Publication Date:
1999-09-08
Description:
Delivery of therapeutic proteins into tissues and across the blood-brain barrier is severely limited by the size and biochemical properties of the proteins. Here it is shown that intraperitoneal injection of the 120-kilodalton beta-galactosidase protein, fused to the protein transduction domain from the human immunodeficiency virus TAT protein, results in delivery of the biologically active fusion protein to all tissues in mice, including the brain. These results open new possibilities for direct delivery of proteins into patients in the context of protein therapy, as well as for epigenetic experimentation with model organisms.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Schwarze, S R -- Ho, A -- Vocero-Akbani, A -- Dowdy, S F -- New York, N.Y. -- Science. 1999 Sep 3;285(5433):1569-72.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Howard Hughes Medical Institute and Department of Pathology, Washington University School of Medicine, St. Louis, MO 63110, USA.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/10477521" target="_blank"〉PubMed〈/a〉
Keywords:
Animals
;
Blood-Brain Barrier
;
Brain/metabolism
;
Cell Membrane/metabolism
;
Drug Carriers
;
*Drug Delivery Systems
;
Fluorescein-5-isothiocyanate
;
Gene Products, tat/administration & dosage/*metabolism
;
Humans
;
Injections, Intraperitoneal
;
Jurkat Cells
;
Lipid Bilayers
;
Mice
;
Mice, Inbred C57BL
;
Microscopy, Confocal
;
Microscopy, Fluorescence
;
Muscle, Skeletal/metabolism
;
Recombinant Fusion Proteins/administration & dosage/*metabolism
;
Spleen/metabolism
;
Tissue Distribution
;
Tumor Cells, Cultured
;
beta-Galactosidase/administration & dosage/*metabolism
Print ISSN:
0036-8075
Electronic ISSN:
1095-9203
Topics:
Biology
,
Chemistry and Pharmacology
,
Computer Science
,
Medicine
,
Natural Sciences in General
,
Physics
