๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

13C-NMR investigation of protein synthesis during apoptosis in human leukemic cell lines

โœ Scribed by Corey E. Scott; Foluso Adebodun


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
171 KB
Volume
181
Category
Article
ISSN
0021-9541

No coin nor oath required. For personal study only.

โœฆ Synopsis


In order to evaluate the role of protein synthesis in apoptosis, 13 C-NMR has been used to study the levels of protein synthesis in three different human leukemic cell lines in the presence and absence of dexamethasone-induced apoptosis. Measurements were done on one dexamethasone-sensitive (CEM-C7-14) and two different dexamethasone-resistant variants (CEM-4R4 and CEM-ICR27-4). The incorporation of 13 C-labeled amino acids into cellular proteins, which reflects the level of new protein synthesis, was monitored by 13 C-NMR spectroscopy. In the absence of dexamethasone, the level of protein synthesis was found to be significantly different among the three cell lines. Dexamethasone caused a significant reduction (ะฅ60 -87%) in the level of protein synthesis in dexamethasonesensitive CEM-C7-14 cells, while having no significant effect on protein synthesis in dexamethasone-resistant CEM-4R4 cells. Dexamethasone treatment caused a significant enhancement of the level of protein synthesis in the CEM-ICR27-4 cells. Synthesis of proteins was found to occur during apoptosis, albeit at a low level, suggesting a role for the synthesis of specific proteins in the mechanism of apoptosis.


๐Ÿ“œ SIMILAR VOLUMES


Localization and synthesis of acetylchol
โœ T. Fujii; T. Tsuchiya; S. Yamada; K. Fujimoto; T. Suzuki; T. Kasahara; K. Kawash ๐Ÿ“‚ Article ๐Ÿ“… 1996 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 663 KB

In order to clarify the origin of acetylcholine (ACh) in human blood, we measured the content and synthesis activity of ACh in several human leukemic cell lines. The intracellular ACh content determined by a specific and sensitive radioimmunoassay in the human leukemic T cell lines, HSB-2, MOLT-3, a

A cyclic peptide, L1AD3, induces early s
โœ Charles A. Smith; Channing L. Hinman ๐Ÿ“‚ Article ๐Ÿ“… 2004 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 278 KB

## Abstract L1AD3 is a small cyclic synthetic peptide designed to resemble the first loop of a cobra venom cytotoxin. Instead of inducing membrane disruption similar to that caused by the parent toxin, L1AD3 promotes extensive and unusually rapid apoptosis in leukemic Tโ€cells without making the pla

Unspecific activation of caspases during
โœ Karina L. Johnson; David R. Grubb; Alfons Lawen ๐Ÿ“‚ Article ๐Ÿ“… 1999 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 171 KB ๐Ÿ‘ 2 views

Caspases have been implicated in the induction of apoptosis in most systems studied. The importance of caspases for apoptosis was further investigated using the system of didemnin B-induced apoptosis. We found that benzyloxycarbonyl-VAD-fluoromethylketone, a general caspase inhibitor, inhibits didem