TY - JOUR
T1 - Metalloids
T2 - essential, beneficial or toxic? Major intrinsic proteins sort it out
AU - Bienert, Gerd P.
AU - Schüssler, Manuela D.
AU - Jahn, Thomas P.
N1 - Funding Information:
We thank Enzo Lombi and Angela Feechan for critical reading of the manuscript. Work in our laboratory was supported by the Danish Ministry of Science, Technology and Innovation (Grant 23–03–0103 to T.P.J.).
PY - 2008/1
Y1 - 2008/1
N2 - Major intrinsic proteins (MIPs) are a family of selective membrane channels comprising water-channelling aquaporins and glycerol-channelling aquaglyceroporins. Recently, several MIPs within all domains of life were shown to facilitate the diffusion of reduced and non-charged species of the metalloids silicon, boron, arsenic and antimony. Metalloids encompass a group of biologically important elements ranging from the essential to the highly toxic. Consequently, all organisms require efficient membrane transport systems to control the exchange of metalloids with the environment. Recent genetic evidence has demonstrated a crucial role for specific MIPs in metalloid homeostasis. We propose that specific MIPs represent an ancient and indispensable transport mechanism for metalloids, which suggests that they could be potential pharmacological targets.
AB - Major intrinsic proteins (MIPs) are a family of selective membrane channels comprising water-channelling aquaporins and glycerol-channelling aquaglyceroporins. Recently, several MIPs within all domains of life were shown to facilitate the diffusion of reduced and non-charged species of the metalloids silicon, boron, arsenic and antimony. Metalloids encompass a group of biologically important elements ranging from the essential to the highly toxic. Consequently, all organisms require efficient membrane transport systems to control the exchange of metalloids with the environment. Recent genetic evidence has demonstrated a crucial role for specific MIPs in metalloid homeostasis. We propose that specific MIPs represent an ancient and indispensable transport mechanism for metalloids, which suggests that they could be potential pharmacological targets.
UR - http://www.scopus.com/inward/record.url?scp=37749006472&partnerID=8YFLogxK
U2 - 10.1016/j.tibs.2007.10.004
DO - 10.1016/j.tibs.2007.10.004
M3 - Review article
C2 - 18068370
AN - SCOPUS:37749006472
SN - 0968-0004
VL - 33
SP - 20
EP - 26
JO - Trends in Biochemical Sciences
JF - Trends in Biochemical Sciences
IS - 1
ER -