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蛋白质中二级结构的(SSE)程序检测方案

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Introduction The multivariate SSE program can be used to analyze sets of CD data. A large number of samples can be automatically measured and efficiently analyzed using the high-throughput circular dichroism (HDX) system and multivariate SSE program. Keywords: Secondary structure estimation, Multiple samples, HTCD, HDX Sequence Optical constants are automatically calculated in the multivariate SSE program after imputing parameters

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Application Note sc CD-0008 Secondary structure estimation (SSE) program of multiple samples Introduction The multivariate SSE program can be used to analyze sets of CD data. A large number of samples can beautomatically measured and efficiently analyzed using the high-throughput circular dichroism (HDX) systemand multivariate SSE program. Keywords: Secondary structure estimation, Multiple samples, HTCD, HDX Sequence Optical constants are automatically calculated in the multivariate SSE program after imputing parametersas the path length and mean residue molar concentration. 1.63 1 58 Fig. 1 Specifying path length and mean residue molar concentration s.c CD-0008 CD Spectra Measurement 20C Pathlength:1 mmConcentration: 0.2 mg/mlTemp.:Wavelength:260-185 nmScan speed: 100 nm/minResponse:2 secData interval:0.1 nmBandwidth: l nm Accumulation: 2 Measurement time: 90 sec. per sample Fig. 2 CD spectra of eight proteins Lysozyme: Cytochrome C: Concanavalin A: b-Lactoglobulin: Trypsin Inhibitor: Ribonuclease A: Human Serum Albumin: Hemoglobin: Secondary Structure Estimation In table 1, the results of secondary structure estimation of eight proteins conducted using the PLS methodon CD spectra are compared with the results of X-ray crystallography. CD-0008 File Name Creation Date Sample name Helix Sheet Turn Other 1 O:¥..¥2011 2011/10/2512:25 Lyz 42.8% 0.4% 24.4% 32.4% 2 C:¥..¥2011 2011/10/25 12:25 Cytc 42.6% 3.1% 18.1% 36.2% 3 C:¥..¥2011 2011/10/2512:25 ConA 5.1% 44.6% 13.9% 36.4% 4 C:¥.¥2011 2011/10/2512:25 S-Lactoglobulin 17.8% 35.5% 12.3% 34.4% 5 C:¥.¥2011 2011/10/25 12:26 Trypsin Inhibitor 13.9% 25.3% 17.3% 43.5% 6 O:¥¥2011 2011/10/2512:26 RNaseA 21.5% 14.7% 22.4% 41.4% 7 C:¥..¥2011 2011/10/25 12:26 HSA 66.8% 1.3% 8.2% 23.7% 8 C:¥..¥2011 2011/10/25 12:27 Hb 61.1% 0.0% 18.0% 20.9% Fig. 3 Results using multivariate SSE program Table1 Comparison with X-ray crystallography Sample name Helix (%) Sheet (%) Turn (%) Other (%) Reference Lysozyme (Lyz) PLS 42.8 0.4 24.4 32.4 X-ray 41 4 19 35 1 Cytochrome C (CytC) PLS 42.6 3.1 18.1 36.2 X-ray 42 8 9 42 1 Concanavalin A (ConA) PLS 5.1 44.6 13.9 36.4 X-ray 2 36 12 49 1 B-Lactoglobulin PLS 17.8 35.5 12.3 34.4 X-ray 13 34 13 41 1 Trypsin Inhibitor PLS 13.9 25.3 17.3 43.5 X-ray 2 33 10 55 2 Ribonuclease A (RNaseA) PLS 21.5 14.7 22.4 41.4 X-ray 22 19 11 48 1 Human Serum Albumin (HSA) PLS 66.8 1.3 8.2 23.7 X-ray 72 0 8 20 2 Hemoglobin (Hb) PLS 61.1 0 18 20.9 X-ray 75 0 10 15 1 Helix: a-helix + 310-helix, Sheet: b-strand, Turn: turns, Other: rest References (1) W. Curtis Johnson, PROTEINS: Structure, Function, and Genetics, 35, 307-312,(1999) (2) PROTEIN DATA BANK: Trypsin inhibitor:1ba7 (DSSP), HAS: 1bm0 (DSSP) copyrightOJASCO CorporationJASCO INTERNATIONAL CO.,LTD-Sennin-cho -chome, Hachioji, Tokyo Japan IntroductionThe multivariate SSE program can be used to analyze sets of CD data. A large number of samples can beautomatically measured and efficiently analyzed using the high-throughput circular dichroism (HDX) system

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