Improve Research Reproducibility A Bio-protocol resource

PS
Piyali Saha
  • Post-Doc, Stanford University
研究方向
  • Biochemistry

Piyali Saha

个人信息

教育背景

PhD, Indian Institute of Science, 2014

实验室信息

Suzanne Pfeffer lab

研究方向

Cholesterol trafficking mechanism, Molecular Biology, Cell Biology, Biochemistry, Protein engineering, protein purification and characterization

发表论文

1.Li X*, Saha P*, Li J*, Blobel G, Pfeffer SR. Clues to the mechanism of cholesterol transfer from the structure of NPC1 middle lumenal domain bound to NPC2. Proc Natl Acad Sci U S A. (2016) 113, 10079-84.
2. Li J*, Deffieu MS*, Lee PL*, Saha P, Pfeffer SR. Glycosylation inhibition reduces cholesterol accumulation in NPC1 protein-deficient cells. Proc Natl Acad Sci U SA. (2015) 112, 14876-81.
3.Saha P*, Bhattacharyya S*, Kesavardhana S*, Miranda ER, Ali PS, Sharma D, Varadarajan R “Designed cyclic permutants of HIV-1 gp120: implications for envelope trimer structure and immunogen design”, Biochemistry (2012) 51, 1836-1847.
4. Saha P*, Barua B*, Bhattacharyya S, Balamurali MM, Schief WR, Baker D, Varadarajan R “Design and characterization of stabilized derivatives of human CD4D12 and CD4D1”, Biochemistry (2011) 50, 7891-7900.
5. Hu X, Saha P, Chen X, Kim D, Devarasetty M, Varadarajan R, Jin MM. Cell surface assembly of HIV gp41 six-helix bundles for facile, quantitative measurements of hetero-oligomeric interactions. J Am Chem Soc. (2012) 134, 14642-14645.
6. Rathore U, Saha P, Kesavardhana S, Kumar AA, Datta R, Devanarayanan S, Das R, Mascola JR, Varadarajan R. Glycosylation of the core of the HIV-1 envelope subunit protein gp120 is not required for native trimer formation or viral infectivity. J Biol Chem. (2017), 292, 10197-10219.
*Equal contribution