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 到查詢結果 [ null ]

切換: 標籤 | MARC模式 | ISBD

Designing Proteins and Peptides for ...

Gosavi, Pallavi M.

FindBook

Google Book

Amazon

博客來

Designing Proteins and Peptides for Catalysis, Biophysical Studies and Therapeutic Applications.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Designing Proteins and Peptides for Catalysis, Biophysical Studies and Therapeutic Applications./
作者:	Gosavi, Pallavi M.
出版者:	Ann Arbor : ProQuest Dissertations & Theses, : 2018,
面頁冊數:	250 p.
附註:	Source: Dissertations Abstracts International, Volume: 80-01, Section: B.
Contained By:	Dissertations Abstracts International80-01B.
標題:	Bioengineering. -
電子資源:	https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10744460
ISBN:	9780438101951

Designing Proteins and Peptides for Catalysis, Biophysical Studies and Therapeutic Applications.
Gosavi, Pallavi M.

Designing Proteins and Peptides for Catalysis, Biophysical Studies and Therapeutic Applications. - Ann Arbor : ProQuest Dissertations & Theses, 2018 - 250 p.

Source: Dissertations Abstracts International, Volume: 80-01, Section: B.

Thesis (Ph.D.)--Syracuse University, 2018.

This item must not be added to any third party search indexes.

Enzymes are large biomolecules which catalyze complex reactions with high selectivity and efficiency. The function of an enzyme depends on the unique three-dimensional structure dictated by the amino acid sequence. Understanding the evolutionary origin of enzyme's structure and function is pivotal for designing proteins/peptides with novel or enhanced function. Extensive research efforts in this field have led to successful strategies which combine sophisticated computational algorithm and high-throughput combinatorial techniques. These strategies have been used to develop peptides and proteins for biocatalysis, antibody therapeutics and drug delivery applications etc. In this work, we used a minimalistic approach with high-throughput screening to design efficient peptides and proteins with novel functions. In the initial study, we designed a library of short 7-residue peptides that self-assembled and catalyzed ester hydrolysis in presence of Zn II with activity at par with the natural enzyme by weight. Furthermore, self-assembly of these peptides in presence of CuII allowed us to create a catalyst for oxygen activation. Thus, we demonstrated that self-assembly of peptides can present an excellent tool to design catalyst for difficult chemical transformations. More importantly, this approach enables screening of multiple co-ordination spheres, simply by mixing different peptides. The ease with which we were able to develop these catalysts suggest that short peptide-assemblies might have served as intermediates in enzyme evolution. Additionally, we applied a minimalistic approach to design a catalyst for selective post translational modification. Strategic incorporation of single His residue at position 144 in a non-enzymatic eukaryotic protein calmodulin (CaM) introduced hydrolytic and acylase activity into the protein. The designed allosterically regulated acylase was capable of site selective acylation of Lys residues in CaM-binding peptides involved in regulation of various cellular processes. Moreover, this acylase can serve as a unique chemical biology tool to identify CaM-binding domains and elucidate structural interactions between CaM and its binding partner. In this work, we also demonstrated that introduction of an unnatural Trp analog, AzAla into peptides/proteins can allow monitoring of protein-protein interaction, protein folding and dynamics. The weak environmental dependence along with the sensitivity to weak intrinsic quenchers makes AzAla a unique fluorescent probe for such studies. Substitution of AzAla in place of Trp in M2 channel of influenza A enabled us to monitor the protonation state of His residues with minimum perturbation to function. Moreover, with the availability of technology to introduce AzAla translationally into proteins, we envision that AzAla will gain wide utility in biophysical studies. Lastly, we utilized a rational design approach to develop a peptide microbicide candidate for prevention of sexual transmission of HIV. HIV is a great public health challenge worldwide and effective strategies are required to stop the spread of this pandemic. Current antiretroviral therapy is successful; however, the approach is also susceptible to developing drug resistance. Recently, it was demonstrated that amyloid fibrils formed in semen called semen-induced enhancer of virus infection (SEVI) increased HIV infectivity by several-fold in vivo. In this work, we designed a peptide E-FK16 that selectively interacts with SEVI. Using E-FK16, we created a randomized library which would be screened using phage display to identify a peptide candidate with greater ability to interact with SEVI and thus prevent HIV transmission through SEVI. SEVI presents a unique target to develop microbicide for prevention of HIV transmission as this strategy does not target the viral machinery and hence it would be difficult for the virion to develop resistance.

ISBN: 9780438101951Subjects--Topical Terms:

657580
Bioengineering.
Subjects--Index Terms:

Biophysical studies

Designing Proteins and Peptides for Catalysis, Biophysical Studies and Therapeutic Applications.
LDR:05298nmm a2200409 4500 001 2275306
005 20210119090647.5
008 220723s2018 ||||||||||||||||| ||eng d
020 $a 9780438101951
035 $a (MiAaPQ)AAI10744460
035 $a (MiAaPQ)syr:11803
035 $a AAI10744460
040 $a MiAaPQ $c MiAaPQ
100 1 $a Gosavi, Pallavi M. $3 3553549
245 1 0 $a Designing Proteins and Peptides for Catalysis, Biophysical Studies and Therapeutic Applications.
260 1 $a Ann Arbor : $b ProQuest Dissertations & Theses, $c 2018
300 $a 250 p.
500 $a Source: Dissertations Abstracts International, Volume: 80-01, Section: B.
500 $a Publisher info.: Dissertation/Thesis.
500 $a Advisor: Korendovych, Ivan V.;Sweder, Kevin.
502 $a Thesis (Ph.D.)--Syracuse University, 2018.
506 $a This item must not be added to any third party search indexes.
506 $a This item must not be sold to any third party vendors.
520 $a Enzymes are large biomolecules which catalyze complex reactions with high selectivity and efficiency. The function of an enzyme depends on the unique three-dimensional structure dictated by the amino acid sequence. Understanding the evolutionary origin of enzyme's structure and function is pivotal for designing proteins/peptides with novel or enhanced function. Extensive research efforts in this field have led to successful strategies which combine sophisticated computational algorithm and high-throughput combinatorial techniques. These strategies have been used to develop peptides and proteins for biocatalysis, antibody therapeutics and drug delivery applications etc. In this work, we used a minimalistic approach with high-throughput screening to design efficient peptides and proteins with novel functions. In the initial study, we designed a library of short 7-residue peptides that self-assembled and catalyzed ester hydrolysis in presence of Zn II with activity at par with the natural enzyme by weight. Furthermore, self-assembly of these peptides in presence of CuII allowed us to create a catalyst for oxygen activation. Thus, we demonstrated that self-assembly of peptides can present an excellent tool to design catalyst for difficult chemical transformations. More importantly, this approach enables screening of multiple co-ordination spheres, simply by mixing different peptides. The ease with which we were able to develop these catalysts suggest that short peptide-assemblies might have served as intermediates in enzyme evolution. Additionally, we applied a minimalistic approach to design a catalyst for selective post translational modification. Strategic incorporation of single His residue at position 144 in a non-enzymatic eukaryotic protein calmodulin (CaM) introduced hydrolytic and acylase activity into the protein. The designed allosterically regulated acylase was capable of site selective acylation of Lys residues in CaM-binding peptides involved in regulation of various cellular processes. Moreover, this acylase can serve as a unique chemical biology tool to identify CaM-binding domains and elucidate structural interactions between CaM and its binding partner. In this work, we also demonstrated that introduction of an unnatural Trp analog, AzAla into peptides/proteins can allow monitoring of protein-protein interaction, protein folding and dynamics. The weak environmental dependence along with the sensitivity to weak intrinsic quenchers makes AzAla a unique fluorescent probe for such studies. Substitution of AzAla in place of Trp in M2 channel of influenza A enabled us to monitor the protonation state of His residues with minimum perturbation to function. Moreover, with the availability of technology to introduce AzAla translationally into proteins, we envision that AzAla will gain wide utility in biophysical studies. Lastly, we utilized a rational design approach to develop a peptide microbicide candidate for prevention of sexual transmission of HIV. HIV is a great public health challenge worldwide and effective strategies are required to stop the spread of this pandemic. Current antiretroviral therapy is successful; however, the approach is also susceptible to developing drug resistance. Recently, it was demonstrated that amyloid fibrils formed in semen called semen-induced enhancer of virus infection (SEVI) increased HIV infectivity by several-fold in vivo. In this work, we designed a peptide E-FK16 that selectively interacts with SEVI. Using E-FK16, we created a randomized library which would be screened using phage display to identify a peptide candidate with greater ability to interact with SEVI and thus prevent HIV transmission through SEVI. SEVI presents a unique target to develop microbicide for prevention of HIV transmission as this strategy does not target the viral machinery and hence it would be difficult for the virion to develop resistance.
590 $a School code: 0659.
650 4 $a Bioengineering. $3 657580
650 4 $a Biochemistry. $3 518028
650 4 $a Nanoscience. $3 587832
653 $a Biophysical studies
653 $a Catalysts
653 $a Peptides
653 $a Proteins
653 $a Therapeutic application
690 $a 0202
690 $a 0487
690 $a 0565
710 2 $a Syracuse University. $b Chemistry. $3 3428706
773 0 $t Dissertations Abstracts International $g 80-01B.
790 $a 0659
791 $a Ph.D.
792 $a 2018
793 $a English
856 4 0 $u https://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10744460