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Ultraviolet photodissociation circular dichroism spectroscopy of protonated L-phenylalanyl-L-alanine in a cryogenic ion trap.
Yoo, Il Tae; Eun, Han Jun; Min, Ahreum; Jeon, Chang Wook; Jeong, Jinho; Heo, Jiyoung; Kim, Nam Joon.
Afiliación
  • Yoo IT; Department of Chemistry, Chungbuk National University, Chungbuk 28644, Korea. namjkim@chungbuk.ac.kr.
  • Eun HJ; Department of Chemistry, Chungbuk National University, Chungbuk 28644, Korea. namjkim@chungbuk.ac.kr.
  • Min A; Department of Chemistry (BK21 +) and Research Institute of Natural Science, Gyeongsang National University, Jinju 52828, Korea.
  • Jeon CW; Department of Chemistry, Chungbuk National University, Chungbuk 28644, Korea. namjkim@chungbuk.ac.kr.
  • Jeong J; Department of Chemistry, Chungbuk National University, Chungbuk 28644, Korea. namjkim@chungbuk.ac.kr.
  • Heo J; Department of Green Chemical Engineering, Sangmyung University, Chungnam 31066, Korea.
  • Kim NJ; Department of Chemistry, Chungbuk National University, Chungbuk 28644, Korea. namjkim@chungbuk.ac.kr.
Phys Chem Chem Phys ; 23(42): 24180-24186, 2021 Nov 03.
Article en En | MEDLINE | ID: mdl-34676382
ABSTRACT
We obtained ultraviolet photodissociation (UVPD) circular dichroism (CD) spectra of protonated L-phenylalanyl-L-alanine (L-H+PheAla) near the origin band of the S0-S1 transition using cryogenic ion spectroscopy. Infrared (IR) ion-dip, IR-UV hole burning (HB) and UV-UV HB spectra showed that L-H+PheAla existed as two different conformers in a cryogenic ion trap, and they had nearly identical peptide backbones but different conformations in the Phe side chain. The UVPD CD spectra revealed that the two conformers had opposite CD signs and significantly different CD magnitudes from each other. These results demonstrate that the CD value of L-H+PheAla near the origin band is strongly influenced by the conformation of the Phe side chain.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dipéptidos Idioma: En Revista: Phys Chem Chem Phys Asunto de la revista: BIOFISICA / QUIMICA Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Dipéptidos Idioma: En Revista: Phys Chem Chem Phys Asunto de la revista: BIOFISICA / QUIMICA Año: 2021 Tipo del documento: Article