본문

서브메뉴

Structural Characterization of Microbial Pathogenesis: From Viruses to Parasites.
내용보기
Structural Characterization of Microbial Pathogenesis: From Viruses to Parasites.
자료유형  
 학위논문
Control Number  
0017164086
International Standard Book Number  
9798384080893
Dewey Decimal Classification Number  
576
Main Entry-Personal Name  
Stevens, Alexander.
Publication, Distribution, etc. (Imprint  
[S.l.] : University of California, Los Angeles., 2024
Publication, Distribution, etc. (Imprint  
Ann Arbor : ProQuest Dissertations & Theses, 2024
Physical Description  
211 p.
General Note  
Source: Dissertations Abstracts International, Volume: 86-03, Section: B.
General Note  
Includes supplementary digital materials.
General Note  
Advisor: Zhou, Hong;Rodriguez, Jose A.
Dissertation Note  
Thesis (Ph.D.)--University of California, Los Angeles, 2024.
Summary, Etc.  
요약Diseases caused by pathogenic microbes impose a substantial economic and public health burden on the world. Advancements in cryogenic electron microscopy (cryoEM) have revolutionized our ability to describe the atomic structures driving microbial pathogenesis, while eliminating artefacts introduced by classical structure methods. CryoEM improves both the biological context of these structures and broadens the scope of structural investigations to include large and dynamic complexes, where subtle differences can yield insights critical to combating these microbes.I began my thesis research by leveraging recent advancements in cryoEM image processing to address gaps in our understanding of the assembly and replication of double stranded RNA (dsRNA) viruses. We began with the study of a dsRNA virus with minimal genomic complexity, which lacks the capacity for intercellular infection. The resulting 3.6 A structure of the viral capsid informs us on the essential features required for dsRNA virus replication. We next turned to a more complex dsRNA virus, Aquareovirus (ARV), which poses a serious threat to aquaculture. By resolving the asymmetric structure of ARV capsid core-an intermediate state of the replication process-to 3.3 A, we could use the subtle differences between the complete and core particles to suggest a mechanism that explains the previously observed phenomenon of transcriptional inhibition in the complete particle. Our findings in both viruses deepen our understanding of viral replication in dsRNA viruses.Following this, we used cryoEM structures of the human cytomegalovirus (HCMV) capsid to guide the rational design of mutants targeting the protein-protein interface between the HCMV specific tegument protein, pp150, and the capsid. This structure guided mutagenesis allowed us to identify the potential mechanism of pp150 nuclear import and discover an attenuating mutation that slowed viral replication. Interestingly, this reduced replication rate did not compromise virion formation, suggesting such a mutation in clinical strains, may slow replication sufficiently for use as a vaccine strain, without affecting the virus's antigenic profile.Lastly, we applied cryoEM to cytoskeletal elements from the common genitourinary parasite T. vaginalis (Tv). As Tv pathogenicity relies upon the multifunctional, motile flagella, we aim to characterize the flagellar cytoskeleton, namely the doublet microtubules of the axoneme. In doing so, we identified the minimally complex arrangement of microtubule inner proteins (MIPs) that facilitate motility through the viscous environment of the host genitourinary tract. Furthermore, we identified a Novel MIP Tv-specific protein as a potential drug target.This work demonstrates the versatility of cryoEM to resolve new high-resolution structures, identify novel drug targets, and guide the rational design of mutants to probe protein-protein interactions and inform on the mechanisms of pathogenesis.
Subject Added Entry-Topical Term  
Microbiology.
Subject Added Entry-Topical Term  
Molecular biology.
Subject Added Entry-Topical Term  
Pathology.
Subject Added Entry-Topical Term  
Biochemistry.
Subject Added Entry-Topical Term  
Parasitology.
Subject Added Entry-Topical Term  
Virology.
Index Term-Uncontrolled  
Cryogenic electron microscopy
Index Term-Uncontrolled  
Herpesviruses
Index Term-Uncontrolled  
Pathogenesis
Index Term-Uncontrolled  
Structural biology
Index Term-Uncontrolled  
Trichomonas vaginalis
Added Entry-Corporate Name  
University of California, Los Angeles Biochemistry Molecular and Structural Biology 0090
Host Item Entry  
Dissertations Abstracts International. 86-03B.
Electronic Location and Access  
로그인을 한후 보실 수 있는 자료입니다.
Control Number  
joongbu:656327
신착도서 더보기
최근 3년간 통계입니다.

소장정보

  • 예약
  • 캠퍼스간 도서대출
  • 서가에 없는 책 신고
  • 나의폴더
소장자료
등록번호 청구기호 소장처 대출가능여부 대출정보
TQ0032449 T   원문자료 열람가능/출력가능 열람가능/출력가능
마이폴더 부재도서신고

* 대출중인 자료에 한하여 예약이 가능합니다. 예약을 원하시면 예약버튼을 클릭하십시오.

해당 도서를 다른 이용자가 함께 대출한 도서

관련도서

관련 인기도서

도서위치