Theoretical studies of enzymic reactions: Dielectric, electrostatic and steric stabilization of the carbonium ion in the reaction of lysozyme

碳离子 溶菌酶 位阻效应 化学 电介质 离子 胞壁酶 光化学 计算化学 有机化学 材料科学 生物化学 光电子学
作者
Arieh Warshel,Michael Levitt
出处
期刊:Journal of Molecular Biology [Elsevier BV]
卷期号:103 (2): 227-249 被引量:4449
标识
DOI:10.1016/0022-2836(76)90311-9
摘要

Abstract A general method for detailed study of enzymic reactions is presented. The method considers the complete enzyme-substrate complex together with the surrounding solvent and evaluates all the different quantum mechanical and classical energy factors that can affect the reaction pathway. These factors include the quantum mechanical energies associated with bond cleavage and charge redistribution of the substrate and the classical energies of steric and electrostatic interactions between the substrate and the enzyme. The electrostatic polarization of the enzyme atoms and the orientation of the dipoles of the surrounding water molecules is simulated by a microscopic dielectric model. The solvation energy resulting from this polarization is considerable and must be included in any realistic calculation of chemical reactions involving anything more than an isolated molecule in vacuo . Without it, acidic groups can never become ionized and the charge distribution on the substrate will not be reasonable. The same dielectric model can also be used to study the reaction of the substrate in solution. In this way the reaction in solution can be compared with the enzymic reaction. In this paper we study the stability of the carbonium ion intermediate formed in the cleavage of a glycosidic bond by lysozyme. It is found that electrostatic stabilization is an important factor in increasing the rate of the reaction step that leads to the formation of the carbonium ion intermediate. Steric factors, such as the strain of the substrate on binding to lysozyme, do not seem to contribute significantly.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
Hello应助东是东南的东采纳,获得10
1秒前
李自律发布了新的文献求助10
2秒前
他有篮完成签到 ,获得积分10
2秒前
小马甲应助ttt123采纳,获得10
2秒前
339完成签到,获得积分10
3秒前
大意的不斜完成签到,获得积分10
4秒前
5秒前
5秒前
5秒前
6秒前
6秒前
一只白色的小鸡仔完成签到,获得积分10
6秒前
7秒前
科研通AI2S应助文艺的冬卉采纳,获得10
7秒前
7秒前
8秒前
8秒前
9秒前
Zoe_Zhang发布了新的文献求助10
9秒前
10秒前
11秒前
psyYang发布了新的文献求助10
11秒前
鲤鱼雨泽发布了新的文献求助10
11秒前
NexusExplorer应助eko采纳,获得10
12秒前
耍酷的玉米关注了科研通微信公众号
12秒前
今天是周六六完成签到 ,获得积分10
12秒前
深情安青应助1号采纳,获得10
12秒前
天下无双发布了新的文献求助10
12秒前
王升亮完成签到,获得积分20
12秒前
邓木发布了新的文献求助10
12秒前
14秒前
善良未来完成签到,获得积分10
15秒前
Hello应助吔94采纳,获得10
15秒前
皇上嗳完成签到,获得积分10
16秒前
16秒前
Orange应助旷意采纳,获得10
17秒前
17秒前
沿海地带应助加油的小白采纳,获得10
18秒前
是多少完成签到,获得积分10
19秒前
Rex发布了新的文献求助10
19秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
Electrode Potentials 550
REAL-WORLD EFFICACY AND GENOMIC LANDSCAPE OF POLATUZUMA VEDOTIN-BASED FIRST-LINE THERAPY IN DIFFUSE LARGE B-CELL LYMPHOMA: A FOCUS ON TP53 MUTATIONS AND TREATMENT RESPONSE 500
Handbook of Luminescence Dating 500
Safety Pharmacology 500
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6956205
求助须知:如何正确求助?哪些是违规求助? 8639709
关于积分的说明 18321082
捐赠科研通 6401881
什么是DOI,文献DOI怎么找? 3083951
关于科研通互助平台的介绍 2130779
邀请新用户注册赠送积分活动 2060706