How do substrates enter and products exit the buried active site of cytochrome P450cam? 2. Steered molecular dynamics and adiabatic mapping of substrate pathways

Citation
Sk. Ludemann et al., How do substrates enter and products exit the buried active site of cytochrome P450cam? 2. Steered molecular dynamics and adiabatic mapping of substrate pathways, J MOL BIOL, 303(5), 2000, pp. 813-830
Citations number
39
Categorie Soggetti
Molecular Biology & Genetics
Journal title
JOURNAL OF MOLECULAR BIOLOGY
ISSN journal
00222836 → ACNP
Volume
303
Issue
5
Year of publication
2000
Pages
813 - 830
Database
ISI
SICI code
0022-2836(20001110)303:5<813:HDSEAP>2.0.ZU;2-M
Abstract
Three possible channels by which substrates and products can exit from the buried active site of cytochrome P450cam have been identified by means of r andom expulsion molecular dynamics simulations. In the investigation descri bed here, we computed estimates of the relative probabilities of ligand pas sage through the three channels using steered molecular dynamics and adiaba tic mapping. For comparison, the same techniques are also applied to invest igate substrate egress from cytochrome P450-BM3. The channel in cytochrome P450cam, for which there is the most supporting evidence from experiments ( which we name pathway 2a), is computed to be the most probable ligand exit channel. It has the smallest computed unbinding work and force. For this ch annel, the ligand exits between the F/G loop and the B' helix. Two mechanis tically distinct, but energetically similar routes through this channel wer e observed, showing that multiple pathways along one channel are possible. The probability of ligand exit via the next most probable channel (pathway 3), which is located between the I helix and the F and G helices, is estima ted to be less than 1/10 of the probability of exit along pathway 2a. Low-f requency modes of the protein extracted from an essential dynamics analysis of a 1 ns duration molecular dynamics simulation of cytochrome P450cam wit h camphor bound, support the opening of pathway 2a on a longer timescale. O n longer timescales, it is therefore expected that this pathway becomes mor e dominant than estimated from the present computations. (C) 2000 Academic Press.