APPLICATIONS OF GRAPH-THEORY TO ENZYME-KINETICS AND PROTEIN FOLDING KINETICS - STEADY AND NON-STEADY-STATE SYSTEMS

被引:217
作者
CHOU, KC
机构
[1] Computational Chemistry, Upjohn Research Laboratories, Kalamazoo
关键词
Cycle; Directed graph; Loop; Path; Phase concentration; Product-annihilating cycle; Product-creating cycle; Sink; Spanning in-tree; Transientconcentrat;
D O I
10.1016/0301-4622(90)80056-D
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
Graphic methods have proved to be very useful in enzyme kinetics, as reflected in both raising the efficiency of performing calculations and aiding in the analysis of catalytic mechanisms. The kinetic relations among protein folding states are very similar to those between enzyme-catalyzed species. Therefore, it should be equally useful to provide a visually intuitive relation between kinetic calculations and folding mechanisms for protein folding kinetics, as manifested by the graphic rules in enzyme kinetics. It can actually be anticipated that, due to increasing interest in protein folding, the graphic method will become an important tool in folding kinetics as well. Based on the recent progress made in graphic methods of enzyme kinetics, in this review four graphic rules are summarized, which can be used to deal with protein folding systems as well as enzyme-catalyzed systems. Rules 1-3 are established for deriving the kinetic equations for steady-state processes and Rule 4 for those in the case o on-steady-state processes. In comparison with conventional graphic methods, which can only be applied to a steady-state system, the current rules have the following advantages: (1) Complicated and tedious calculations can be greatly simplified. (2) A lot of wasted labor can be turned away. (3) Final results can be double-checked by a formula provided in each of the graphic rules. (4) Transient kinetic systems can also be treated. The mathematical proof of Rules 1-4 is given in appendices A-D, respectively. © 1990.
引用
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页码:1 / 24
页数:24
相关论文
共 32 条
[1]  
AINSLIE GR, 1972, J BIOL CHEM, V247, P7088
[2]   SLIDE-RULE FOR DERIVING RATE EQUATIONS OF ENZYME CATALYZED REACTIONS WITH UNBRANCHED MECHANISMS [J].
AINSWORTH, S .
JOURNAL OF THEORETICAL BIOLOGY, 1974, 44 (01) :161-165
[3]  
BEYER WH, 1988, CRC HDB MATH SCI, P544
[4]   ANALYTICAL DESCRIPTION OF THE EFFECTS OF MODIFIERS AND OF ENZYME MULTIVALENCY UPON THE STEADY STATE CATALYZED REACTION RATE [J].
BOTTS, J ;
MORALES, M .
TRANSACTIONS OF THE FARADAY SOCIETY, 1953, 49 (06) :696-707
[5]  
CHA S, 1968, J BIOL CHEM, V243, P820
[6]  
CHOU KC, 1980, EUR J BIOCHEM, V113, P195
[7]   GRAPHICAL RULES FOR ENZYME-CATALYZED RATE LAWS [J].
CHOU, KC ;
FORSEN, S .
BIOCHEMICAL JOURNAL, 1980, 187 (03) :829-835
[8]   2 NEW SCHEMATIC RULES FOR RATE LAWS OF ENZYME-CATALYZED REACTIONS [J].
CHOU, KC .
JOURNAL OF THEORETICAL BIOLOGY, 1981, 89 (04) :581-592
[9]   GRAPHICAL RULES FOR NON-STEADY STATE ENZYME-KINETICS [J].
CHOU, KC ;
LIU, WM .
JOURNAL OF THEORETICAL BIOLOGY, 1981, 91 (04) :637-654
[10]  
CHOU KC, 1979, SCI SINICA, V22, P341