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Inteins as Biomolecular Switches : = Applications in Drug Discovery, Protein Purification, and Stress Response.

紀錄類型:	書目-語言資料,手稿 : Monograph/item
正題名/作者:	Inteins as Biomolecular Switches :/
其他題名:	Applications in Drug Discovery, Protein Purification, and Stress Response.
作者:	Pearson, C. Seth.
面頁冊數:	1 online resource (102 pages)
附註:	Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
Contained By:	Dissertation Abstracts International79-12B(E).
標題:	Chemical engineering. -
電子資源:	click for full text (PQDT)
ISBN:	9780438206229

Inteins as Biomolecular Switches : = Applications in Drug Discovery, Protein Purification, and Stress Response.
Pearson, C. Seth.

Inteins as Biomolecular Switches :Applications in Drug Discovery, Protein Purification, and Stress Response. - 1 online resource (102 pages)

Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.

Thesis (Ph.D.)--Rensselaer Polytechnic Institute, 2018.

Includes bibliographical references

Inteins are protein elements that autocatalytically excise themselves from a host protein in a process called protein splicing. The two flanking sequences of the host protein, called the N- and C-exteins, are subsequently ligated with a native peptide bond, resulting in a mature protein.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2018

Mode of access: World Wide Web

ISBN: 9780438206229Subjects--Topical Terms:

555952
Chemical engineering.
Index Terms--Genre/Form:

554714
Electronic books.

Inteins as Biomolecular Switches : = Applications in Drug Discovery, Protein Purification, and Stress Response.
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245 1 0 $a Inteins as Biomolecular Switches : $b Applications in Drug Discovery, Protein Purification, and Stress Response.
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500 $a Source: Dissertation Abstracts International, Volume: 79-12(E), Section: B.
500 $a Advisers: Georges Belfort; Marlene Belfort.
502 $a Thesis (Ph.D.)--Rensselaer Polytechnic Institute, 2018.
504 $a Includes bibliographical references
520 $a Inteins are protein elements that autocatalytically excise themselves from a host protein in a process called protein splicing. The two flanking sequences of the host protein, called the N- and C-exteins, are subsequently ligated with a native peptide bond, resulting in a mature protein.
520 $a During this process, the intein breaks two peptide bonds and forms a third. Taking advantage of the intein's ability to catalyze these reactions, both within the natural host as well as in vitro for biotechnological applications, provides an attractive opportunity. Implicit in effective utilization is an ability to control when, and if, catalysis occurs. Because inteins require no cofactors and have evolved an exquisite spatial and temporal coordination between the various peptide- making and -breaking reactions, achieving such control is not trivial. The work presented here aims to investigate how intein activity can be controlled in several disparate contexts.
520 $a Our work focuses on two of the three inteins found in the human pathogen Mycobacterium tuberculosis (Mtu), RecA and SufB. The intein-interrupted proteins are important for the viability of Mtu. Preventing intein excision, and thus the formation of important functional proteins, suggests that in vivo intein inhibition may be used as an anti-mycobacterial strategy. Building upon previous work with the chemotherapeutic cisplatin, we demonstrated potent in vitro inhibition of the RecA intein with novel cisplatin analogs using a fluorescent split-GFP assay. We also provided the structure of an intein-Pt co-crystal containing a platinum adduct at each catalytic cysteine, and calculate the binding kinetics using NMR. Perhaps most interestingly, we showed that the cisplatin ligands required for DNA binding are not present when bound to the intein, suggesting that less cross-reactive, and therefore less toxic, cisplatin analogs may be identified.
520 $a Turning to methods of control for in vitro applications, we introduced a mutation in Mtu RecA that causes the intein to spontaneously form a thiazoline ring at the N-terminal splicing junction. While present, the thiazoline ring prevents any further intein chemistry. We provided the first crystallographic evidence at 1.54 A resolution of this aberrant thiazoline chemistry in an intein. The crystal structure provides evidence for the existence of a tetrahedral intermediate resulting from nucleophilic attack by Cys1 on the adjacent extein residue carbonyl carbon. Additionally, the mutation that results in the thiazoline ring suggests that a highly conserved B-block Thr plays a pivotal role not only in "spring-loading" the scissile N-terminal peptide bond, but also in orienting the resulting tetrahedral intermediate for resolution into a thioester required for splicing, giving insight into the splicing mechanism. We demonstrated the stability of the thiazoline ring at neutral pH as well as sensitivity to hydrolytic opening of the ring under acidic conditions and increased temperature using mass spectrometry. A pH cycling strategy to induce N-terminal cleavage is provided, which may be of interest for biotechnological applications requiring a splicing activity switch such as single-step affinity-based purifications.
520 $a The final aspect of our work is based on the intriguing hypothesis that inteins are not simply parasitic elements, but offer a beneficial protein-level control of host protein function. We demonstrated that Mtu SufB activity is inhibited in vivo by oxidizing agents and copper ions, stressors to which the mature host protein is exquisitely sensitive. We provided evidence using ICP-MS and SDS-PAGE gel shift assays that suggest that the inhibition by copper ions is not direct, but rather part of a redox control mechanism involving oxidation of the catalytic cysteines. Further work to test this hypothesis must be performed and several lines of experimentation are proposed.
520 $a Overall, this work investigates strategies for controlling inteins in the realms of drug development, protein purification, and host regulation and stress response.
533 $a Electronic reproduction. $b Ann Arbor, Mich. : $c ProQuest, $d 2018
538 $a Mode of access: World Wide Web
650 4 $a Chemical engineering. $3 555952
650 4 $a Biochemistry. $3 582831
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710 2 $a Rensselaer Polytechnic Institute. $b Chemical Engineering. $3 1148535
773 0 $t Dissertation Abstracts International $g 79-12B(E).
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10683071 $z click for full text (PQDT)