Bichromatic spectrophotometry determinations were performed on Whatman chromatographic paper disks impregnated with rRNA solutions of different concentrations, at ionic strengths ranging from nearly 0 to 1.4 M. The disks consisted of cellulose, either native or modified (by grafting of carboxymethyl, phosphate, Ecteola or DEAE groups, or by loading with silica gel). The results demonstrate that: 1) there is a positive correlation between the absorbance enhancement by multiple light scattering and the nearness of the nucleic acid molecules in relation to the surface of cellulose fibrils; b) the action on absorbance of ionic strength and of other physical factors differs in terms of the electric charges and of the exposure of other groups that may interact with nucleic acids through hydrogen bonds or Van der Waals forces.
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J Inflamm Res
January 2025
Department of Hepatobiliary Surgery, The First People's Hospital of Zhaoqing, Zhaoqing City, Guangdong Province, People's Republic of China.
Background: Myocardial ischemia/reperfusion (I/R) injury significantly impacts the recovery of ischemic heart disease patients. Non-coding RNAs, including miRNAs, have been increasingly recognized for their roles in regulating cardiomyocyte responses to hypoxia/reoxygenation (H/R) injury. miR-181c-5p, in particular, has been implicated in inflammatory and apoptotic processes, suggesting its potential involvement in exacerbating cellular damage.
View Article and Find Full Text PDFPhilos Trans R Soc Lond B Biol Sci
January 2025
Division of Life Science and State Key Laboratory of Molecular Neuroscience, The Hong Kong University of Science and Technology, Hong Kong, China.
Bacterial extracellular vesicles (EVs) are vesicles secreted by bacteria into the extracellular environment. Containing DNA, RNA and proteins, EVs are implicated to mediate intercellular communications. The marine cyanobacterium , the most abundant photosynthetic organism in marine ecosystems, has been shown to generate EVs continuously during cell growth.
View Article and Find Full Text PDFAnal Chem
January 2025
Synthetic Molecule Analytical Chemistry, Genentech Inc., South San Francisco, California 94080, United States.
Accurate characterization of therapeutic RNA, including purity and identity, is critical in drug discovery and development. Here, we utilize denaturing and non-denaturing chromatography for the analysis of ∼25 kDa divalent small interfering RNA (di-siRNA), which comprises a complex 2:1 triplex structure. Ion pair reversed-phase (IPRP) liquid chromatography (LC) experiments with UV absorbance and mass spectrometry (MS) showcase a single denaturing LC method for identity confirmation, impurity profiling, and sequencing with automated MS data interpretation.
View Article and Find Full Text PDFBiosens Bioelectron
January 2025
Jinling Clinical Medical College, Nanjing University of Chinese Medicine, 210002, Nanjing, Jiangsu Province, China; Department of Orthopedics, Jinling Hospital, Affiliated Hospital of Medical School, Nanjing University, 210002, Nanjing, Jiangsu Province, China; Division of Trauma and Acute Care Surgery, Department of Surgery, Jinling Hospital, Jinling Clinical Medical College, Nanjing University of Chinese Medicine, 210002, Nanjing, Jiangsu Province, China. Electronic address:
The rapid and reliable diagnosis of methicillin-resistant Staphylococcus aureus (MRSA) is essential for preventing the spread of MRSA infections and guiding therapeutic strategies. However, there is still a huge challenge in further simplifying MRSA detection procedures and improving detection selectivity to reduce false-positive results. In this study, we developed a derivative CRISPR-associated protein 9/CRISPR-derived RNA Linked Immunological Assay (dCLISA) for the sensitive and specific detection of MRSA.
View Article and Find Full Text PDFBMC Microbiol
January 2025
Microbial Chemistry Department, Biotechnology Research Institute, National Research Center, Dokki, Giza, Egypt.
The red pigment was recovered from the S. phaeolivaceus GH27 isolate, which was molecularly identified using 16S rRNA gene sequencing and submitted to GenBank as OQ145635.1.
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