosphorothioate linkage. The selectivity for singly substituted poly(A) sequences suggests LARP1 may play a role in the stabilizing effect of poly(A) tail guanylation. [Figure: see text]. |
