High-Throughput Large-Aperture Prism Prefilter for Ultraviolet Resonance Raman Spectroscopy

For the acquisition of high-quality ultraviolet resonance Raman spectra of strongly scattering samples such as membrane protein suspensions, an f/3.5 Littrow prism prefilter has been designed, built, and characterized. This prefilter has a Czerny–Turner configuration, and its focal length is 25 cm. The apex angle of the dispersive prism (20°) was chosen to provide maximum performance in the 220 to 240 nm range. The prism prefilter significantly reduced stray background due to Rayleigh scattering and visible fluorescence, while maintaining a low dispersion of 1300 cm−1/mm at 253 nm as well as a large f/3.5 aperture. The sharpness of the transmission edge (at 242 nm, the T = 0% to 95% transition occurs in 1.3 nm) quantitates its effectiveness as a sharp-cut Rayleigh scattering filter. The total throughput of the prefilter is ∼60% at 235 nm and ∼50% at 632.8 nm. The utility of this prefilter is demonstrated by obtaining high signal-to-noise resonance Raman spectra of bacteriorhodopsin in a purple membrane suspension with 239.5 nm excitation.

[1]  R A Mathies,et al.  Ultraviolet resonance Raman examination of the light-induced protein structural changes in rhodopsin activation. , 1997, Biochemistry.

[2]  H. Takeuchi,et al.  Ultraviolet resonance Raman evidence for the absence of tyrosinate in octopus rhodopsin and the participation of Trp residues in the transition to acid metarhodopsin , 1996, FEBS letters.

[3]  G. Thomas,et al.  Design and performance of an ultraviolet resonance Raman spectrometer for proteins and nucleic acids. , 1995, Biophysical journal.

[4]  Y. Mizutani,et al.  Ultraviolet Resonance Raman Studies of Quaternary Structure of Hemoglobin Using a Tryptophan 37 Mutant (*) , 1995, Journal of Biological Chemistry.

[5]  I. Harada,et al.  Utilization of a Prism Monochromator as a Sharp-Cut Bandpass Filter in Ultraviolet Raman Spectroscopy , 1993 .

[6]  Richard W. Bormett,et al.  UV Resonance Raman Spectroscopy Using a New cw Laser Source: Convenience and Experimental Simplicity , 1993 .

[7]  T. Kitagawa,et al.  A Novel Idea for Practical UV Resonance Raman Measurement with a Double Monochromator and its Application to Protein Structural Studies , 1992 .

[8]  R. Mathies,et al.  Time-resolved ultraviolet resonance Raman studies of protein structure: application to bacteriorhodopsin. , 1992, Biochemistry.

[9]  S. Subramaniam,et al.  Hemoglobin R.fwdarw.T structural dynamics from simultaneous monitoring of tyrosine and tryptophan time-resolved UV resonance Raman signals , 1992 .

[10]  R. L. Benson,et al.  Improvements in the Generation of Quasi-Continuous, Tunable Ultraviolet Excitation for Raman Spectroscopy: Applications to Drug/Nucleotide Interactions , 1992 .

[11]  T. Kitagawa Investigation of higher order structures of proteins by ultraviolet resonance Raman spectroscopy. , 1992, Progress in biophysics and molecular biology.

[12]  I. Harada,et al.  Ultraviolet resonance Raman spectroscopy of X—Proline bonds: A new marker band of hydrogen bonding at the imide CO site , 1990 .

[13]  T. Kitagawa,et al.  Time-resolved ultraviolet resonance Raman study of the photolysis of a carbomonoxyhemoglobin: relaxation of the globin structure , 1990 .

[14]  Sanford A. Asher,et al.  High-Repetition-Rate Excimer-Based UV Laser Excitation Source Avoids Saturation in Resonance Raman Measurements of Tyrosinate and Pyrene , 1987 .

[15]  I. Harada,et al.  Normal coordinate analysis of the indole ring , 1986 .

[16]  S. Asher,et al.  Development of a new UV resonance Raman spectrometer for the 217–400‐nm spectral region , 1983 .

[17]  E. Heller,et al.  Excited state geometry changes from preresonance Raman intensities: Isoprene and hexatriene , 1982 .

[18]  K. Rothschild,et al.  [76] Kinetic resonance raman spectroscopy of purple membrane using rotating sample , 1982 .

[19]  L. Ziegler,et al.  Resonance Raman scattering of benzene and benzene‐d6 with 212.8 nm excitation , 1981 .

[20]  R. Mathies,et al.  Raman spectroscopy with intensified vidicon detectors: A study of intact bovine lens proteins , 1978 .

[21]  D. Oesterhelt,et al.  Isolation of the cell membrane of Halobacterium halobium and its fractionation into red and purple membrane. , 1974, Methods in enzymology.

[22]  S. Rice,et al.  The design of optical spectrometers , 1969 .