Summary

उपन्यास गुरुत्वीय फोर्स स्पेक्ट्रोमीटर का उपयोग करता है दिखाते खींचो और रेशेदार प्रोटीन उपाय

Published: March 19, 2011
doi:

Summary

इस एक कदम से कदम गाइड उद्देश्य, संचालन, और उपन्यास गुरुत्वाकर्षण बल स्पेक्ट्रोमीटर से प्रतिनिधि परिणाम दिखा है.

Abstract

The study of macromolecular structure has become critical to the elucidation of molecular mechanisms and function. There are several limited, but important bioinstruments capable of testing the force dependence of structural features in proteins. Scale has been a limiting parameter on how accurately researchers can peer into the nanomechanical world of molecules, such as nucleic acids, enzymes, and motor proteins that perform life-sustaining work. Atomic force microscopy (AFM) is well tuned to determine native structures of fibrous proteins with a distance resolution on par with electron microscopy. However, in AFM force studies, the forces are typically much higher than a single molecule might experience 1, 2. Optical traps (OT) are very good at determining the relative distance between the trapped beads and they can impart very small forces 3. However, they do not yield accurate absolute lengths of the molecules under study. Molecular simulations provide supportive information to such experiments, but are limited in the ability to handle the same large molecular sizes, long time frames, and convince some researchers in the absence of other supporting evidence2, 4.

The gravitational force spectrometer (GFS) fills a critical niche in the arsenal of an investigator by providing a unique combination of abilities. This instrument is capable of generating forces typically with 98% or better accuracy from the femtonewton range to the nanonewton range. The distance measurements currently are capable of resolving the absolute molecular length down to five nanometers, and relative bead pair separation distances with a precision similar to an optical trap. Also, the GFS can determine stretching or uncoiling where the force is near equilibrium, or provide a graded force to juxtapose against any measured structural changes. It is even possible to determine how many amino acid residues are involved in uncoiling events under physiological force loads 2. Unlike in other methods where there is extensive force calibration that must precede any assay, the GFS requires no such force calibration 5. By complementing the strengths of other methods, the GFS will bridge gaps in understanding the nanomechanics of vital proteins and other macromolecules.

Protocol

उपन्यास GFS विन्यास करने के लिए परिचय एक नियमित रूप से प्रकाश माइक्रोस्कोप, एक भूमध्य माउंट, एक कैमरा, और एक कंप्यूटर [चित्रा 1]: GFS कई आवश्यक घटक के होते हैं. सील प्रवाह सेल कक्ष है जो नमूना धारण भी G…

Discussion

जब एक डिजिटल thresholded प्रतिनिधित्व करने के लिए एक फिल्म में परिवर्तित, यह thresholded छवि के लिए वीडियो के हर फ्रेम में एक ही क्षेत्र को बनाए रखने के लिए महत्वपूर्ण है. क्योंकि एक मनका जोड़ी में मोतियों कदम एक दूसर?…

Disclosures

The authors have nothing to disclose.

Acknowledgements

इस सामग्री को अनुदान नंबर 0842736 के तहत राष्ट्रीय विज्ञान फाउंडेशन द्वारा समर्थित काम पर आधारित है.

Materials

Material Name Type Company Catalogue Number Comment
3-Aminopropyltriethoxysilane   Poly Sciences 919-30-2  
Acetone   Fisher Scientific A18P-4  
Pyridine   Sigma Aldrich 110-86-1  
Glutaraldehyde   Fisher Scientific G7776  
Glycine   Research Organics BP381-1  
Tris   Sigma 9682T  
Sodium azide   Amresco 71289  
BSA   Sigma Aldrich AMR-0332-100G  
NaCl   Sigma S7653  
EDTA   MSI E9884  
Nitrocellulose   Sigma 60443  
N-N Dimethyl Formamide   Extracted from Large New D4254  
Rabbit skeletal myosin II   Zealand White Rabbits (7-8) NA  
MF30 antibody (9-10)   Developmental Studies MF30  
MF20 antibody (6)   Hybridoma Bank MF20  
Lab microscope   Boreal WW57905M00  
Equatorial mount   Celestron CG-5  
Digital video cam   Sony XCDV60  
Caliper release   Cabelas IA-415482  
Compression spring   Jones Spring Co. 723  
Extension spring   Jones Spring Co. 770  
ImageJ   NIH NA  
Fire-i drivers & application   Unibrain 3.80  
Excel   Microsoft NA  

References

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  7. Godfrey, J. E., Harrington, W. F. Self-association in the myosin system at high ionic strength. I. Sensitivity of the interaction to pH and ionic environment. Biochemistry. 9, 886-893 (1970).
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Cite This Article
Dunn, J. W., Root, D. D. Demonstrating the Uses of the Novel Gravitational Force Spectrometer to Stretch and Measure Fibrous Proteins. J. Vis. Exp. (49), e2624, doi:10.3791/2624 (2011).

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