Baroresistant buffer mixtures for biochemical analyses

被引:48
作者
Quinlan, RJ [1 ]
Reinhart, GD [1 ]
机构
[1] Texas A&M Univ, Dept Biochem & Biophys, College Stn, TX 77843 USA
关键词
high hydrostatic pressure; pH; buffers;
D O I
10.1016/j.ab.2005.03.002
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Hydrostatic pressure is a useful tool in the study of varied fields such as protein aggregation, association, folding, ligand binding, and allostery. Application of pressure can have a significant effect on the pK(a) values of buffers commonly used for biochemical analysis. Consequently, cationic buffers, rather than neutral ones, are generally used to minimize pH effects; however, even with these buffers, the change in pH over 3 kbar may be consequential in highly pH-sensitive biochemical systems. Using fluorescence-based assays, we have systematically examined the effects of pressure on various buffers in the neutral pH range. We show that many commonly used cationic and Good's buffers increase in pH with pressure on the order of 0.1 to 0.3 pH units/kbar, in agreement with other published values. Carboxylates and phosphate decrease in pH to a similar extent. Buffer mixtures, composed of both cationic and carboxylate or phosphate components, are shown to be an order of magnitude less pressure sensitive than the individual component buffers. Using various relative concentrations of Tris and either phosphate, tricarballylate (1,2,3-propanetricarboxylate), or CDA (1,1-cyclohexane diacetate) at pH values between 7 and 8 yields baroresistant buffer mixtures. Buffer mixtures can be optimized for a specific pH, and a list of mixtures is presented for general laboratory use. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:69 / 76
页数:8
相关论文
共 40 条
[1]
PH-sensitive fluorescent dye as probe for proton uptake in photosynthetic reaction centers [J].
Agostiano, A ;
Mavelli, F ;
Milano, F ;
Giotta, L ;
Trotta, M ;
Nagy, L ;
Maroti, P .
BIOELECTROCHEMISTRY, 2004, 63 (1-2) :125-128
[2]
Pressure-induced perturbation of apomyoglobin structure: Fluorescence studies on native and acidic compact forms [J].
Bismuto, E ;
Sirangelo, I ;
Irace, G ;
Gratton, E .
BIOCHEMISTRY, 1996, 35 (04) :1173-1178
[3]
Effects of high pressure on meat: A review [J].
Cheftel, JC ;
Culioli, J .
MEAT SCIENCE, 1997, 46 (03) :211-236
[4]
Pressure inactivation kinetics of phage λ cI 857 [J].
Chen, HQ ;
Joerger, RD ;
Kingsley, DH ;
Hoover, DG .
JOURNAL OF FOOD PROTECTION, 2004, 67 (03) :505-511
[5]
Reversible stalling of transcription elongation complexes by high pressure [J].
Erijman, L ;
Clegg, RM .
BIOPHYSICAL JOURNAL, 1998, 75 (01) :453-462
[6]
HYDROGEN-ION BUFFERS FOR BIOLOGICAL-RESEARCH [J].
FERGUSON, WJ ;
BRAUNSCHWEIGER, KI ;
BRAUNSCHWEIGER, WR ;
SMITH, JR ;
MCCORMICK, JJ ;
WASMANN, CC ;
JARVIS, NP ;
BELL, DH ;
GOOD, NE .
ANALYTICAL BIOCHEMISTRY, 1980, 104 (02) :300-310
[7]
Foguel D, 1999, BIOTECHNOL BIOENG, V63, P552, DOI 10.1002/(SICI)1097-0290(19990605)63:5<552::AID-BIT5>3.0.CO
[8]
2-8
[9]
ROLE OF ENTROPIC INTERACTIONS IN VIRAL CAPSIDS - SINGLE AMINO-ACID SUBSTITUTIONS IN P22-BACTERIOPHAGE COAT PROTEIN RESULTING IN LOSS OF CAPSID STABILITY [J].
FOGUEL, D ;
TESCHKE, CM ;
PREVELIGE, PE ;
SILVA, JL .
BIOCHEMISTRY, 1995, 34 (04) :1120-1126
[10]
Good N E, 1972, Methods Enzymol, V24, P53