TY - JOUR
T1 - Protein transduction
T2 - Unrestricted delivery into all cells?
AU - Schwarze, Steven R.
AU - Hruska, Keith A.
AU - Dowdy, Steven F.
PY - 2000/7/1
Y1 - 2000/7/1
N2 - Several proteins can traverse biological membranes through protein transduction. Small sections of these proteins (10-16 residues long) are responsible for this. Linking these domains covalently to compounds, peptides, antisense peptide nucleic acids or 40-nm iron beads, or as in-frame fusions with full-length proteins, lets them enter any cell type in a receptor- and transporter-independent fashion. Moreover, several of these fusions, introduced into mice, were delivered to all tissues, even crossing the blood-brain barrier. These domains thus might let us address new questions and even help in the treatment of human disease. Copyright (C) 2000 Elsevier Science Ltd.
AB - Several proteins can traverse biological membranes through protein transduction. Small sections of these proteins (10-16 residues long) are responsible for this. Linking these domains covalently to compounds, peptides, antisense peptide nucleic acids or 40-nm iron beads, or as in-frame fusions with full-length proteins, lets them enter any cell type in a receptor- and transporter-independent fashion. Moreover, several of these fusions, introduced into mice, were delivered to all tissues, even crossing the blood-brain barrier. These domains thus might let us address new questions and even help in the treatment of human disease. Copyright (C) 2000 Elsevier Science Ltd.
UR - http://www.scopus.com/inward/record.url?scp=0034237577&partnerID=8YFLogxK
U2 - 10.1016/S0962-8924(00)01771-2
DO - 10.1016/S0962-8924(00)01771-2
M3 - Review article
C2 - 10856932
AN - SCOPUS:0034237577
SN - 0962-8924
VL - 10
SP - 290
EP - 295
JO - Trends in Cell Biology
JF - Trends in Cell Biology
IS - 7
ER -