Polypeptide Synthesis in Toluene‐Treated Lymphocytes

Normal human lymphocytes stimulated by phytohemagglutinin P, and other mammalian cells were rendered permeable to macromolecules such as poly(U) and proteins, by treatment with a low concentration of toluene. Under this condition, poly(U) translation was more efficient in the permeabilized cells tha...

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Autor principal: BURRONE, O.R.
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Acceso en línea:http://hdl.handle.net/20.500.12110/paper_00142956_v86_n2_p439_BURRONE
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spelling todo:paper_00142956_v86_n2_p439_BURRONE2023-10-03T14:11:59Z Polypeptide Synthesis in Toluene‐Treated Lymphocytes BURRONE, O.R. adenosine diphosphate adenosine triphosphate creatine kinase creatine phosphate guanosine triphosphate nuclease phenylalanine phytohemagglutinin p polypeptide polyuridylic acid radioisotope toluene in vitro study lymphocyte membrane permeability pharmacokinetics phenylalanine c 14 protein synthesis staphylococcus aureus uridine c 14 Animal Carcinoma, Ehrlich Tumor Comparative Study Human Lymphocytes Magnesium Peptide Synthesis Phenylalanine Poly U Ribonucleases Ribosomes Staphylococcus aureus Toluene Uridine Normal human lymphocytes stimulated by phytohemagglutinin P, and other mammalian cells were rendered permeable to macromolecules such as poly(U) and proteins, by treatment with a low concentration of toluene. Under this condition, poly(U) translation was more efficient in the permeabilized cells than in 10000 ×g extracts. Such a process occurs inside the treated cells as demonstrated by the fact that [14C]uridine‐labelled ribosomes remain associated with the toluene‐treated lymphocytes even after incubation at 37 °C. A nuclease from Staphylococcus aureus was able to penetrate the permeabilized cells and to break the polysome‐bound endogenous messenger RNA. However, the protein‐synthesizing machinery inside the toluene‐treated lymphocytes was unaffected by the nuclease, as demonstrated by the unimpairement of polyphenylalanine synthesis when poly(U) was added after the preincubation with the enzyme. These results suggest that the toluene treatment can be considered as an important tool for the study of the synthesis of macromolecules and its regulation in eukaryotic cells. Copyright © 1978, Wiley Blackwell. All rights reserved JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00142956_v86_n2_p439_BURRONE
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic adenosine diphosphate
adenosine triphosphate
creatine kinase
creatine phosphate
guanosine triphosphate
nuclease
phenylalanine
phytohemagglutinin p
polypeptide
polyuridylic acid
radioisotope
toluene
in vitro study
lymphocyte
membrane permeability
pharmacokinetics
phenylalanine c 14
protein synthesis
staphylococcus aureus
uridine c 14
Animal
Carcinoma, Ehrlich Tumor
Comparative Study
Human
Lymphocytes
Magnesium
Peptide Synthesis
Phenylalanine
Poly U
Ribonucleases
Ribosomes
Staphylococcus aureus
Toluene
Uridine
spellingShingle adenosine diphosphate
adenosine triphosphate
creatine kinase
creatine phosphate
guanosine triphosphate
nuclease
phenylalanine
phytohemagglutinin p
polypeptide
polyuridylic acid
radioisotope
toluene
in vitro study
lymphocyte
membrane permeability
pharmacokinetics
phenylalanine c 14
protein synthesis
staphylococcus aureus
uridine c 14
Animal
Carcinoma, Ehrlich Tumor
Comparative Study
Human
Lymphocytes
Magnesium
Peptide Synthesis
Phenylalanine
Poly U
Ribonucleases
Ribosomes
Staphylococcus aureus
Toluene
Uridine
BURRONE, O.R.
Polypeptide Synthesis in Toluene‐Treated Lymphocytes
topic_facet adenosine diphosphate
adenosine triphosphate
creatine kinase
creatine phosphate
guanosine triphosphate
nuclease
phenylalanine
phytohemagglutinin p
polypeptide
polyuridylic acid
radioisotope
toluene
in vitro study
lymphocyte
membrane permeability
pharmacokinetics
phenylalanine c 14
protein synthesis
staphylococcus aureus
uridine c 14
Animal
Carcinoma, Ehrlich Tumor
Comparative Study
Human
Lymphocytes
Magnesium
Peptide Synthesis
Phenylalanine
Poly U
Ribonucleases
Ribosomes
Staphylococcus aureus
Toluene
Uridine
description Normal human lymphocytes stimulated by phytohemagglutinin P, and other mammalian cells were rendered permeable to macromolecules such as poly(U) and proteins, by treatment with a low concentration of toluene. Under this condition, poly(U) translation was more efficient in the permeabilized cells than in 10000 ×g extracts. Such a process occurs inside the treated cells as demonstrated by the fact that [14C]uridine‐labelled ribosomes remain associated with the toluene‐treated lymphocytes even after incubation at 37 °C. A nuclease from Staphylococcus aureus was able to penetrate the permeabilized cells and to break the polysome‐bound endogenous messenger RNA. However, the protein‐synthesizing machinery inside the toluene‐treated lymphocytes was unaffected by the nuclease, as demonstrated by the unimpairement of polyphenylalanine synthesis when poly(U) was added after the preincubation with the enzyme. These results suggest that the toluene treatment can be considered as an important tool for the study of the synthesis of macromolecules and its regulation in eukaryotic cells. Copyright © 1978, Wiley Blackwell. All rights reserved
format JOUR
author BURRONE, O.R.
author_facet BURRONE, O.R.
author_sort BURRONE, O.R.
title Polypeptide Synthesis in Toluene‐Treated Lymphocytes
title_short Polypeptide Synthesis in Toluene‐Treated Lymphocytes
title_full Polypeptide Synthesis in Toluene‐Treated Lymphocytes
title_fullStr Polypeptide Synthesis in Toluene‐Treated Lymphocytes
title_full_unstemmed Polypeptide Synthesis in Toluene‐Treated Lymphocytes
title_sort polypeptide synthesis in toluene‐treated lymphocytes
url http://hdl.handle.net/20.500.12110/paper_00142956_v86_n2_p439_BURRONE
work_keys_str_mv AT burroneor polypeptidesynthesisintoluenetreatedlymphocytes
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