N-Acetylaspartate Is an Important Brain Osmolyte
Overview
Molecular Biology
Authors
Affiliations
Most of the human diseases related to various proteopathies are confined to the brain, which leads to the development of various forms of neurological disorders. The human brain consists of several osmolytic compounds, such as N-Acetylaspartate (NAA), myo-inositol (mI), glutamate (Glu), glutamine (Gln), creatine (Cr), and choline-containing compounds (Cho). Among these osmolytes, the level of NAA drastically decreases under neurological conditions, and, hence, NAA is considered to be one of the most widely accepted neuronal biomarkers in several human brain disorders. To date, no data are available regarding the effect of NAA on protein stability, and, therefore, the possible effect of NAA under proteopathic conditions has not been fully uncovered. To gain an insight into the effect of NAA on protein stability, thermal denaturation and structural measurements were carried out using two model proteins at different pH values. The results indicate that NAA increases the protein stability with an enhancement of structure formation. We also observed that the stabilizing ability of NAA decreases in a pH-dependent manner. Our study indicates that NAA is an efficient protein stabilizer at a physiological pH.
The Impact of HIV on Early Brain Aging-A Pathophysiological (Re)View.
Lazar M, Moroti R, Barbu E, Chitu-Tisu C, Tiliscan C, Erculescu T J Clin Med. 2024; 13(23).
PMID: 39685490 PMC: 11642420. DOI: 10.3390/jcm13237031.
Childhood Obesity, Hypothalamic Inflammation, and the Onset of Puberty: A Narrative Review.
Tzounakou A, Stathori G, Paltoglou G, Valsamakis G, Mastorakos G, Vlahos N Nutrients. 2024; 16(11).
PMID: 38892653 PMC: 11175006. DOI: 10.3390/nu16111720.
Understanding the Modulation of α-Synuclein Fibrillation by -Acetyl Aspartate: A Brain Metabolite.
Khan T, Waseem R, Shahid M, Ansari J, Hassan M, Shamsi A ACS Omega. 2024; 9(10):12262-12271.
PMID: 38496993 PMC: 10938311. DOI: 10.1021/acsomega.4c00595.
Elsaid S, Rubin-Kahana D, Kloiber S, Kennedy S, Chavez S, Le Foll B Int J Mol Sci. 2022; 23(9).
PMID: 35563145 PMC: 9105768. DOI: 10.3390/ijms23094754.
Hu B, Das P, Lv X, Shi M, Aa J, Wang K mSystems. 2022; 7(3):e0021822.
PMID: 35481347 PMC: 9239139. DOI: 10.1128/msystems.00218-22.