Enzymes without borders: Mobilizing substrates, delivering products

被引:61
作者
Forneris, Federico [1 ]
Mattevi, Andrea [1 ]
机构
[1] Univ Pavia, Dept Genet & Microbiol, I-27100 Pavia, Italy
关键词
D O I
10.1126/science.1151118
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 [理学]; 0710 [生物学]; 09 [农学];
摘要
Many cellular reactions involve both hydrophobic and hydrophilic molecules that reside within the chemically distinct environments defined by the phospholipid- based membranes and the aqueous lumens of cytoplasm and organelles. Enzymes performing this type of reaction are required to access a lipophilic substrate located in the membranes and to catalyze its reaction with a polar, water- soluble compound. Here, we explore the different binding strategies and chemical tricks that enzymes have developed to overcome this problem. These reactions can be catalyzed by integral membrane proteins that channel a hydrophilic molecule into their active site, as well as by water- soluble enzymes that are able to capture a lipophilic substrate from the phospholipid bilayer. Many chemical and biological aspects of this type of enzymology remain to be investigated and will require the integration of protein chemistry with membrane biology.
引用
收藏
页码:213 / 216
页数:4
相关论文
共 51 条
[1]
Crystal structure of a human membrane protein involved in cysteinyl leukotriene biosynthesis [J].
Ago, Hideo ;
Kanaoka, Yoshihide ;
Irikura, Daisuke ;
Lam, Bing K. ;
Shimamura, Tatsuro ;
Austen, K. Frank ;
Miyano, Masashi .
NATURE, 2007, 448 (7153) :609-U12
[2]
Cholesterol oxidase senses subtle changes in lipid bilayer structure [J].
Ahn, KW ;
Sampson, NS .
BIOCHEMISTRY, 2004, 43 (03) :827-836
[3]
Crystal structure of saposin B reveals a dimeric shell for lipid binding [J].
Ahn, VE ;
Faull, KF ;
Whitelegge, JP ;
Fluharty, AL ;
Privé, GG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (01) :38-43
[4]
Crystal structures of saposins A and C [J].
Ahn, Victoria E. ;
Leyko, Paul ;
Alattia, Jean-Rene ;
Chen, Lu ;
Prive, Gilbert G. .
PROTEIN SCIENCE, 2006, 15 (08) :1849-1857
[5]
A proposed time-resolved X-ray scattering approach to track local and global conformational changes in membrane transport proteins [J].
Andersson, Magnus ;
van der Spoel, David ;
Davidsson, Jan ;
Neutze, Richard .
STRUCTURE, 2008, 16 (01) :21-28
[6]
Interfacial enzymology:: The secreted phospholipase A2-paradigm [J].
Berg, OG ;
Gelb, MH ;
Tsai, MD ;
Jain, MK .
CHEMICAL REVIEWS, 2001, 101 (09) :2613-2653
[7]
The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[8]
Yeast acyl-CoA synthetases at the crossroads of fatty acid metabolism and regulation [J].
Black, Paul N. ;
DiRusso, Concetta C. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2007, 1771 (03) :286-298
[9]
Enzymology and molecular biology of glucocorticoid metabolism in humans [J].
Blum, A ;
Maser, E .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 75, 2003, 75 :173-216
[10]
Structural adaptations in a membrane enzyme that terminates endocannabinoid signaling [J].
Bracey, MH ;
Hanson, MA ;
Masuda, KR ;
Stevens, RC ;
Cravatt, BF .
SCIENCE, 2002, 298 (5599) :1793-1796