Solute uptake through general porins

被引:96
作者
Delcour, AH [1 ]
机构
[1] Univ Houston, Dept Biol & Biochem, Houston, TX 77204 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2003年 / 8卷
关键词
outer membrane; porin; channel; bacteria; electrophysiology; permeability; antibiotic; review;
D O I
10.2741/1132
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
General diffusion porins are among the few membrane proteins that have been thoroughly investigated by many techniques, including X-ray crystallography, AFM microscopy, computer modeling, electrophysiology and biochemistry. This had led to a good understanding of the process of solute transport per se. However, other aspects of porin function remain enigmatic, such as the molecular basis and physiological relevance of many regulatory processes. After summarizing the most salient structural features, the review provides a description of the techniques used for the functional study of porins. The process of solute transport is presented on the basis of structure-function relationship and modeling studies. Three aspects of regulation are discussed: voltage-dependence, pH sensitivity and modulation by polycations and polyanions. The review ends with a perspective on future porin research, to be targeted at a molecular understanding of the regulatory processes, the deciphering of the physiological context in which these processes take place, and rational drug design.
引用
收藏
页码:D1055 / D1071
页数:17
相关论文
共 102 条
[41]   Spermidine-preferential uptake system in Escherichia coli - Identification of amino acids involved in polyamine binding in PotD protein [J].
Kashiwagi, K ;
Pistocchi, R ;
Shibuya, S ;
Sugiyama, S ;
Morikawa, K ;
Igarashi, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (21) :12205-12208
[42]  
KREUSCH A, 1994, PROTEIN SCI, V3, P58
[43]   Transport of maltodextrins through maltoporin: A single-channel study [J].
Kullman, L ;
Winterhalter, M ;
Bezrukov, SM .
BIOPHYSICAL JOURNAL, 2002, 82 (02) :803-812
[44]   CHARACTERIZATION OF CHANNELS INDUCED IN PLANAR BILAYER-MEMBRANES BY DETERGENT SOLUBILIZED ESCHERICHIA-COLI PORINS [J].
LAKEY, JH ;
WATTS, JP ;
LEA, EJA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1985, 817 (02) :208-216
[45]   OMPC MUTANTS WHICH ALLOW GROWTH ON MALTODEXTRINS SHOW INCREASED CHANNEL SIZE AND GREATER VOLTAGE SENSITIVITY [J].
LAKEY, JH ;
LEA, EJA ;
PATTUS, F .
FEBS LETTERS, 1991, 278 (01) :31-34
[46]   THE VOLTAGE-DEPENDENT ACTIVITY OF ESCHERICHIA-COLI PORINS IN DIFFERENT PLANAR BILAYER RECONSTITUTIONS [J].
LAKEY, JH ;
PATTUS, F .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 186 (1-2) :303-308
[47]  
LIU N, 1999, THESIS U HOUSTON
[48]   Inhibitory effect of acidic pH on OmpC porin: wild-type and mutant studies [J].
Liu, NZ ;
Delcour, AH .
FEBS LETTERS, 1998, 434 (1-2) :160-164
[49]   Effects of pore mutations and permeant ion concentration on the spontaneous gating activity of OmpC porin [J].
Liu, NZ ;
Samartzidou, H ;
Lee, KW ;
Briggs, JM ;
Delcour, AH .
PROTEIN ENGINEERING, 2000, 13 (07) :491-500
[50]   The spontaneous gating activity of OmpC porin is affected by mutations of a putative hydrogen bond network or of a salt bridge between the L3 loop and the barrel [J].
Liu, NZ ;
Delcour, AH .
PROTEIN ENGINEERING, 1998, 11 (09) :797-802