東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Chromatographic measurement of prote...

Teske, Christopher Alan.

FindBook

Google Book

Amazon

博客來

Chromatographic measurement of protein-protein interactions.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Chromatographic measurement of protein-protein interactions./
作者:	Teske, Christopher Alan.
面頁冊數:	97 p.
附註:	Source: Dissertation Abstracts International, Volume: 65-02, Section: B, page: 0891.
Contained By:	Dissertation Abstracts International65-02B.
標題:	Engineering, Chemical. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3121725
ISBN:	0496690760

Chromatographic measurement of protein-protein interactions.
Teske, Christopher Alan.

Chromatographic measurement of protein-protein interactions. - 97 p.

Source: Dissertation Abstracts International, Volume: 65-02, Section: B, page: 0891.

Thesis (Ph.D.)--University of California, Berkeley, 2003.

Understanding how solution conditions affect protein-protein interactions is useful for designing and optimizing protein separation processes such as salt-induced protein precipitation. Further, attractive protein-protein interactions can lead to protein aggregation which has been linked to Alzheimer's and Parkinson's disease. Information for interactions between unlike proteins is necessary for predicting phase equilibria for multi-component protein solutions commonly encountered in protein-purification processes. Common methods for measuring protein-protein interactions include static light scattering, membrane osmometry and equilibrium sedimentation. These methods suffer from the disadvantage of requiring a relatively large amount of protein. Further, with these techniques it is difficult to measure directly interactions between unlike proteins. Chromatographic measurement of protein-protein interactions provides a possible method to overcome these disadvantages.

ISBN: 0496690760Subjects--Topical Terms:

1018531
Engineering, Chemical.

Chromatographic measurement of protein-protein interactions.
LDR:03475nmm 2200325 4500 001 1844228
005 20051017073447.5
008 130614s2003 eng d
020 $a 0496690760
035 $a (UnM)AAI3121725
035 $a AAI3121725
040 $a UnM $c UnM
100 1 $a Teske, Christopher Alan. $3 1932425
245 1 0 $a Chromatographic measurement of protein-protein interactions.
300 $a 97 p.
500 $a Source: Dissertation Abstracts International, Volume: 65-02, Section: B, page: 0891.
500 $a Chairs: Harvey W. Blanch; John M. Prausnitz.
502 $a Thesis (Ph.D.)--University of California, Berkeley, 2003.
520 $a Understanding how solution conditions affect protein-protein interactions is useful for designing and optimizing protein separation processes such as salt-induced protein precipitation. Further, attractive protein-protein interactions can lead to protein aggregation which has been linked to Alzheimer's and Parkinson's disease. Information for interactions between unlike proteins is necessary for predicting phase equilibria for multi-component protein solutions commonly encountered in protein-purification processes. Common methods for measuring protein-protein interactions include static light scattering, membrane osmometry and equilibrium sedimentation. These methods suffer from the disadvantage of requiring a relatively large amount of protein. Further, with these techniques it is difficult to measure directly interactions between unlike proteins. Chromatographic measurement of protein-protein interactions provides a possible method to overcome these disadvantages.
520 $a To measure protein-protein interactions chromatographically, one protein is immobilized on a porous stationary phase while a solution of the second protein passes through the column as the mobile phase. The retention time of the mobile protein (relative to that of a similarly-sized non-interacting tracer) provides a quantitative measure of the mobile-protein/immobile-protein interaction. Chromatographic measurement of protein-protein interactions requires significantly less protein than static light scattering or membrane osmometry and, in principle, can directly measure interactions between unlike proteins.
520 $a Using a standard liquid chromatograph, we have measured lysozyme-lysozyme interactions as a function of aqueous solution conditions (pH, ionic strength, salt identity). All measurements were at 25°C. Results are reported at pH 4 and 7 for sodium chloride (concentrations up to 1.7m) and ammonium sulfate (concentrations up to 1.0m). Osmotic second virial coefficients are calculated from our chromatographic results and compared with those from static light scattering. For reduction of chromatographic data, it is necessary to consider multibody interactions between a mobile lysozyme molecule and many immobilized molecules on the solid support. A model is constructed to account for multibody interactions assuming pairwise additivity and using a potential of mean force that contains hard sphere, electrostatic, and square-well contributions. (Abstract shortened by UMI.)
590 $a School code: 0028.
650 4 $a Engineering, Chemical. $3 1018531
650 4 $a Biophysics, General. $3 1019105
650 4 $a Chemistry, Biochemistry. $3 1017722
690 $a 0542
690 $a 0786
690 $a 0487
710 2 0 $a University of California, Berkeley. $3 687832
773 0 $t Dissertation Abstracts International $g 65-02B.
790 1 0 $a Blanch, Harvey W., $e advisor
790 1 0 $a Prausnitz, John M., $e advisor
790 $a 0028
791 $a Ph.D.
792 $a 2003
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3121725