4.5 Article

Including Rebinding Reactions in Well-Mixed Models of Distributive Biochemical Reactions

期刊

BIOPHYSICAL JOURNAL
卷 111, 期 10, 页码 2317-2326

出版社

CELL PRESS
DOI: 10.1016/j.bpj.2016.10.008

关键词

-

资金

  1. NSF grant [DMS-RTG 1148230, DMS 1122297]
  2. Division Of Mathematical Sciences
  3. Direct For Mathematical & Physical Scien [1148230, 1515130] Funding Source: National Science Foundation
  4. Division Of Mathematical Sciences
  5. Direct For Mathematical & Physical Scien [1122297] Funding Source: National Science Foundation

向作者/读者索取更多资源

The behavior of biochemical reactions requiring repeated enzymatic substrate modification depends critically on whether the enzymes act processively or distributively. Whereas processive enzymes bind only once to a substrate before carrying out a sequence of modifications, distributive enzymes release the substrate after each modification and thus require repeated bindings. Recent experimental and computational studies have revealed that distributive enzymes can act processively due to rapid rebindings (so-called quasi-processivity). In this study, we derive an analytical estimate of the probability of rapid rebinding and show that well-mixed ordinary differential equation models can use this probability to quantitatively replicate the behavior of spatial models. Importantly, rebinding requires that connections be added to the well-mixed reaction network; merely modifying rate constants is insufficient. We then use these well-mixed models to suggest experiments to 1) detect quasi-processivity and 2) test the theory. Finally, we show that rapid rebindings drastically alter the reaction's Michaelis-Menten rate equations.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.5
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据