An Ab Initio Analysis of Charge Redistribution upon Isomerization of Retinal in Rhodopsin and Bacteriorhodopsin

نویسندگان

  • BRITTANY CORN
  • SVETLANA A. MALINOVSKAYA
چکیده

In the framework of quantum-chemical methods (RHF, MP2, and DFT), we study the reaction of photoinduced isomerization of biological molecules—retinal in rhodopsin (Rh) and bacteriorhodopsin (BRh)—the key intermediates in the vision process. The charge redistribution in the retinal chromophore of these biological molecules as the mechanism of the photoinduced isomerization is investigated. The results of the Mulliken, Löwdin, Natural Bond, and ESP population analyses are compared and validated. We demonstrate that the isomerization reaction is accompanied by the substantial charge relocation within the isomerization region with the electron localization on C11 for the retinal in Rh and C14 for the retinal in BRh. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem 109: 3131–3141, 2009

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Quantum Chemistry: Molecular Dynamics Study of the Dark-Adaptation Process in Bacteriorhodopsin

Molecular dynamics simulations and quantum chemistry calculations have been combined to describe the dark adaptation in bacteriorhodopsin (bR). The process involves the reversible thermally activated transformation of retinal from an all-trans to a 13-cis,15-syn configuration. The potential surface governing the thermal isomerization of retinal around two (13-14, 15-N) double bonds has been det...

متن کامل

Molecular dynamics simulation of bacteriorhodopsin's photoisomerization using ab initio forces for the excited chromophore.

Retinal proteins are photoreceptors found in many living organisms. They possess a common chromophore, retinal, that upon absorption of light isomerizes and thereby triggers biological functions ranging from light energy conversion to phototaxis and vision. The photoisomerization of retinal is extremely fast, highly selective inside the protein matrix, and characterized through optimal sensitiv...

متن کامل

Microsecond atomic force sensing of protein conformational dynamics: implications for the primary light-induced events in bacteriorhodopsin.

In this paper a new atomic force sensing technique is presented for dynamically probing conformational changes in proteins. The method is applied to the light-induced changes in the membrane-bound proton pump bacteriorhodopsin (bR). The microsecond time-resolution of the method, as presently implemented, covers many of the intermediates of the bR photocycle which is well characterized by spectr...

متن کامل

Pii: S0166-1280(00)00410-3

Ab initio complete active space SCF calculations have been carried out to investigate the first excited electronic state of a retinal protonated Schiff base analog: all-trans-3,7-dimethylnona-2,4,6,8-tetraenmethylimminium cation. This model of the retinal chromophore in bacteriorhodopsin includes five conjugated double bonds as well as both pertinent backbone methyl groups. The excited state mi...

متن کامل

A theoretical study of benzaldehyde derivatives as tyrosinase inhibitors using Ab initio calculated NQCC parameters

Tyrosinase is a multifunctional copper-containing enzyme. It can catalyze two distinct reactions of melanin synthesis and benzaldehyde derivatives, which are potential tyrosinase inhibitors.  To find the relationships between charge distributions of benzaldehyde and their pharmaceutical behavior, the present study aimed at investigating nuclear quadrupole coupling constants of quadrupolare nucl...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2009