Origins of the sensitivity of molecular vibrations to electric fields: Carbonyl and nitrosyl stretches in model compounds and proteins

被引:132
作者
Park, ES [1 ]
Boxer, SG [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1021/jp0203043
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The vibrational Stark effect (VSE) is the effect of an electric field on the vibrational spectrum. Typically, the largest change induced by an electric field is the linear frequency shift whose sensitivity is known as the Stark tuning rate Deltamu, the magnitude and direction of Amu are measured by VSE spectroscopy. This can be used to calibrate the sensitivity of vibrational frequencies to local electrostatic fields in proteins. To be most useful, it is critical to obtain a sensitive probe that has a large Amu, and understanding the origins of Deltamu is required. The Stark tuning rate arises from two distinct origins: mechanical anharmonicity (Amu(anh)) and the change of the bond force constant because of the electronic polarizability (Deltamu(bond)), with Deltamu = Deltamu(anh) + Deltamu(bond.) These two origins were quantitatively investigated for carbonyl and nitrosyl stretches in model compounds and proteins by IR and VSE spectroscopy. The contribution of Amu(anh) was found to dominate Au for carbonyl stretches in acetone, methyl vinyl ketone, and 1-methyl-2-pyrrolidinone despite their different degrees of electron delocalization. In contrast, the presence of d-pi* back-bonding when CO is bound to the heme causes Deltamu(bond) to be more significant, giving rise to large variations in the Fe-CO and C-O stretch frequencies in heme protein variants such as myoglobin mutants, with a strong negative correlation between V-Fe-(CO) and (V) over barC-O. The back-bonding also increases Deltamu(anh) because of the enhanced effective charges on the CO oscillator. By comparison, the small variation in Fe-NO stretch frequency and the absence of a strong negative correlation between Fe-NO and N-O stretch frequencies for NO bound to the heme iron in myoglobin variants suggest that Deltamu(Fe-NO) is much smaller than Deltamu(Fe-CO), possibly because of less back-bonding in heme-NO complexes. Nevertheless, Deltamu(N-O) has approximately the same magnitude as Deltamu(C-O) when bound to heme. suggesting that the anharmonic effect on VSE is larger for the N-O stretch than that for C-O stretch.
引用
收藏
页码:5800 / 5806
页数:7
相关论文
共 41 条
[1]   A liquid nitrogen immersion cryostat for optical measurements [J].
Andrews, SS ;
Boxer, SG .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2000, 71 (09) :3567-3569
[2]   Vibrational Stark effects of nitriles II. Physical origins of stark effects from experiment and perturbation models [J].
Andrews, SS ;
Boxer, SG .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (03) :469-477
[3]   Vibrational stark effects of nitriles I. Methods and experimental results [J].
Andrews, SS ;
Boxer, SG .
JOURNAL OF PHYSICAL CHEMISTRY A, 2000, 104 (51) :11853-11863
[4]  
Antonini E., 1971, HEMOGLOBIN MYOGLOBIN
[5]   The determinants of pK(a)s in proteins [J].
Antosiewicz, J ;
McCammon, JA ;
Gilson, MK .
BIOCHEMISTRY, 1996, 35 (24) :7819-7833
[6]  
ATKINS PW, 1994, PHYSICAL CHEM
[7]   THE VIBRATIONAL STARK-EFFECT [J].
BISHOP, DM .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (04) :3179-3184
[8]   VIBRATIONAL STARK-EFFECT SPECTROSCOPY [J].
CHATTOPADHYAY, A ;
BOXER, SG .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1995, 117 (04) :1449-1450
[9]   A TEST OF THE ROLE OF ELECTROSTATIC INTERACTIONS IN DETERMINING THE CO STRETCH FREQUENCY IN CARBONMONOXYMYOGLOBIN [J].
DECATUR, SM ;
BOXER, SG .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 212 (01) :159-164
[10]   VIBRATIONAL SPECTRA AND ASSIGNMENT OF ACETONE ALPHAALPHAALPHA ACETONE-D3 AND ACETONE-D6 [J].
DELLEPIANE, G ;
OVEREND, J .
SPECTROCHIMICA ACTA, 1966, 22 (04) :593-+